We thank Ing. Duncan van Groen for programming the image analysis software (ImageGrabber) used in this study. Funding for this research has been provided by a VIDI grant from the Netherlands Organisation for Scientific Research (grant 016.136.372).

All animal experiments have been approved by the local animal care and ethical committee. The entire protocol from induction of anesthesia in the mouse until the end of the hyperinsulinemic-euglycemic clamp takes approximately 2 h.
1. Microsurgical Preparation
<ol>
	<li>Induce anesthesia along with analgesia in&#160;a male mouse weighing 20-25 g after a 14 h or overnight fasting with an intraperitoneal injection of a Fentanyl (0.31 mg/kg), Midazolam (6.25 mg/kg) and Acepromazine (6.25 mg/kg) (FMA anesthesia) and place it on a rectal-temperature-controlled homeothermic heating pad which maintains body temperature at 37 &#176;C.</li>
	<li>Disinfect the operation table and the equipment several times using an alcohol-based solution.</li>
	<li>Attach a 27 G needle to a 10 cm long polyethylene tube (PE-20) and attach the tube to a 4-way connector. Insert the needle in the tail vein and fixate it using tissue adhesive gel. This cannula will be used for infusion of microbubbles, insulin, glucose and anesthesia. 
	Note: Adding Heparin (5 U/mL) in sterile saline during the cannulation process to flush the tail vein (approximately 10 &#181;L) reduces the possibility of clogged cannulas.</li>
	<li>Throughout the surgical procedures and experimental protocols, maintain anesthesia by a continuous intravenous infusion of FMA anesthesia&#160;via the tail vein cannula at rate of 33.75 &#181;L/kg/min.</li>
	<li>Place the mouse with the ventral side up and fix the feet using a thermostable tape to expose the upper thigh area. Use a slight exorotation of the hip joint (hindlimb paws facing up) and a 40-60&#176; angle at the knee joint to standardize the stretch of the muscle at the adductor compartment of the thigh.</li>
	<li>Remove the hair at the groin and upper thigh areas bilaterally using a depilatory cream. Collect all the loose hair with a moist cotton swab.</li>
	<li>Place the mouse under a stereomicroscope and perform the following surgical steps using 10X to 16X magnification.</li>
	<li>Make a 2 cm incision using skin scissors running parallel to the inguinal ligament, just lateral to the abdominal curvature (Figure 1). Apply traction on the distal side of the incision distally using a bulldog clamp (Figure 1D). This will help to adjust the window as needed and help hold the paraffin oil (described in 1.12).</li>
	<li>Dissect the adipose tissue away from the abdominal wall. To avoid bleeding, gently separate the fat pad from the wall instead of dissecting directly through the pad. Gentle traction at the fat pad in the distal direction will facilitate the process (Figure 1C).</li>
	<li>Identify the femoral artery and follow it down to the first major branches (the epigastric artery and the gracilis artery) (Figure 2). The gracilis artery is the first major branch of the femoral artery running on the adductor magnus muscle and then runs deep to the gracilis muscle. The gracilis artery will be used for IVM.</li>
	<li>Identify the transparent deep fascia covering the muscles and the vessels. Using sharp forceps, pull the fascia upwards and cut it using a microscissor.</li>
	<li>Cover the exposed muscle with a drop (200 &#181;L) of medicinal liquid paraffin (room temperature, or pre-warmed to 37 &#176;C) to prevent the prepared tissue from drying out. Make sure that the oil drop does not leak away. Adjust the skin folds of the incision using the bulldog clamp to create a small cavity to hold the paraffin oil that bathes the vessels.</li>
	<li>Place the mouse under a previously calibrated microscope (16X optical magnification) in such a way that the gracilis artery is vertical on the computer screen. Attach the microscope to a camera and computer based analysis system that can extract the vessels&#39; diameter from the image data set. The diameter is the distance between the two luminal sides of the vessel. Continuous monitoring and measurement of the artery diameter is desirable.</li>
	<li>Place the light source at a sufficient distance (minimum 20 cm) from the hindlimb to reduce head conduction from the light.</li>
	<li>Apply prewarmed ultrasound transduction gel to the upper contralateral hindlimb. Place the ultrasound probe perpendicular to the long axis of the femur bone.</li>
	<li>Carefully adjust the angle and direction of the ultrasound probe to get a cross-sectional view of the adductor muscle group. Take care to keep the position of the ultrasound probe in relation to the mouse stable to keep the same imaging plane for baseline and hyperinsulinemic measurements.</li>
	<li>Let the mouse stabilize for 30 min. The diameter of the gracilis artery should be stable for 10 min before documenting the baseline diameter.</li>
</ol>
2. Baseline and Hyperinsulinemic Measurements
<ol>
	<li>Make sure that the baseline gracilis artery diameter is saved by the computer program used for the IVM.</li>
	<li>Prepare the microbubbles in advance as described35 and count with Coulter counter to a concentration of 2.5 x 109 bubbles/mL just before the experiment.</li>
	<li>As the microbubbles can only be viewed in the contrast-mode of the ultrasound machine, control the parameters which affect the image and the contrast data collected (described in 2.3.1) and use consistently during acquisition.
	<ol>
		<li>Use the following settings on the ultrasound machine: contrast gain at 35 decibels; the time gain compensation to OFF; Line Density to HIGH; Number of Focal Zones to WIDE; Transmit Power to 4%; Transmit Beam width to STANDARD; SV Gate to 4; Sensitivity to 1; Persistence to OFF. Level the location of Focal Zones to the center of the region of interest.</li>
	</ol>
	</li>
	<li>Save a short (5 s) clip. This will be used to calculate the background signal.</li>
	<li>Shake the vial containing the microbubbles by hand to have a uniform suspension. Start infusing the microbubbles using the tail vein cannula at a 5 &#181;L/min rate. Place the infusion tube on a vibrating vortex (200x per min) to maintain a uniform suspension of microbubbles.</li>
	<li>Allow 5 min of continuous infusion of microbubbles so that a steady-state level is reached. Proceed with obtaining the time-intensity curves of the bubbles using the microbubble destruct function (MBD) on the ultrasound machine at 5 min and at 10 min after the start of microbubbles infusion (Figure 3A). Take the average signal of these two measurements to get the baseline perfusion data.</li>
	<li>After obtaining the baseline data, start the hyperinsulinemic-euglycemic clamp as described34. Use the tail cannula (placed in 1.3) to administer the insulin and glucose (and anesthesia).
	<ol>
		<li>In short, induce a hyperinsulinemic state by introducing a 200 mU/kg insulin bolus followed by continuous insulin infusion (7.5 mU/kg/min) for 60 min. Use a variable infusion of 20% D-glucose to maintain euglycemia.</li>
		<li>Assess blood glucose from the tail vein every 5 min with a Glucose Monitoring Device, and maintain at 5 mM by adjusting the variable glucose infusion rate. Determine insulin sensitivity by averaging the mean glucose infusion rate during the last 30 min.</li>
	</ol>
	</li>
	<li>Make sure that the diameter of the gracilis artery is documented at the desired time periods (for example at 10, 30 and 60 min) of the start of the hyperinsulinemic-euglycemic clamp with the computer program.</li>
	<li>After 25 min and/or 55 min of the insulin clamp, start the second (hyperinsulinemic) CEUS measurement to document the MBV at 30 and/or 60 min, respectively. Follow the same steps described in 2.4 and 2.5. Detach and use the anesthesia port of the 4-way connector to infuse the microbubbles. Reattach the anesthesia tube after the end of the microbubbles infusion.</li>
	<li>After completion of IVM and the CEUS measurements 60 min after the start of insulin infusion, withdraw blood from the mouse by a heart puncture procedure for later analysis. This will also euthanize the mouse. Carefully dissect the gracilis and femoral arteries and store them for further desired experiments (for e.g., Western blots, Immunohistochemistry, ex vivo pressure myography experiments36,37,38).</li>
</ol>
3. Offline Analysis

