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1.
Adv Physiol Educ ; 44(2): 163-168, 2020 Jun 01.
Article in English | MEDLINE | ID: mdl-32167832

ABSTRACT

Blood flow through the cardiovascular system is governed by the same physical rules that govern the flow of water through domestic plumbing. Using this analogy in a teaching laboratory, a model of the cardiovascular system constructed of pumps and pipes was used to demonstrate the basic interactions of pressure, flow, and resistance in a regulated system, with student volunteers providing the operational actions and regulatory components. The model was used to validate predictions and explore solutions prompted by student discussion. This interactive teaching laboratory provides an engaging experiential exercise that demonstrates regulation of flow and pressure in an intact cardiovascular system with apposite changes in heart rate and resistance. In addition, the system provides strong clinical correlates and illustrates how that regulated system responds to challenges such as heart failure, inappropriate vasodilation, and hemorrhage. The results demonstrate that, with limited practice, the instructor can effectively guide the students to reliably reproduce physiologically appropriate results.


Subject(s)
Cardiovascular Physiological Phenomena , Laboratory Animal Science/education , Laboratory Animal Science/methods , Physiology/education , Problem-Based Learning/methods , Schools, Veterinary , Cardiovascular System , Exercise/physiology , Heart Rate/physiology , Hemodynamics/physiology , Humans
2.
J Exp Biol ; 222(Pt 9)2019 05 08.
Article in English | MEDLINE | ID: mdl-31015286

ABSTRACT

Bees are in decline globally as a result of multiple stressors including pests, pathogens and contaminants. The management of bees in enclosures can identify causes of decline under standardized conditions but the logistics of conducting effect studies in typical systems used across several colonies is complex and costly. This study details a practicable, new and economical cage system that effectively houses live honey bee colonies to investigate the impact of physical conditions, biological factors and environmental contaminants on honey bee health. The method has broad application for a range of effect studies concerning honey bee development, physiology, survival and population dynamics because it enables entire colonies, as opposed to individual workers, to be managed well in captivity.


Subject(s)
Beekeeping/methods , Bees , Laboratory Animal Science/methods , Animals , Beekeeping/economics , Laboratory Animal Science/economics
4.
J Am Assoc Lab Anim Sci ; 63(3): 232-237, 2024 May 01.
Article in English | MEDLINE | ID: mdl-38503489

ABSTRACT

The ability to apply findings from animal studies efficiently and effectively is predicated on an understanding of biology and pathobiology, how that biology relates to the human systems being modeled, and how the studies are conducted and reported. This overview discusses various factors in research within the animal environment (referred to as extrinsic factors) that the NIH now expects to be documented to foster replicability in science and expand interpretations of study outcomes. Specifically, an important extrinsic factor in research with animals is that of individual personnel who perform handling practices, participate in research interactions, and share an overall presence in the housing facility with animals, all of which can confound reproducibility efforts in biomedical science. An improved understanding of the influences and behaviors of animal research personnel on animal responses is critical with regard to research results and the interpretation of data collected from animal models of biomedical disease.


Subject(s)
Animals, Laboratory , Animals , Reproducibility of Results , United States , Housing, Animal/standards , Animal Welfare/standards , National Institutes of Health (U.S.) , Laboratory Animal Science/standards , Laboratory Animal Science/methods , Documentation/standards , Animal Husbandry/methods , Animal Husbandry/standards
5.
Mamm Genome ; 24(3-4): 89-94, 2013 Apr.
Article in English | MEDLINE | ID: mdl-23314661

ABSTRACT

Currently, there is the potential to generate over 200,000 mutant mouse strains between existing mouse strains (over 24,000) and genetically modified mouse embryonic stem cells (over 209,000) that have been entered into the International Mouse Strain Resource Center (IMSR) from laboratories and repositories all over the world. The number of rat strains is also increasing exponentially. These mouse and rat mutants are a tremendous genetic resource; however, the awareness of their genetic integrity such as genetic background and genotyping of these models is not always carefully monitored. In this review, we make a case for the International Council for Laboratory Animal Science (ICLAS), which is interested in promoting and helping academic institutions develop a genetic monitoring program to bring a level of genetic quality assurance into the scientific interchange and use of mouse and rat genetically mutant models.


