Contemporary topics in laboratory animal science最新文献

To remain at the forefront of scientific discovery, investigators continually are challenged to apply new approaches, instruments, and models to their work. Research institutions work to foster the exchange of ideas and resources, but this objective becomes more difficult to meet as the organization's size and complexity increase. To facilitate communication among researchers that use mice in their work and to provide increased opportunities for resource sharing, an electronic discussion group was formed at The Johns Hopkins University. The discussion group (jhu-mousers) is restricted to individuals within the institution's three campuses, and its 145 subscribers comprise faculty (including veterinarians), postdoctoral fellows, graduate students, and technicians. During its beginning 2 1/2-year period, jhu-mousers has received 207 postings that include seminar announcements; resource information; requests for mice, equipment, biological reagents, and technical assistance; and responses to these requests. The value of the electronic mailing list is evidenced by the fact that 70% of requests for resources or technical help have received at least one response, and this figure is likely to be underestimated because off-line responses are not included. Because the mailing list provides opportunities for tissue sharing and is conducive to refining experimental procedures used in mice, its application promotes the use of alternatives in animal research. To promote and assist the development of animal-user discussion groups at other institutions, the administration, applications, and benefits of an electronic mailing list for mouse users are discussed here.

Monodelphis domestica, a South American marsupial, has been developed as a laboratory animal model for allogeneic and xenogeneic cancer research by taking advantage of its underdeveloped immune system in the early days of life. The limited immunological capability during this period provides an opportunity to induce tolerance to grafted tumor tissue in juvenile and adult opossums. In this study, we injected multiple doses of mouse B16 melanoma cells into opossums at different developmental ages (i.e., suckling young, juveniles, and adults) to determine whether immunotolerance could develop as a result of repeated "desensitizing" injections. We found that establishment and growth of xenografted mouse melanoma cells could be established after full immune capability of the animals had been achieved. The tumors thus produced could sustain their growth for as long as 6 weeks before beginning to regress. Our results highlight the potential of the laboratory opossum as a natural mammalian model to study host immunotolerance to xenografted tumor cells.

The purpose of this experiment was to assess the practicality, ease, and reliability of using tympanic, transponder, and noncontact infrared laser thermometry versus rectal thermometry in strain 13 guinea pigs. Body temperatures were measured by all four methods within each animal over 10 min, and three sets of measurements were taken over 2 days. Each method was compared for agreement over time and agreement with the rectal temperature of each animal. Over time the transponder temperatures were the most reliable and had the closest agreement with the rectal temperatures. There was an overall difference in mean temperatures among methods but not between times, indicating that the guinea pigs had stable body temperatures over different time periods. Although the mean temperatures from the transponder and tympanic thermometers were not significantly different from the rectal temperatures, only the transponder method was in close agreement with the rectal method. The tympanic and noncontact infrared laser methods had poor agreement with the rectal method. These study results suggest that transponder thermometry is an easy and accurate alternative to rectal thermometry in strain 13 guinea pigs.

We conducted this study to determine whether heart rate, respiratory rate, and recovery time differed significantly between rats receiving target-controlled infusion (TCI) and those under volatile inhalant anesthesia. TCI rats received intravenous propofol at an average effect site concentration of 11.3 microg/ml or propofol plus ketamine (5 mg/ml of propofol) at an average effect site concentration of 8.7 microg/ml. Inhalant anesthesia rats received isoflurane (average, 1.8%) delivered in medical-grade air. We used a tail-clamp response test to determine when a surgical plane of anesthesia was attained. Anesthesia was continued for 1 h from the first negative tail-clamp test. During this time the test was repeated every 10 min to confirm that a surgical plane of anesthesia was being maintained. Anesthesia then was discontinued, and the animals were monitored continuously until they recovered. Average heart rate was higher for rats during anesthesia with isoflurane compared with TCI propofol-ketamine (P =0.0053). Average respiratory rate was higher for TCI regimens compared with isoflurane anesthesia, with male rats having consistently faster respiratory rates than females (P <0.001). Recovery time was longer for both TCI regimens compared with isoflurane (P <0.001). Once venous access was accomplished, TCI anesthesia with propofol or propofol combined with a low dose of ketamine was comparable to an isoflurane inhalant regimen in ease of administration and control of the anesthetic event when used in rats for procedures of 1-h duration. Respiratory rate was increased and recovery time was longer for rats receiving the TCI regimens.