NOTE: The analyses of IVM and CEUS measurements should be performed offline by a blinded investigator. CEUS offers the possibility to distinguish the microcirculation from larger vessels by temporarily destructing the microbubbles by high intensity ultrasound waves using the MBD function. The signal (measured in arbitrary units (a.u)) in larger vessels is restored quicker than those in the microcirculation because of the microbubbles speed in the corresponding vessels.
<ol>
	<li>Use an offline workstation or the software on the ultrasound machine to do the analyses.</li>
	<li>Draw a region of interests (ROI) to include the microcirculation. Draw a separate ROI to include the larger femoral vessels (Figure 3A).</li>
	<li>Duplicate the microcirculation&#39;s and larger vessels&#39; ROIs for the background, baseline and hyperinsulinemic measurements by using the ROI copy function built in the software.</li>
	<li>Subtract the intensity signal of the background measurement from the baseline and the hyperinsulinemic measurements.</li>
	<li>Divide the intensity signal of the microcirculation by the intensity signal of the femoral vessels. Baseline and hyperinsulinemic MBVs can now be compared.</li>
</ol>

Visual Sonics Inc. covered the open access fees, whereas the structure and content of the article remained the full responsibility of the authors.

We have developed a technique to simultaneously estimate insulin&#39;s vascular actions on the larger arteries (using IVM) and the skeletal muscle microcirculation (using CEUS). The critical steps for successful and reliable measurements are: 1) correctly exposing the gracilis artery without bleeding; 2) preventing leakage of the paraffin oil bathing the artery; 3) having a patent venous access (tail vein cannula) for infusion of vasoactive compounds (insulin) and contrast agent (microbubbles).
The study of microvascular dysfunction in muscle has been gaining attention in the context of obesity and insulin resistance14,25,39,40. The negative impact of obesity and insulin resistance on vascular function is manifested at different levels of the vascular tree. Henceforth, different approaches are required to assess these changes. The combined use of the IVM and CEUS techniques in the same mouse provides a powerful tool to quantify insulin&#39;s effects at different levels of the vasculature. IVM allows direct visualization and quantitative analysis of the resistance artery and CEUS allows for assessment of insulin-induced changes in muscle perfusion.
Studying the adductor muscle compartment has several advantages. The arteries are readily accessible and the superficial nature of the incision makes it possible to close the skin incision with a 5.0 absorbable sterile suture after the experiment is finished. The animals were injected subcutaneously with buprenorphine after the experiments as an analgesic at a dose of 0.1 mg/kg and allowed to recover in a warm environment. The mice tolerated the procedure very well and we experienced no loss of animals nor infections of the hindlimb in more than 35 animals studied. This makes it possible to follow-up or study the animals in a longitudinal fashion. The animals used in these experiments, however, were anesthetized using 1.8% inhaled isoflurane balanced with oxygen flowing at 0.4 L/min though an anesthesia mask. In contrast to isoflurane anesthesia41,42, FMA anesthesia does not disturb peripheral insulin sensitivity. A future plan is to study how well the mice recover from FMA anesthesia.
The adductor muscle compartment is also useful since various vasoactive compounds mediating local and downstream vascular effects can be evaluated. For example, topical application of these compounds to the target tissue is feasible using superfusion techniques28 or surgical manipulation and implantation of drug-eluting cuffs surrounding the vessels43. Furthermore, the gracilis artery can be isolated and studied in the pressure myograph. Our group and others have gathered substantial experimental evidence using the pressure myograph to document the effects of insulin and other vasoactive compounds on this artery ex vivo36,37,38.
A limitation inherent to the use of the IVM technique is the surgical exposition of the muscle and application of paraffin oil to stabilize the vessels. It is not clear whether these actions impact the native environment of the artery. However, Figure 3A shows that the baseline diameter of the gracilis artery bathed in paraffin oil does not change considerably. It has been also shown that mineral oil successfully inhibits the diffusion of oxygen, protecting the tissue from hyperoxic conditions44. Moreover, the oil helps to reduce the variation in the baseline diameter of the arteries. This is why we advocate to use paraffin oil and let the preparation rest for at least 30 min. Of note, the use of buffered saline instead of oil &#8211; or no oil at all &#8211; resulted in highly variable diameters and constriction of the vessel (data not shown). Moreover, at the end of the experiments, we isolated the gracilis arteries - bathed in paraffin oil - and tested their reactivity in the pressure myograph ex vivo. The paraffin oil-bathed arteries reacted similarly to control arteries when stimulated with insulin and acetylcholine (a vasodilator) (data not shown). The consistent insulin-induced vasodilation clearly shows that the IVM protocol described in this study produces reliable results.
The advantage of applying both techniques in the same mouse overcomes some of the intrinsic limitations of one technique by the other: CEUS estimates MBV in the undisturbed muscle in vivo, but individual vessels cannot be seen; IVM makes it possible to see individual vessels, albeit it cannot estimate MBV. A future plan is to utilize IVM microscopy of the cremaster muscle in combination with CEUS of the adductor muscle on the contralateral side. This modification can provide an estimate of the MBV (using CEUS) and a direct optical access to the capillaries (using IVM). The protocol can be further modified; the 4-way connector used for the tail cannula can be switched to a 5-way connector. By this, we can avoid detaching the anesthesia tube while performing the second CEUS measurement (described in point 2.9). In our experience, the mice tolerated the current protocol well. Another modification that can be made to this protocol is the insulin clamp rate used. We used 7.5 mU/kg/min clamp rate which is considered supra-physiological. Depending on the study, a lower insulin clamp rate (for example 3 mU/kg/min) can be used.
While we have found the described protocol reliable, there are specific limitations that need attention. There are situations when the measurement of the arterial diameter is not optimal. Executing the preparation steps requires some experience with the model. It is crucial that the paraffin oil does not leak from the vessel environment as supplementing it with new oil will disturb the vessel and change the diameter, making it necessary to let the artery rest for another 30 min. In addition, the reflection of the light (described in step 1.14 of the protocol) on the surface of the paraffin oil was sometimes too bright, making it difficult to view the artery. This can be counteracted by directing the light source so that the light falls at an angle to the paraffin oil surface and parallel to the artery.
In conclusion, the combination of IVM and CEUS techniques described in this study makes it possible to quantify different effects of insulin at different levels of the vasculature. IVM of the gracilis artery provides insight into the upstream vascular changes contributing to downstream microvascular perfusion measured using CEUS. We advocate the combination of several experimental techniques in the same mouse to better assess the vascular function.