Subject(s)
Biomedical Research/methods , Laboratory Animal Science/methods , Mice, Inbred Strains/genetics , Rats, Inbred Strains/genetics , Animals , Breeding/methods , Genotype , Mice , Mutation , Quality Control , Rats
6.
J Exp Zool B Mol Dev Evol ; 320(8): 538-47, 2013 Dec.
Article in English | MEDLINE | ID: mdl-24006276

ABSTRACT

Despite advances in the study on animal evolution in the last two decades, paucity of experimental data on cephalochordates comparable to those on the other chordates hinders an integrative understanding of chordate evolutionary history. To obtain lancelet data under well-controlled experiments, laboratory cultures of lancelets have been performed at several institutions. In a mass culture started in 2005, we have obtained up to three consecutive generations of Branchiostoma japonicum. Using sand substratum, survival rates of laboratory lancelets until maturation have improved to greater than 30%, much higher than compared to previously, and for adults the annual average survival rate was 82.3%. The high survival rate allows maintaining animals at least 6 years and potentially longer. Water temperatures lower than 23°C obviously reduced the frequency of spawning even after the onset of spawning period, and 1-2 days after changing the temperature at 25°C animals became spawned well. We also observed obvious sex reversal from male to female in individuals that had been cultured for 3 years or more. Our continuous culture has provided sufficient materials for vital experiments on early development and for studying metamorphosis, as well as for the conservation of wild populations. The subculture of successive laboratory generations will provide a valuable resource for genetic studies.


Subject(s)
Laboratory Animal Science/methods , Lancelets/physiology , Reproduction/physiology , Animals , Aquaculture , Female , Lancelets/genetics , Lancelets/growth & development , Loss of Heterozygosity , Male , Phylogeny , Seawater , Sex Determination Processes , Temperature
7.
J Reprod Dev ; 58(4): 501-4, 2012.
Article in English | MEDLINE | ID: mdl-22452831

ABSTRACT

In rats, artificial insemination (AI) is surgically performed as a general tool to obtain offspring using cryopreserved spermatozoa. Nonsurgical AI is a more desirable technology because it does not require any surgical procedures. However, there has never been a successful nonsurgical AI since frozen-thawed rat spermatozoa show low motility. We show here for the first time successful nonsurgical AI in rats using oxytocin treatment. Intraperitoneal injection of oxytocin (1/800 IU) immediately before nonsurgical AI significantly increased the number of sperm collected from the oviducts compared with that without oxytocin treatment. Therefore, to obtain pups, oxytocin was intraperitoneally injected into females mated with vasectomized males, and the rats were then used for nonsurgical AI. Seven of the 12 oxytocin-treated rats became pregnant after nonsurgical AI, and 37 pups were obtained. Only one rat (1/13) without oxytocin treatment was pregnant after nonsurgical AI, and only 1 pup was delivered. These results show success for the first time in obtaining offspring using frozen-thawed rat spermatozoa via nonsurgical AI. Our results also suggest the possibility that oxytocin treatment is effective for improvement of nonsurgical AI even in other species.


Subject(s)
Cryopreservation/veterinary , Fertility Agents, Female/pharmacology , Insemination, Artificial/veterinary , Laboratory Animal Science/methods , Oxytocin/pharmacology , Semen Preservation/veterinary , Animals , Female , Fertility Agents, Female/administration & dosage , Fertility Agents, Female/adverse effects , Fetal Development/drug effects , Injections, Intraperitoneal/veterinary , Insemination, Artificial/methods , Litter Size/drug effects , Male , Oxytocin/administration & dosage , Oxytocin/adverse effects , Pregnancy , Pregnancy Rate , Rats , Rats, Wistar , Semen Preservation/adverse effects , Sperm Transport/drug effects
8.
Am J Primatol ; 74(8): 712-20, 2012 Aug.
Article in English | MEDLINE | ID: mdl-22553135

