Source: Kay Stewart, RVT, RLATG, CMAR; Valerie A. Schroeder, RVT, RLATG. University of Notre Dame, IN
In 1959 The 3 R's were introduced by W.M.S. Russell and R.L. Burch in their book The Principles of Humane Experimental Technique. The 3 R's are replacement, reduction, and refinement of the use of animals in research.1 The use of cell lines and tissue cultures that originated from research animals is a replacement technique, as it allows for many experiments to be conducted in vitro. Harvesting tissues and organs for use in cell and tissue cultures requires aseptic technique to avoid contamination of the tissues. Sterile harvest is also necessary for protein and RNA analysis and metabolic profiling of tissues. This manuscript will discuss the process of sterile organ harvest in rats and mice.
Aseptic technique must be followed to ensure the sterility of the tissues. The harvest is performed in a laminar flow hood that has been disinfected with alcohol. All materials used must be sterilized. The technician performing the harvest must don personal protective equipment, including a mask, bouffant, sterile surgical gown, and sterile surgical gloves. The gown must cover the wrists to prevent the shedding of skin cells into the opened body cavity, petri dishes, or sterile medium. To maintain sterility of the technician, this procedure requires that a second, nonsterile technician assist the sterile technician with the euthanasia of the animals.
In experiments that require the metabolic profiles of tissues, the method of tissue harvest has a great impact on the quality of the data collected.2 Both the euthanasia procedure and the length of time the harvest takes can affect the integrity of tissues. Hypoxia, a consequence of euthanasia with carbon dioxide, has been shown to have a profound effect on the metabolites in tissues. Hemorrhaging of the vessels in lung tissue is also caused by the use of carbon dioxide for euthanasia. The order of tissue removal when sequential dissection of targeted tissues is performed can cause metabolic changes, as the tissues begin to age or decay during the harvest.
While most sterile harvests target a single organ, there may be times that more than one organ is needed. During sequential dissection, the tissues required will dictate the order in which they should be removed.2 Tissues that rapidly degrade must be harvested as quickly as possible following euthanasia. To maintain sterility of the instruments, organs harvested from the abdominal cavity are removed in the following order: spleen, liver, kidney, adrenal glands, ovary or testes, accessory sex organs (prostate, seminal vesicles, uterus, fallopian tubes), pancreatic tissue, lymph nodes, urinary bladder, and intestinal tract (stomach, small and large intestine). The order of the organ harvest from the thoracic cavity is to first remove the heart and lungs followed by the collection of thymus, lymph nodes, and esophagus.3 New gloves are required for each mouse.
Some of the sterile harvested organs may need to be preserved. Preservation of the tissues is accomplished by flash freezing with liquid nitrogen (LN2) or with a combination of LN2 and 2-methylbutane. For LN2 alone, the tissues are rinsed in sterile saline, blotted on a sterile absorbent cloth to deplete excess moisture, placed in sterile aluminum foil squares, and immediately submerged into the LN2.2 For immunological specimens, 2-methylbutane is added. The tissue is actually submerged into the 2-methylbutane that has been cooled down by the LN2. When the tissues have turned white, they are removed from the 2-methylbutane, placed in sterile packs, and then placed directly into the LN2.
1. Preparation
2. Harvesting tissues
Although many of the procedures for sterile organ harvest are similar to a standard necropsy, the use of sterile technique is imperative for tissues to be of value for experimental procedures, which include harvesting cells from the excised tissues. Profiling or collecting RNA from tissues can be compromised if sterility is not maintained.
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