In response to a rise in blood glucose level, the pancreas secretes insulin into the bloodstream where it is quickly distributed to its target tissues such as skeletal muscle, via resistance arteries and capillaries. Skeletal muscle is responsible for ~80% of postprandial glucose uptake1. The delivery of insulin to the skeletal muscle interstitium has been shown to be a rate limiting step for the metabolic actions of insulin that promote glucose disposal2,3,4. Within 10-15 min, insulin increases the capillary blood volume (microvascular recruitment), an effect that occurs before total blood flow increases5,6. Microvascular recruitment expands the endothelial surface area available for exchange of nutrients (and insulin)7,8. Insulin-mediated microvascular recruitment precedes and is independently associated with changes in skeletal muscle glucose uptake8,9. The effect of insulin on the vasculature has been termed &#39;vascular insulin sensitivity&#39;.
It has been shown that insulin-mediated microvascular recruitment and insulin-induced vasodilation are impaired in obese Zucker rats10,11. Moreover, lean mice with reduced capillary density display muscle insulin resistance12. In their influential work, Kubota et al. showed that impaired insulin signaling in endothelial cells caused reduction in insulin-induced microvascular&#160;recruitment, which reduced glucose uptake in skeletal muscle by approximately 40%13. These abnormalities in microvascular function do not only occur in muscle, but also in multiple other tissues and organs such as the heart, retina and kidney14,15,16. These examples and other studies17,18,19,20 suggest that vascular effects of insulin are an important mechanism in the (patho)physiology of insulin resistance and its complications.
While there is substantial evidence that insulin increases microvascular blood volume (MBV) in skeletal muscle5,6, the mechanisms by which this happens are not completely understood9. Endothelium-dependent vasodilation is essential in many aspects of vascular insulin sensitivity21,22,23 at different levels of the vasculature. Vascular insulin sensitivity can manifest itself by insulin-induced relaxation of resistance arteries and by relaxation of pre-capillary arterioles to increase the perfused microvascular exchange surface area7,24,25.
Intravital microscopy (IVM) has been used in a variety of tissue preparations including skinfold chambers of the mouse dorsum26, the mesentery of the mouse and rat27, models of limb ischemia in the mouse28 and the hamster cheek pouch29. Contrast-enhanced ultrasonography (CEUS) is another imaging technique that allows assessment of the microcirculation in cardiac30 as well as skeletal muscle31. It utilizes inert gas-filled microbubbles which behave rheologically as red blood cells and remain entirely within the vascular lumen. These microbubbles are infused intravenously at a constant rate to attain a steady state. A high energy ultrasound wave, then, can be used to destroy the microbubbles. The microbubbles&#39; replenishment speed in the region of interest (ROI) represents flow velocity (MFV). The total signal intensity of the contrast image represents the MBV. CEUS can be performed repeatedly (also in humans) and it has advanced the understanding of vascular dysfunction that occurs in insulin-resistant states (discussed in Barrett et al.32).
In the current study we describe a new technique for studying regulation of muscle perfusion, through simultaneous use of both IVM and CEUS. Here we focus on insulin&#39;s vascular actions in the adductor compartment of the mouse hindlimb. This compartment is one of the largest skeletal muscle groups in the mouse, enabling studies of local glucose uptake in a representative muscle. This compartment is ideal for IVM as the preparation and visualization of the arteries are readily accessible by a standardized surgical procedure28. Moreover, our own group and others have shown that CEUS can be used in this compartment33,34.
An advantage to the combined IVM and CEUS technique is the possibility to assess insulin&#39;s effect at the level of the larger arterioles (feed or resistance arteries) and the microcirculation (capillary beds) in the same muscle group. In addition, the simultaneous application of the two methods provides insight into the temporal action of insulin at the levels of the resistance arteries and microcirculation. This combined IVM and CEUS technique can also be implemented in other vascular biology fields. For example, the role of various proteins and certain pathophysiological conditions affecting the endothelium can be studied using knockout models. Moreover, both techniques can be used in one mouse at multiple time points reducing the time and cost of research.