ABSTRACT

Nonhuman primates in research environments experience regular stressors that have the potential to alter physiology and brain function, which in turn can confound some types of research studies. Operant conditioning techniques such as positive reinforcement training (PRT), which teaches animals to voluntarily perform desired behaviors, can be applied to improve behavior and reactivity. PRT has been used to train rhesus macaques, marmosets, and several other nonhuman primate species. To our knowledge, the method has yet to be used to train squirrel monkeys to perform complex tasks. Accordingly, we sought to establish whether PRT, utilizing a hand-box clicker (which emits a click sound that acts as the conditioned reinforcer), could be used to train adult male squirrel monkeys (Saimiri boliviensis, N = 14). We developed and implemented a training regimen to elicit voluntary participation in routine husbandry, animal transport, and injection procedures. Our secondary goal was to quantify the training time needed to achieve positive results. Squirrel monkeys readily learned the connection between the conditioned reinforcer (the clicker) and the positive reinforcer (food). They rapidly developed proficiency on four tasks of increasing difficulty: target touching, hand sitting, restraint training, and injection training. All subjects mastered target touching behavior within 2 weeks. Ten of 14 subjects (71%) mastered all tasks in 59.2 ± 2.6 days (range: 50-70 days). In trained subjects, it now takes about 1.25 min per monkey to weigh and administer an intramuscular injection, one-third of the time it took before training. From these data, we conclude that clicker box PRT can be successfully learned by a majority of squirrel monkeys within 2 months and that trained subjects can be managed more efficiently. These findings warrant future studies to determine whether PRT may be useful in reducing stress-induced experimental confounds in studies involving squirrel monkeys.


Subject(s)
Conditioning, Psychological , Reinforcement, Psychology , Saimiri/psychology , Animals , Behavior, Animal , Laboratory Animal Science/methods , Male
9.
J Exp Zool B Mol Dev Evol ; 316(4): 263-75, 2011 Jun 15.
Article in English | MEDLINE | ID: mdl-21271675

ABSTRACT

Owing to its phylogenetic position at the base of the chordates, the cephalochordate amphioxus is an emerging model system carrying immense significance for understanding the evolution of vertebrate development. One important shortcoming of amphioxus as a model organism has been the unavailability of animal husbandry protocols to maintain amphioxus adults away from the field. Here, we present the first report of successful maintenance and spawning of Branchiostoma lanceolatum adults in a facility run on artificial seawater. B. lanceolatum has been chosen for this study because it is the only amphioxus species that can be induced to spawn. We provide a step-by-step guide for the assembly of such a facility and discuss the day-to-day operations required for successful animal husbandry of B. lanceolatum adults. This work also includes a detailed description of the B. lanceolatum spawning behavior in captivity. Our analysis shows that the induced spawning efficiency is not sex biased, but increases as the natural spawning season progresses. We find that a minor fraction of the animals undergo phases of spontaneous spawning in the tanks and that this behavior is not affected by the treatment used to induce spawning. Moreover, the induced spawning efficiency is not discernibly correlated with spontaneous spawning in the facility. Last, we describe a protocol for long-term cryopreservation of B. lanceolatum sperm. Taken together, this work represents an important step toward further establishing amphioxus as a laboratory animal making it more amenable to experimental research, and hence assists the coming of age of this emerging model.


Subject(s)
Animal Husbandry/methods , Chordata, Nonvertebrate/physiology , Environment, Controlled , Laboratory Animal Science/methods , Sexual Behavior, Animal/physiology , Spermatozoa/cytology , Animals , Cryopreservation/methods , Housing, Animal , Male , Seawater
10.
Transgenic Res ; 20(6): 1245-52, 2011 Dec.
Article in English | MEDLINE | ID: mdl-21359657

ABSTRACT

In vitro fertilization (IVF) is a valuable technique for the propagation of experimental animals. IVF has typically been used in mice to rapidly expand breeding colonies and create large numbers of embryos. However, applications of IVF in rat breeding experiments have stalled due to the inconvenient laboratory work schedules imposed by current IVF protocols for this species. Here, we developed a new rat IVF protocol that consists of experimental steps performed during common laboratory working hours. Our protocol can be completed within 12 h by shortening the period of sperm capacitation from 5 to 1 h and the fertilization time from 10 to 8 h in human tubal fluid (HTF) medium. This new protocol generated an excellent birth rate and was applicable not only to closed colony rat strains, such as Wistar, Long-Evans, and Sprague-Dawley (SD), but also to the inbred Lewis strain. Moreover, Wistar and Long-Evans embryos prepared by this protocol were successfully frozen by vitrification and later successfully thawed and resuscitated. This protocol is practical and can be easily adopted by laboratory workers.