After a 4-year-old female laboratory cynomolgus monkey manifested neurological abnormalities, including tetanic spasm, after intramuscular injection of 20 mg/kg ketamine, we administered 2 mg/kg xylazine in an attempt to control the seizure. However, the animal continued to display opisthotonus, nystagmus, and symptomatic epilepsia. Analysis of blood chemistry revealed a dramatically increased creatine phosphokinase level. Abnormal histopathological findings included acute neuronal necrosis or glial reaction or both in the cerebral cortex, nucleus lentiformis, hippocampus, cerebellar cortex and nucleus, and medulla oblongata; severe myocardial hemorrhagic necrosis; and hepatic subcapsular hematoma. Although the mechanism of this neuronal damage has not been clarified, it may be attributable to an ischemic condition in the brain, probably due to temporal cardiac arrest or hemorrhagic change in the liver and heart, with subsequent decreased blood pressure, after ketamine and/or xylazine treatment. Because both drugs often are used as general anesthetics in veterinary medicine, attention should be paid to this rare case with neural damage.

The tropical rat mite, Ornithonyssus bacoti, was identified in a colony of mutagenized and transgenic mice at a large academic institution. O. bacoti is an obligate, blood-feeding ectoparasite with an extensive host range. Although the source of the infestation was likely feral rodents, none were found in the room housing infested mice. We hypothesize that construction on the floor above the vivarium and compromised ceiling integrity within the animal room provided for vermin entry and subsequent O. bacoti infestation. O. bacoti infestation was eliminated by environmental decontamination with synthetic pyrethroids and weekly application of 7.4% permethrin-impregnated cotton balls to mouse caging for five consecutive weeks. Visual examination of the macroenvironment, microenvironment, and colony for 38 days confirmed the efficacy of treatment. We noted no treatment-related toxicities or effects on colony production.

Social housing has been shown to contribute to the psychological well-being and physical health of captive primates, and this factor has led to United States Department of Agriculture guidelines requiring facilities to address the social needs of primate species known to live socially in nature as long as doing so does not endanger the animals or interfere with research goals. Although pair-housing is the best way to provide social enrichment, many researchers and facilities are hesitant to implement it, particularly in biomedical research contexts where implanted devices or behavioral performance might be compromised. In order to study the effects of pair-housing on biomedical implants and study participation, we collected data from a group of isosexually pair-housed male macaques (adult and subadult) with 1) cranial and eye implants and 2) controlled access to water as means of motivating subjects to participate in psychophysical studies. Implants, study participation, and weight gain were not adversely affected by pair-housing. Our results support the use of pair-housing as social enrichment for macaques with biomedical implants and controlled access to water.

Skin lesions, consisting of nonspecific bites with intense pruritus and excoriation of the skin, were found on personnel working in an animal colony primarily housing mice. The tropical rat mite, Ornithonyssus bacoti, was diagnosed from mites trapped on insect-monitoring sticky traps and collected from mouse cages in the colony. Because these mites do not live on mice but only come to feed when the animals are in their nest, an initial attempt was made to eliminate the mites with a thorough cleaning of the facility. Clidox foam was applied to the entire room with a foaming machine. Then the mice were transferred into the sanitized cages in the cleaned room. The numbers of mites were reduced to the point that they were no longer noticed in the colony, but the mites returned within 2 weeks. The mites were successfully eliminated with the use of permethrin-impregnated cotton balls in the mouse cages for 8 weeks and treatment of the premises. Treatment of the premises included spraying floors and walls of all rooms housing mice and adjacent hallways in the colony with pyrethrin spray by a commercial pest control company. To prevent one room of rabbits from maintaining the infestation, they were treated weekly with an organic pyrethrin dust. Insect sticky traps have remained negative for mites for more than 3 years after treatment.

Study of the genetics of hypertension has been facilitated greatly by the use of mice with modified genes that affect blood pressure. A current successful method for measuring blood pressure in mice relies on detection of light passing through the tail to determine the pressure in a tail-cuff necessary to stop pulsed flow. Success in obtaining reliable blood pressure measurements in light-tailed strains of mice (e.g., C57BL/6J) has been excellent. However, in our and others' experience, mice having highly pigmented tails (e.g., 129S6/SvEvTac) have yielded less consistent measurements. We report here that simple modifications to the channel containing the pulse detection sensor can greatly improve the pulse detection of dark-tailed mice. The first modification--lining the sensor channel with four layers of clear plastic wrap--increased the frequency of successful blood pressure measurements of 129S6/SvEvTac mice twofold and reduced variability by one-third. The second modification--lining the sides of the channel with reflective foil--also improved the success rate with dark-tailed mice. Mean blood pressures were unaffected by these modifications, which enhance detection of the pulse wave and likely will be helpful in diverse applications in which blood pressure is measured in rodent strains with pigmented tails.

C-reactive protein (CRP) is used widely as an indicator of infections and recovery from infections in human medicine. It is an acute-phase serum protein, and its concentration increases in response to infection, trauma, and inflammation. In efficacy and safety studies involving chimpanzees (Pan troglodytes) as an animal model to evaluate therapeutic drugs targeting the human population, CRP may be used as a diagnostic tool in assessing animal health. Establishing normal values in healthy populations of chimpanzees is crucial to interpreting changes in CRP serum levels and how they relate to drug safety and animal health.