<table><tbody><tr><td>C57BL/6 Mice</td><td>Charles river</td><td></td><td>Mice used were bred in-house</td></tr><tr><td>Vevo 2100 high-resolution ultrasound system</td><td>VisualSonics inc.</td><td></td><td></td></tr><tr><td>MS250 non-linear transducer</td><td>VisualSonics inc.</td><td></td><td></td></tr><tr><td>Vevo 2100 software</td><td>VisualSonics inc.</td><td></td><td></td></tr><tr><td>Ultrasound gel (Aquasonic 100, colourless)</td><td>CSP Medical</td><td>133-1009</td><td>Ultrasound gel used to transmit the ultrasound waves</td></tr><tr><td>Vortex</td><td>VWR international</td><td>58815-234</td><td></td></tr><tr><td>Heating pad&amp;nbsp;</td><td>Pantlab</td><td></td><td></td></tr><tr><td>Freestyle Precision Xceed&amp;nbsp;</td><td>Abbott</td><td></td><td>To measure blood glucose level during the hyperinsulinemic-euglycemic clamp</td></tr><tr><td>Insulin Novorapid</td><td>Novo Nordisk</td><td></td><td></td></tr><tr><td>Glucose monohydrate&amp;nbsp;</td><td>Merck Millipore</td><td>1083421000</td><td></td></tr><tr><td>Buffered saline solution</td><td>B. Braun</td><td>152118062</td><td></td></tr><tr><td>PE-20 medical tubing</td><td>Becton, Dickinson and Company</td><td>427405</td><td></td></tr><tr><td>Needle, 27 Gauge&amp;nbsp;</td><td>Becton-Dickinson &amp;amp; Co</td><td>305109</td><td></td></tr><tr><td>Medical tape</td><td>3M</td><td></td><td></td></tr><tr><td>Ultrasound probe holder</td><td></td><td></td><td>Built In-house</td></tr><tr><td>Cotton swabs</td><td></td><td></td><td>Multiple Equivalent</td></tr><tr><td>Creme depilator</td><td></td><td></td><td>Multiple Equivalent</td></tr><tr><td>Gel tissue adhesive</td><td>Derma+flex</td><td>GA30005-2222</td><td></td></tr><tr><td>Infusion pump</td><td>Harvard Apparatus</td><td>Harvard Apparatus PHD 2000</td><td></td></tr><tr><td>Small fine straight scissors</td><td>Fine Science Tools (FST)</td><td>14090-09</td><td></td></tr><tr><td>Needle holder</td><td>Fine Science Tools (FST)</td><td>12500-12</td><td></td></tr><tr><td>Straight forceps with fine tip</td><td>Fine Science Tools (FST)</td><td>11251-20</td><td></td></tr><tr><td>Stereomicroscope</td><td>Olympus</td><td>SZX12</td><td></td></tr><tr><td>Camera</td><td>Basler</td><td>scA1390-17gc</td><td></td></tr><tr><td>Image Grabber program</td><td>Built in-house</td><td></td><td>Image acquisition system</td></tr><tr><td>Timer</td><td>VWR</td><td>33501-418</td><td></td></tr><tr><td>Syringes, 1 mL</td><td>Fisher</td><td>14-817-25</td><td></td></tr><tr><td>Light source, fiber-optic</td><td>Schott</td><td>KL1500</td><td>Ideally has adjustable arms</td></tr><tr><td>Paraffin oil</td><td></td><td></td><td>Multiple Equivalent</td></tr><tr><td>&lt;strong&gt;Name&lt;/strong&gt;</td><td>&lt;strong&gt;Company&lt;/strong&gt;</td><td>&lt;strong&gt;Catalog Number&lt;/strong&gt;</td><td>&lt;strong&gt;Comments&lt;/strong&gt;</td></tr><tr><td>&lt;strong&gt;Microbubbles&lt;/strong&gt;</td><td></td><td></td><td></td></tr><tr><td>1,2-Distearoyl-sn-glycero-3-phosphocholine&amp;nbsp;</td><td>Avanti Polar Lipids</td><td>850365C</td><td></td></tr><tr><td>polyoxyethylene stearate&amp;nbsp;</td><td>&amp;nbsp;Sigma</td><td>p3440</td><td></td></tr><tr><td>perfluorobutane gas&amp;nbsp;</td><td>F2 Chemicals</td><td>C4F10(g)</td><td></td></tr><tr><td>Decon FS200 ultrasonic bath&amp;nbsp;</td><td>Decon Ultrasonics Ltd</td><td></td><td></td></tr><tr><td>Vialmix&amp;nbsp;</td><td>Lantheus Medical Imaging</td><td>515370-0810</td><td></td></tr><tr><td>Multisizer Coulter Counter</td><td>Beckman Coulter Inc</td><td></td><td></td></tr></tbody></table>

combined intravital microscopy and contrast-enhanced ultrasonography of the mouse hindlimb to study insulin-induced vasodilation and muscle perfusion

It has been demonstrated that insulin's vascular actions contribute to regulation of insulin sensitivity. Insulin's effects on muscle perfusion regulate postprandial delivery of nutrients and hormones to insulin-sensitive tissues. We here describe a technique for combining intravital microscopy (IVM) and contrast-enhanced ultrasonography (CEUS) of the adductor compartment of the mouse hindlimb to simultaneously visualize muscle resistance arteries and perfusion of the microcirculation in vivo. Simultaneously assessing insulin's effect at multiple levels of the vascular tree is important to study relationships between insulin's multiple vasoactive effects and muscle perfusion. Experiments in this study were performed in mice. First, the tail vein cannula is inserted for the infusion of anesthesia, vasoactive compounds and ultrasound contrast agent (lipid-encapsulated microbubbles). Second, a small incision is made in the groin area to expose the arterial tree of the adductor muscle compartment. The ultrasound probe is then positioned at the contralateral upper hindlimb to view the muscles in cross-section. To assess baseline parameters, the arterial diameter is assessed and microbubbles are subsequently infused at a constant rate to estimate muscle blood flow and microvascular blood volume (MBV). When applied before and during a hyperinsulinemic-euglycemic clamp, combined IVM and CEUS allow assessment of insulin-induced changes of arterial diameter, microvascular muscle perfusion and whole-body insulin sensitivity. Moreover, the temporal relationship between responses of the microcirculation and the resistance arteries to insulin can be quantified. It is also possible to follow-up the mice longitudinally in time, making it a valuable tool to study changes in vascular and whole-body insulin sensitivity.