Subject(s)
Embryo, Mammalian/physiology , Fertilization in Vitro/methods , Laboratory Animal Science/methods , Animals , Breeding/methods , Cryopreservation/methods , Culture Media/chemistry , Fallopian Tubes/physiology , Female , Male , Oocytes/physiology , Rats , Rats, Inbred Lew , Rats, Long-Evans , Rats, Sprague-Dawley , Rats, Wistar , Resuscitation/methods , Species Specificity , Spermatozoa/physiology , Time Factors , Vitrification
11.
Bull Entomol Res ; 101(3): 259-69, 2011 Jun.
Article in English | MEDLINE | ID: mdl-21208505

ABSTRACT

Domesticating anopheline species from wild isolates provides an important laboratory tool but requires detailed knowledge of their natural biology and ecology, especially the natural breeding habitats of immature stages. The aim of this study was to determine the optimal values of some parameters of Anopheles gambiae larval development, so as to design a standard rearing protocol of highland isolates, which would ensure: the biggest fourth instars, the highest pupae productivity, the shortest duration of the larval stage and the best synchronization of pupation. The density of larvae, the size of breeding water and the quantity of food supplied were tested for their effect on larval growth. Moreover, three cheap foodstuffs were selected and tested for their capability to improve the breeding yield versus TetraMin® as the standard control. The larval density was a very sensitive parameter. Its optimal value, which was found to be ≈1 cm-2 surface area, yielded a daily pupation peak of 38.7% on day 8 post-oviposition, and a global pupae productivity of 78.7% over a duration range of three days. Anopheles gambiae's larval growth, survival and developmental synchronization were density-dependent, and this species responded to overcrowding by producing smaller fourth instars and fewer pupae, over elongated immature lifetime and duration range of pupae occurrence, as a consequence of intraspecific competition. While shallow breeding waters (<3 cm) produced a higher number of pupae than deeper ones, no effect of the breeding habitat's absolute surface area on larval development was observed. Increasing the daily food supply improved the pupae productivity but also boosted the water pollution level (which was assessed by the biological oxygen demand (BOD) and the chemical oxygen demand (COD)) up to a limit depending on the food quality, above which a rapid increase in larval mortality was recorded. The food quality that could substitute the manufactured baby fish food was obtained with weighed mixture of 1 wheat+1 shrimp+2 fish. On establishing an anopheline mosquito colony in the laboratory, special care should be taken to design and maintain the appropriate optimal values of larval density, water depth, daily diet quantity and nutritional quality.


Subject(s)
Animals, Laboratory/growth & development , Anopheles/growth & development , Breeding/methods , Laboratory Animal Science/methods , Animals , Biological Oxygen Demand Analysis , Fertility/physiology , Fresh Water/chemistry , Larva/growth & development , Population Density , Water Pollution/analysis
12.
Lab Anim ; 55(1): 76-80, 2021 Feb.
Article in English | MEDLINE | ID: mdl-32883167

ABSTRACT

Drug administration to experimental rodents is often invasive and stressful, thus reducing animal welfare and potentially confounding experimental results. Methods of oral drug delivery in which rodents cooperate voluntarily minimize stress, pain and morbidity. We herein describe a method for oral administration through voluntary intake of strawberry jam, developed for C57BL/6J mice. During a 3-day habituation period, animals were placed in individual cages once daily and presented with a drop of jam. Five days later, the jam was again offered with admixed drug. Mice ingested it in less than 5 min, with latency times below 1 min, confirming the suitability of the administration method.