Glucose infusion rate during the hyperinsulinemic-euglycemic clamp (insulin sensitivity) was 180.21 &#177; 19.81 &#181;mol/kg/min. Local application of paraffin oil on the adductor muscle compartment to stabilize the vessel did not change the average baseline diameter of the arteries (73.6 &#177; 29.0 &#181;m vs. 68.8 &#177; 17.9 &#181;m; p = 0.58) but helped reduce the variation the animals tested (Figure 4A). Insulin consistently increased the gracilis artery diameter (by 14.58 &#177; 6.2% at 60 min; N = 9) which was significantly different (p &#60;0.0001) from the diameter change caused by saline infusion (-6.3 &#177; 4.9%; N = 6). Insulin-induced vasodilation was appreciable after 10 min (10.09 &#177; 5.1%; p = 0.002) and reached approximately 95% of its maximum dilatory capacity after 30 min.
Using CEUS, insulin consistently increased muscle MBV (Figure 5A) by 33.5% (&#177; 31.04%, N =7; p = 0.0009) when compared to saline infusion (-10.63 &#177; 27.87%, N = 6) (Figure 5B). The data presented are the signal intensities of the muscle MBV divided by that in the femoral vessels. This reduces experimental variation between different measurements and between different mice (data not shown). The signal intensity in the femoral vessels corresponds linearly with the concentration of microbubbles in the circulation (Figure 3C). Correcting for the femoral vessels&#39; signal theoretically corrects for differences in concentrations of microbubbles used (Figure 3D). Data are presented in this section as mean &#177; standard deviation.
<img alt="Figure 1" src="/files/ftp_upload/54912/54912fig1.jpg" /> 
Figure 1: Surgical Exposition of the Adductor Compartment of the Hindlimb. (A) An incision is made at the groin, parallel to the direction of the inguinal ligament. (B) Gentle traction at the fat pad in the distal directions (black arrows) will present the connective tissue (*) between the fat pad and the abdominal wall. (C) The skin folds of the incision can be adjusted using the bulldog clamp to create a small cavity to hold the paraffin oil that bathes the vessels. (D) The ultrasound probe is positioned on the contralateral upper hindlimb after the prepared gracilis artery is viewed using a calibrated microscope. <a href="https://cloudflare-jove-com.remotexs.ntu.edu.sg/files/ftp_upload/54912/54912fig1large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 2" src="/files/ftp_upload/54912/54912fig2.jpg" /> 
Figure 2: Intravital Microscopy of the Mouse Hindlimb. The femoral artery (A) gives rise to the epigastric artery (B) and the gracilis artery (C) which runs over the adductor muscle group (D). The gracilis artery is used for the IVM using a calibrated microscope. <a href="https://cloudflare-jove-com.remotexs.ntu.edu.sg/files/ftp_upload/54912/54912fig2large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 3" src="/files/ftp_upload/54912/54912fig3.jpg" /> 
Figure 3: Signal Intensity of Contrast-enhanced Ultrasonography in Muscle Microvascular Blood Volume and Femoral Vessels. (A) View of the nonlinear contrast imaging mode of the digital imaging platform during microbubbles constant infusion in a male mouse upper hindlimb. Right panel: two ROIs are drawn to represent the muscle MBV and the femoral vessels. Only the superficial part of the adductor muscle compartment is included in the ROI as the signal intensity decreases with depth. Left panel: time-intensity curve from the muscle MBV ROI. Vertical lines represent the destruction of the microbubbles (MBD) with high energy waves. Immediately after the MBD, no contrast agent is present in the imaging plane which starts to fill with microbubbles gradually. After 10-15 s, the peak of the contrast enhancement has been reached. (B-D) After a steady-state signal was reached, the infusion rate of 2.5 x 109 bubbles/mL was doubled (5, 10, 20 &#181;L/min). Signal intensity from muscle MBV (B) and femoral vessels (C) paralleled the doubling of the microbubble concentration in the circulation. (D) Correcting muscle MBV for the femoral vessels signal removes the variability in signal intensity caused by different microbubble concentrations (N = 9; error-bars represent standard deviation). <a href="https://cloudflare-jove-com.remotexs.ntu.edu.sg/files/ftp_upload/54912/54912fig3large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 4" src="/files/ftp_upload/54912/54912fig4.jpg" /> 
Figure 4: Intravital Microscopy Measurements of the Gracilis Artery. (A) Paraffin oil reduces the variation of the gracilis arteries of different animals (which is 29.0 &#181;m without paraffin vs 17.9 &#181;m after applying the oil) while keeping the average baseline diameter stable (73.6 &#181;m vs. 68.8 &#181;m; p = 0.58). (B) Arterial diameters at baseline and after 60 min of insulin or saline infusions. Insulin after 60 min infusion consistently dilated the gracilis artery (p &#60;0.0001) when compared to saline infusion. (C) Insulin-induced vasodilation occurs at 10 min after the start of infusion (p = 0.002) and reaches 95% of the maximum at 30 min. Error-bars represent standard deviation; unpaired Student&#39;s T-test is used for statistics. <a href="https://cloudflare-jove-com.remotexs.ntu.edu.sg/files/ftp_upload/54912/54912fig4large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 5" src="/files/ftp_upload/54912/54912fig5.jpg" /> 
Figure 5: Microvascular Blood Volume Measurements using Contrast-enhanced Ultrasonography of the Adductor Muscle Compartment of the Mouse Hindlimb. (A) Insulin resulted in a consistent increase in MBV 30 min after the start of insulin infusion. (B) The difference between the hyperinsulinemic and the baseline measurements (MBV change) is denoted as the insulin-mediated&#160;microvascular recruitment. Insulin induced a 33.5% (&#177; 31.04%, p = 0.016; N = 7) microvascular recruitment compared to saline infusion (-10.63 &#177; 27.87%, N = 6). Error-bars represent standard deviation; unpaired Student&#39;s T-test is used for statistics. <a href="https://cloudflare-jove-com.remotexs.ntu.edu.sg/files/ftp_upload/54912/54912fig5large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>

Watch this Scientific Journal Video about Combined Intravital Microscopy and Contrast-enhanced Ultrasonography of the Mouse Hindlimb to Study Insulin-induced Vasodilation and Muscle Perfusion at JoVE.

Combined Intravital Microscopy and Contrast-enhanced Ultrasonography of the Mouse Hindlimb to Study Insulin-induced Vasodilation and Muscle Perfusion

Insulin-induced vasodilation regulates muscle perfusion and increases the microvascular surface area (microvascular recruitment) available for solute exchange between blood and tissue interstitium. Combined intravital microscopy and contrast-enhanced ultrasonography is presented to simultaneously assess insulin&#39;s action at the larger vessels and the microcirculation in vivo.

It has been demonstrated that insulin's vascular actions contribute to regulation of insulin sensitivity. Insulin's effects on muscle perfusion regulate ...

combined-intravital-microscopy-contrast-enhanced-ultrasonography

Nanyang Technological University

Research

JoVE Journal

Medicine

8.7K Views.  VU University Medical Center. Insuline-geïnduceerde vasodilatatie regelt spier perfusie en verhoogt de Microvasculaire oppervlakte (microvasculaire werving) beschikbaar voor opgeloste uitwisseling tussen bloed en weefsel interstitium. Gecombineerde intravital microscopie en contrast-enhanced Ultrasonografie is bedoeld om te beoordelen gelijktijdig insuline de actie op de grotere schepen en de microcirculatie in vivo.

Video: Combined Intravital Microscopy and Contrast-enhanced Ultrasonography of the Mouse Hindlimb to Study Insulin-induced Vasodilation and Muscle Perfusion

In vivo Micro-circulation Measurement in Skeletal Muscle by Intra-vital Microscopy

BACKGROUND: Regulatory factors and detailed physiology of in vivo microcirculation have remained not fully clarified after many different modalities of imaging had invented. While many macroscopic parameters of blood flow reflect flow velocity, changes in blood flow velocity and red blood cell (RBC) flux does not hold linear relationship in the microscopic observations. There are reports of discrepancy between RBC velocity and RBC flux, RBC flux and plasma flow volume, and of spatial and temporal heterogeneity of flow regulation in the peripheral tissues in microscopic observations, a scientific basis for the requirement of more detailed studies in microcirculatory regulation using intravital microscopy. METHODS: We modified Jeff Lichtman's method of in vivo microscopic observation of mouse sternomastoid muscles. Mice are anesthetized,
ventilated, and injected with PKH26L-fluorescently labeled RBCs for microscopic observation.RESULT &amp; CONCLUSIONS: Fluorescently labeled RBCs are detected and distinguished well by a wide-field microscope. Muscle contraction evoked by electrical stimulation induced increase in RBC flux. Quantification of other parameters including RBC velocity and capillary density were feasible. Mice tolerated well the surgery, injection of stained RBCs, microscopic observation, and electrical stimulation. No muscle or blood vessel damage was observed, suggesting that our method is relatively less invasive and suited for long-term observations.

A new versatile method for observation of microcirculation is presented. It is considered suitable for long-term observation, and for combination with pharmacophysiological or molecular biological interventions.

BACKGROUND: Regulatory factors and detailed physiology of in vivo microcirculation have remained not fully clarified after many different modalities of ...

Biology

Murine Model of Hindlimb Ischemia 

In the United States, peripheral arterial disease (PAD) affects about 10 million individuals, and is also prevalent worldwide. Medical therapies for symptomatic relief are limited. Surgical or endovascular interventions are useful for some individuals, but long-term results are often disappointing. As a result, there is a need for developing new therapies to treat PAD. The murine hindlimb ischemia preparation is a model of PAD, and is useful for testing new therapies. When compared to other models of tissue ischemia such as coronary or cerebral artery ligation, femoral artery ligation provides for a simpler model of ischemic tissue. Other advantages of this model are the ease of access to the femoral artery and low mortality rate. 
In this video, we demonstrate the methodology for the murine model of unilateral hindimb ischemia. The specific materials and procedures for creating and evaluating the model will be described, including the assessment of limb perfusion by laser Doppler imaging. This protocol can also be utilized for the transplantation and non-invasive tracking of cells, which is demonstrated by Huang et al.1.

Murine Model of Hindlimb Ischemia

The surgical procedure for induction of unilateral hindlimb ischemia is demonstrated, with confirmation of ischemia by laser Doppler perfusion imaging.

In the United States, peripheral arterial disease (PAD) affects about 10 million individuals, and is also prevalent worldwide.  Medical therapies for ...

Methods for Acute and Subacute Murine Hindlimb Ischemia

Peripheral artery disease (PAD) is a leading cause of cardiovascular morbidity and mortality in developed countries, and animal models that reliably reproduce the human disease are necessary to develop new therapies for this disease. The mouse hindlimb ischemia model has been widely used for this purpose, but the standard practice of inducing acute limb ischemia by ligation of the femoral artery can result in substantial tissue necrosis, compromising investigators&#39; ability to study the vascular and skeletal muscle tissue responses to ischemia. An alternative approach to femoral artery ligation is the induction of gradual femoral artery occlusion through the use of ameroid constrictors. When placed around the femoral artery in the same or different locations as the sites of femoral artery ligation, these devices occlude the artery over 1 - 3 days, resulting in more gradual, subacute ischemia. This results in less substantial skeletal muscle tissue necrosis, which may more closely mimic the responses seen in human PAD. Because genetic background influences outcomes in both the acute and subacute ischemia models, consideration of the mouse strain being studied is important in choosing the best model. This paper describes the proper procedure and anatomical placement of ligatures or ameroid constrictors on the mouse femoral artery to induce subacute or acute hindlimb ischemia in the mouse.

Surgical induction of hindlimb ischemia in the mouse is useful to examine angiogenesis, however this is compromised in certain inbred mouse strains that display marked ischemia-induced tissue necrosis. Methods are described to induce subacute limb ischemia using ameroid constrictors to circumvent this problem through the induction of gradual arterial occlusion.