Subject(s)
Administration, Oral , Laboratory Animal Science/methods , Models, Animal , Animals , Female , Male , Mice
13.
Exp Anim ; 70(3): 372-377, 2021 Aug 06.
Article in English | MEDLINE | ID: mdl-33840658

ABSTRACT

It is known that administering a gavage to rodents evokes a cardiac reflex, due to gastrointestinal stimulation. Consequently, it is difficult to evaluate changes in hemodynamics after a single oral dose of a pungent or astringent, which alters the circulation by increasing sympathetic activity. In the present study, we developed a method for administering a gavage without significantly affecting hemodynamics measurements. We marked a gastric tube at 10 cm from the tip, to mark the distance from the oral cavity to the stomach body of Wistar male rats. Rats were intubated under urethane anesthesia.After 10-15 min of stabilization, we measured the mean blood pressure (MBP), heart rate (HR), and blood flow (BF) in the cremaster arteriole under two different conditions; condition 1: a pointed gastric tube, room temperature distilled water, and injected at normal speed (approximately 3 ml/min); condition 2: a rounded gastric tube, 37°C distilled water, and injection at 1.0 ml/min. Under condition 1, we observed striking hemodynamic alterations, due to the somatic afferent reflex. In contrast, under condition 2, these hemodynamic changes were nearly eliminated. In addition, we could clearly detect hemodynamic changes in rats after a single gavage treatment of pungent (capsaicin) or astringent (cinnamtannin A2). We observed transient increases in the HR and MBP soon after treatment with capsaicin. Moreover, cremasteric BF was elevated with cinnamtannin A2. These results confirmed the utility of the gavage method developed in this study.


Subject(s)
Hemodynamics , Intubation, Gastrointestinal/methods , Laboratory Animal Science/methods , Rats/blood , Animals , Male , Rats, Wistar
14.
STAR Protoc ; 2(2): 100536, 2021 06 18.
Article in English | MEDLINE | ID: mdl-34027493

ABSTRACT

Gnotobiology has revolutionized the study of microbiota-host interactions. This protocol explains how to generate, maintain, and monitor gnotobiotic mice. Three monitoring methods are presented and compared: bacterial culture, microscopy to visualize the presence (or absence) of bacteria using Gram staining or DNA staining, and 16S rRNA gene amplification and sequencing. The generation and maintenance of gnotobiotic animals should be performed in a germ-free and gnotobiotic facility to guarantee sterility and precision of gnotobiotic conditions. For complete details on the use and execution of this protocol, please refer to McDonald et al., 2020.


Subject(s)
Bacteria , Germ-Free Life , Laboratory Animal Science , Animals , Bacteria/genetics , Bacteria/isolation & purification , Bacteriological Techniques , DNA, Bacterial/genetics , Laboratory Animal Science/methods , Laboratory Animal Science/standards , Mice , RNA, Ribosomal, 16S/genetics , Specific Pathogen-Free Organisms
15.
Mamm Genome ; 21(5-6): 224-30, 2010 Jun.
Article in English | MEDLINE | ID: mdl-20411264

ABSTRACT

Laboratory Animal Management Assistant (LAMA) is an internet-based system for tracking large laboratory mouse colonies. It has a user-friendly interface with powerful search capabilities that ease day-to-day tasks such as tracking breeding cages and weaning litters. LAMA was originally developed to manage hundreds of new mouse strains generated by a large functional genomics program, the Pleiades Promoter Project ( http://www.pleiades.org ). The software system has proven to be highly flexible, suitable for diverse management approaches to mouse colonies. It allows custom tagging and grouping of animals, simplifying project-specific handling and access to data. Finally, LAMA was developed in close collaboration with mouse technicians to ease the transition from paper- or Excel-based management systems to computerized tracking, allowing data export in a popular spreadsheet format and automatic printing of cage cards. LAMA is an open-access software tool, freely available to the research community at http://launchpad.net/mousedb .


Subject(s)
Mice, Inbred Strains , Software , Animals , Database Management Systems , Databases, Genetic , Genomics/methods , Laboratory Animal Science/methods , Mice , Research
16.
Lab Anim (NY) ; 39(6): 175-6, 2010 Jun.
Article in English | MEDLINE | ID: mdl-20485356

ABSTRACT

Though not as common as small rodents in laboratory settings, bats are being increasingly used in research studies. Knowledge of proper blood sampling techniques is essential for care and management of bats.


Subject(s)
Chiroptera/physiology , Laboratory Animal Science/methods , Phlebotomy/veterinary , Veterinary Medicine/methods , Animals , Axillary Vein , Male , Phlebotomy/methods , Restraint, Physical/veterinary , Saphenous Vein , Specimen Handling/veterinary
17.
Lab Anim (NY) ; 39(1): 14-5, 2010 Jan.
Article in English | MEDLINE | ID: mdl-20023676

ABSTRACT

If a rabbit is ill or will be undergoing certain types of surgery, it may need to be fed using a nasogastric tube. Nasogastric intubation is easy and is an effective means of delivering nutrition and fluids when other feeding methods are not feasible. This column describes how to place a nasogastric tube in a rabbit.