Peripheral artery disease (PAD) is a leading cause of cardiovascular morbidity and mortality in developed countries, and animal models that reliably ...

Laser Doppler: A Tool for Measuring Pancreatic Islet Microvascular Vasomotion In Vivo

As a functional status of microcirculation, microvascular vasomotion is important for the delivery of oxygen and nutrients and the removal of carbon dioxide and waste products. The impairment of microvascular vasomotion might be a crucial step in the development of microcirculation-related diseases. In addition, the highly vascularized pancreatic islet is adapted to support endocrine function. In this respect, it seems possible to infer that the functional status of pancreatic islet microvascular vasomotion might affect pancreatic islet function. Analyzing the pathological changes of the functional status of pancreatic islet microvascular vasomotion may be a feasible strategy to determine contributions that pancreatic islet microcirculation makes to related diseases, such as diabetes mellitus, pancreatitis, etc. Therefore, this protocol describes using a laser Doppler blood flow monitor to determine the functional status of pancreatic islet microvascular vasomotion, and to establish parameters (including average blood perfusion, amplitude, frequency, and relative velocity of pancreatic islet microvascular vasomotion) for evaluation of the microcirculatory functional status. In a streptozotocin-induced diabetic mouse model, we observed an impaired functional status of pancreatic islet microvascular vasomotion. In conclusion, this approach for assessing pancreatic islet microvascular vasomotion in vivo may reveal mechanisms relating to pancreatic islet diseases.

Laser Doppler: A Tool for Measuring Pancreatic Islet Microvascular Vasomotion In Vivo

Pancreatic islet microvascular vasomotion regulates islet blood distribution and maintains the physiological function of islet &#946; cells. This protocol describes using a laser Doppler monitor to determine the functional status of pancreatic islet microvascular vasomotion in vivo and to assess the contributions of pancreatic islet microcirculation to pancreatic-related diseases.

As a functional status of microcirculation, microvascular vasomotion is important for the delivery of oxygen and nutrients and the removal of carbon ...

Quantitative Micro-CT Analysis of Aortopathy in a Mouse Model of &#946;-aminopropionitrile-induced Aortic Aneurysm and Dissection

Aortic aneurysm and dissection is associated with significant morbidity and mortality in the population and can be highly lethal. While animal models of aortic disease exist, in vivo imaging of the vasculature has been limited. In recent years, micro-computerized tomography (micro-CT) has emerged as a preferred modality for imaging both large and small vessels both in vivo and ex vivo. In conjunction with a method of vascular casting, we have successfully used micro-CT to characterize the frequency and distribution of aortic pathology in &#946;-aminopropionitrile-treated C57/Bl6 mice. Technical limitations of this method include variations in the quality of the perfusion introduced by poor animal preparation, the application of proper methodologies for vessel size quantification, and the non-survivability of this procedure. This article details a methodology for the intravascular perfusion of a lead-based radiopaque silicone rubber for the quantitative characterization of aortopathy in a mouse model of aneurysm and dissection. In addition to visualizing aortic pathology, this method may be used for examining other vascular beds in vivo or vascular beds removed post-mortem.

This article describes a detailed methodology of using a radiopaque lead-based silicone rubber to perfuse the murine vasculature for aortic diameter quantification in a mouse model of aortic aneurysm and dissection.

Aortic aneurysm and dissection is associated with significant morbidity and mortality in the population and can be highly lethal. While animal models of ...

Dynamic Measurement and Imaging of Capillaries, Arterioles, and Pericytes in Mouse Heart

Coronary arterial tone along with the opening or closing of the capillaries largely determine the blood flow to cardiomyocytes at constant perfusion pressure. However, it is difficult to monitor the dynamic changes of the coronary arterioles and the capillaries in the whole heart, primarily due to its motion and non-stop beating. Here we describe a method that enables monitoring of arterial perfusion rate, pressure and the diameter changes of the arterioles and capillaries in mouse right ventricular papillary muscles. The mouse septal artery is cannulated and perfused at a constant flow or pressure with the other dynamically measured. After perfusion with a fluorescently labeled lectin (e.g., Alexa Fluor-488 or -633 labeled Wheat-Germ Agglutinin, WGA), the arterioles and capillaries (and other vessels) in right ventricle papillary muscle and septum could be readily imaged. The vessel-diameter changes could then be measured in the presence or absence of heart contractions. When genetically encoded fluorescent proteins were expressed, specific features could be monitored. For examples, pericytes were visualized in mouse hearts that expressed NG2-DsRed. This method has provided a useful platform to study the physiological functions of capillary pericytes in heart. It is also suitable for studying the effect of reagents on the blood flow in heart by measuring the vascular/capillary diameter and the arterial luminal pressure simultaneously. This preparation, combined with a state-of-the-art optic imaging system, allows one to study the blood flow and its control at cellular and molecular level in the heart under near-physiological conditions.

Presented here is a protocol to study the coronary microcirculation in living murine heart tissue by ex vivo monitoring of the arterial perfusion pressure and flow that maintains the pressure, as well as vascular tree components including the capillary beds and pericytes, as the septal artery is cannulated and pressurized.

Coronary arterial tone along with the opening or closing of the capillaries largely determine the blood flow to cardiomyocytes at constant perfusion ...

Laser Doppler Perfusion Imaging in the Mouse Hindlimb

Blood flow recovery is a critical outcome measure after experimental hindlimb ischemia or ischemia-reperfusion. Laser Doppler perfusion imaging (LDPI) is a common, noninvasive, repeatable method for assessing blood flow recovery. The technique calculates overall blood flow in the sampled tissue from the Doppler shift in frequency caused when a laser hits moving red blood cells. Measurements are expressed in arbitrary perfusion units, so the contralateral non-intervened upon leg is usually used to help control measurements. Measurement depth is in the range of 0.3-1 mm; for hindlimb ischemia, this means that dermal perfusion is assessed. Dermal perfusion is dependent on several factors&#8212;most importantly skin temperature and anesthetic agent, which must be carefully controlled to result in reliable readings. Furthermore, hair and skin pigmentation can alter the ability of the laser to either reach or penetrate to the dermis. This article demonstrates the technique of LDPI in the mouse hindlimb.