Subject(s)
Intubation, Gastrointestinal/veterinary , Laboratory Animal Science/methods , Veterinary Medicine/methods , Animals , Intubation, Gastrointestinal/adverse effects , Intubation, Gastrointestinal/instrumentation , Intubation, Gastrointestinal/methods , Rabbits
18.
Lab Anim (NY) ; 39(1): 23-5, 2010 Jan.
Article in English | MEDLINE | ID: mdl-20023678

ABSTRACT

Imaging studies that use rodents sometimes involve intraperitoneal administration of pharmacological compounds. To facilitate such studies, the authors developed a simple and easily mastered technique for placing an intraperitoneal catheter in a conscious mouse. This technique eliminates the need to remove the animal from the scanner to administer a drug through the intraperitoneal route.


Subject(s)
Catheterization/methods , Catheters, Indwelling , Laboratory Animal Science/methods , Pharmaceutical Preparations/administration & dosage , Animals , Injections, Intraperitoneal , Magnetic Resonance Imaging , Mice , Models, Animal , Peritoneal Cavity , Positron-Emission Tomography
19.
Lab Anim (NY) ; 39(5): 143-8, 2010 May.
Article in English | MEDLINE | ID: mdl-20410898

ABSTRACT

Abdominal lavage is used in laboratory rodents for a variety of applications but carries an inherent risk of abdominal organ laceration; therefore, personnel carrying out this procedure must have considerable expertise. In this paper, the authors describe an improved method for delivering sterile media to and collecting peritoneal fluids from dark-clawed Mongolian gerbils (Meriones unguiculatus) that had been peritoneally infected with filarial nematode parasites (genus Brugia). To carry out this gravity-assisted technique, the authors used a catheter to introduce sterile media into the peritoneal cavity of each gerbil and then to passively drain peritoneal fluid and larval worms for collection. Average fluid recovery was consistently greater when using this gravity-assisted method than when using aspiration. Larval parasites were recovered by both methods. To recover large volumes of fluid using the standard method of abdominal lavage, personnel typically must euthanize rodents. This gravity-assisted technique allows researchers to collect large numbers of parasite larvae without euthanizing gerbils.


Subject(s)
Catheterization/veterinary , Gerbillinae/physiology , Laboratory Animal Science/instrumentation , Peritoneal Lavage/instrumentation , Animals , Animals, Laboratory , Brugia/isolation & purification , Disease Models, Animal , Elephantiasis, Filarial/parasitology , Laboratory Animal Science/methods , Male , Parasitic Diseases, Animal/parasitology , Peritoneal Lavage/methods , Specimen Handling
20.
ALTEX ; 37(2): 167-186, 2020.
Article in English | MEDLINE | ID: mdl-32242634

ABSTRACT

Seven years after the last release, the European Commission has again collated and released data on laboratory animal use. The new report is the first to correspond to the requirements of the new Directive 2010/63/EU. Beside minor problems in reporting, the new reporting format is a major step forward, with additional new categories like severity allowing insight into animal use related questions that goes far beyond the previous reports. An in-depth analysis confirms a slight decrease in animal use from 2015 to 2017, but also compared to the 2005, 2008 and 2011 reports, though the new reporting scheme makes this comparison difficult. Notable success is evident for replacing rabbit pyrogen testing but, in general, the implementation of accepted alternative methods lags behind expec-tations. Beside the roughly 10 million animals per year covered in the report, about 8 million animals were identified that fall under the Directive but are not included in this number. Their omission downplays the impact of REACH on animal use. The report, second to none in its detail internationally, represents an important instrument for benchmarking and strategi-cally focusing activities in the 3Rs.


Subject(s)
Animal Testing Alternatives/statistics & numerical data , European Union , Laboratory Animal Science/methods , Laboratory Animal Science/statistics & numerical data , Animals , Benchmarking , Data Interpretation, Statistical
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