Here, we present a protocol that demonstrates the technique and necessary controls for Laser Doppler perfusion imaging to measure blood flow in the mouse hindlimb.

Blood flow recovery is a critical outcome measure after experimental hindlimb ischemia or ischemia-reperfusion. Laser Doppler perfusion imaging (LDPI) is ...

Stabilized Longitudinal In Vivo Cellular-Level Visualization of the Pancreas in a Murine Model with a Pancreatic Intravital Imaging Window

Direct in vivo cellular-resolution imaging of the pancreas in a live small animal model has been technically challenging. A recent intravital imaging study, with an abdominal imaging window, enabled visualization of the cellular dynamics in abdominal organs in vivo. However, due to the soft sheet-like architecture of the mouse pancreas that can be easily influenced by physiologic movement (e.g., peristalsis and respiration), it was difficult to perform stabilized longitudinal in vivo imaging over several weeks at the cellular level to identify, track, and quantify islets or cancer cells in the mouse pancreas. Herein, we describe a method for implanting a novel supporting base, an integrated pancreatic intravital imaging window, that can spatially separate the pancreas from the bowel for longitudinal time-lapse intravital imaging of the pancreas microstructure. Longitudinal in vivo imaging with the imaging window enables stable visualization, allowing for the tracking of islets over a period of 3 weeks and high-resolution three-dimensional imaging of the microstructure, as evidenced here in an orthotopic pancreatic cancer model. With our method, further intravital imaging studies can elucidate the pathophysiology of various diseases involving the pancreas at the cellular level.

Stabilized Longitudinal In Vivo Cellular-Level Visualization of the Pancreas in a Murine Model with a Pancreatic Intravital Imaging Window

In vivo high-resolution imaging of the pancreas was facilitated with the pancreatic intravital imaging window.

Direct in vivo cellular-resolution imaging of the pancreas in a live small animal model has been technically challenging. A recent intravital imaging ...

Multiphoton Intravital Imaging for Monitoring Leukocyte Recruitment during Arteriogenesis in a Murine Hindlimb Model

Arteriogenesis strongly depends on leukocyte and platelet recruitment to the perivascular space of growing collateral vessels. The standard approach for analyzing collateral arteries and leukocytes in arteriogenesis is ex vivo (immuno-) histological methodology. However, this technique does not allow the measurement of dynamic processes such as blood flow, shear stress, cell-cell interactions, and particle velocity. This paper presents a protocol to monitor in vivo processes in growing collateral arteries during arteriogenesis utilizing intravital imaging. The method described here is a reliable tool for dynamics measurement and offers a high-contrast analysis with minimal photo-cytotoxicity, provided by multiphoton excitation microscopy. Prior to analyzing growing collateral arteries, arteriogenesis was induced in the adductor muscle of mice by unilateral ligation of the femoral artery.
After the ligation, the preexisting collateral arteries started to grow due to increased shear stress. Twenty-four hours after surgery, the skin and subcutaneous fat above the collateral arteries were removed, constructing a pocket for further analyses. To visualize blood flow and immune cells during in vivo imaging, CD41-fluorescein isothiocyanate (FITC) (platelets) and CD45-phycoerythrin (PE) (leukocytes) antibodies were injected intravenously (i.v.) via a catheter placed in the tail vein of a mouse. This article introduces intravital multiphoton imaging as an alternative or in vivo complementation to the commonly used static ex vivo (immuno-) histological analyses to study processes relevant for arteriogenesis. In summary, this paper describes a novel and dynamic in vivo method to investigate immune cell trafficking, blood flow, and shear stress in a hindlimb model of arteriogenesis, which enhances evaluation possibilities notably.

The recruitment of leukocytes and platelets constitutes an essential component necessary for the effective growth of collateral arteries during arteriogenesis. Multiphoton microscopy is an efficient tool for tracking cell dynamics with high spatio-temporal resolution in vivo and less photo-toxicity to study leukocyte recruitment and extravasation during arteriogenesis.

Arteriogenesis strongly depends on leukocyte and platelet recruitment to the perivascular space of growing collateral vessels. The standard approach for ...

High-Resolution Three-Dimensional Imaging of the Footpad Vasculature in a Murine Hindlimb Gangrene Model

Peripheral arterial disease (PAD) is a significant cause of morbidity resulting from chronic exposure to atherosclerotic risk factors. Patients suffering from its most severe form, chronic limb-threatening ischemia (CLTI), face substantial impairments to daily living, including chronic pain, limited walking distance without pain, and nonhealing wounds. Preclinical models have been developed in various animals to study PAD, but mouse hindlimb ischemia remains the most widely used. There can be significant variation in response to ischemic insult in these models depending on the mouse strain used and the site, number, and means of arterial disruption. This protocol describes a unique method combining femoral artery and vein electrocoagulation with the administration of a nitric oxide synthase (NOS) inhibitor to reliably induce footpad gangrene in Friend Virus B (FVB) mice that resembles the tissue loss of CLTI. While traditional means of assessing reperfusion such as laser Doppler perfusion imaging (LDPI) are still recommended, intracardiac perfusion of the lipophilic dye 1,1'-dioctadecyl-3,3,3',3'-tetramethylindocarbocyanine perchlorate (DiI) is used to label the vasculature. Subsequent whole-mount confocal laser scanning microscopy allows for high-resolution, three-dimensional (3D) reconstruction of footpad vascular networks that complements traditional means of assessing reperfusion in hindlimb ischemia models.

The present protocol describes a unique, clinically relevant model of peripheral arterial disease that combines femoral artery and vein electrocoagulation with the administration of a nitric oxide synthase inhibitor to induce hindlimb gangrene in FVB mice. Intracardiac DiI perfusion is then used for high-resolution, three-dimensional imaging of the footpad vasculature.

Peripheral arterial disease (PAD) is a significant cause of morbidity resulting from chronic exposure to atherosclerotic risk factors. Patients suffering ...

Combined Intravital Microscopy and Contrast-enhanced Ultrasonography of the Mouse Hindlimb to Study Insulin-induced Vasodilation and Muscle Perfusion

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