Laboratory Syrian hamster

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Normal gait of an individual lab-bred hamster. Certain tests may change normal behavior.

Syrian hamsters (Mesocricetus auratus) are one of several rodents used in animal testing. Syrian hamsters are used to model human medical conditions including various cancers, metabolic diseases, non-cancer respiratory diseases, cardiovascular diseases, infectious diseases, and general health concerns.[1] In 2014, Syrian hamsters accounted for 14.6% of the total animal research participants in the United States covered by the Animal Welfare Act.[2]

Use in research[]

Since 1972 the use of hamsters in animal testing research has declined.[3] In 2014 in the United States, animal research used about 120,000 hamsters, which was 14.6% of the total research animal use (under the Animal Welfare Act which excludes mice, rats, and fish) for that year in that country.[3][2] According to the , a total of 1,931 hamsters were used for research in 2013 in Canada, making them the sixth-most popular rodent after mice (1,233,196), rats (228,143), guinea pigs (20,687), squirrels (4,446) and voles (2,457).[4]

Human medical research[]

Cancer research[]

Humans get lung cancer from tobacco smoking.[5] Syrian hamsters are a model for researching Non-small-cell lung carcinoma, which is one of the types of human lung cancer.[5] In research, when hamsters are injected with the carcinogen NNK several times over six months, they will develop that sort of cancer.[6] In both Syrian hamsters and humans, this cancer is associated with mutations to the KRAS gene.[7] For various reasons, collecting data on the way that Syrian hamsters develop this lung cancer provides insight on how humans develop it.[6]

Oral squamous-cell carcinoma is a common cancer in humans and difficult to treat.[8] Scientists studying this disease broadly accept Syrian hamsters as animal models for researching it.[8] In this research, the hamster is given anesthesia, has its mouth opened to expose the inside of its cheeks, and the researcher brushes the carcinogen DMBA on its cheeks.[8] The scientist can take cell samples from the mouth of the hamster to measure the development of the cancer.[8] This process has good reproducibility.[8] The cancer itself develops tumors in a predictable way starting with hyperkeratosis, then hyperplasia, then dysplasia, then carcinoma.[8] In humans with this cancer there is increased ErbB2 production of receptor tyrosine kinase and Syrian hamsters with this cancer also have increased levels of that kinase.[9] As the tumor develops in the hamster, they also have increased gene expression in p53 and c-myc which is similar to human cancer development.[10] Because hamsters develop this cancer so predictably, researchers are comfortable in using hamsters in research on prevention and treatment.[11]

There is scientific and social controversy about the virus SV40 causing cancers in human.[12] Leaving that controversy aside, Syrian hamsters injected with SV40 certainly will develop various cancers in predictable ways depending on how they are exposed to the virus.[13] The hamster has been used as a research model to clarify what SV40 does in humans.[14]

The golden hamster can contract contagious reticulum cell sarcoma[15] which can be transmitted from one golden hamster to another by means of the bite of the mosquito Aedes aegypti.[16]

Metabolic disorders[]

Syrian hamsters are susceptible to many metabolic disorders which affect humans.[17] Because of this, hamsters are an excellent animal model for studying human metabolic disorder.[17]

Gallstones may be induced in Syrian hamsters by giving the hamster excess dietary cholesterol or sucrose.[18] Hamsters metabolize cholesterol in a way that is similar to humans.[19] Different sorts of fats are more or less likely to produce gallstones in hamsters.[20] The gender differences in gallstone formation in hamsters is significant.[20] Hamsters of different genetic strains have significant differences in susceptibility to forming gallstones.[20]

Diabetes mellitus is studied in various ways using Syrian hamsters. Hamsters which are feed fructose for 7 days get hyperinsulinemia and hyperlipidemia.[21] Such hamsters then have an increase in hepatic lipase and other measurable responses which are useful for understanding diabetes in humans.[21] Streptozotocin or alloxan may be administered to induce chronic diabetes in hamsters.[21]

Atherosclerosis may be studied with Syrian hamsters because both organisms have similar lipid metabolism.[22] Hamsters develop atherosclerosis as a result of dietary manipulation.[22] Hamsters develop atherosclerotic plaques as humans do.[22]

Non-cancer respiratory disease[]

Smoke inhalation can be studied on Syrian hamsters by putting the hamster in a laboratory smoking machine.[23] Pregnant hamsters have been used to model the effects of smoking on pregnant humans.[24]

The emphysema component of COPD may be induced in hamsters by injecting pancreatic elastase into their tracheas.[25]

Pulmonary fibrosis may be induced in hamsters by injecting bleomycin into their tracheas.[26][27]

Cardiovascular[]

Cardiomyopathy in hamsters is an inherited condition and there are genetic lines of hamsters which are bred to retain this gene so that they may be used to study the disease.[28]

Microcirculation may be studied in hamster cheek pouches.[29] The pouches of hamsters are thin, easy to examine without stopping bloodflow, and highly vascular.[29] When examined, the cheek pouch is pulled through the mouth while being grasped with forceps.[30] At this point the cheek is everted and can be pinned onto a mount for examination.[30]

Reperfusion injury may be studied with everted hamster pouches also.[31] To simulate reperfusion, one method is to tie a cuff around the pouch to restrict blood flow and cause ischemia.[32] Another method could be to compress the veins and arteries with microvascular clips which do not cause trauma.[33] In either case, after about an hour of restricting the blood, the pressure is removed to study how the pouch recovers.[31]

Several inbred strains of hamsters have been developed as animal models for human forms of dilated cardiomyopathy. The gene responsible for hamster cardiomyopathy in a widely studied inbred hamster strain, BIO14.6, has been identified as being delta-sarcoglycan.[34] Pet hamsters are also potentially prone to cardiomyopathy, which is a not infrequent cause of unexpected sudden death in adolescent or young adult hamsters.

Infection research[]

Syrian hamsters have been infected with a range of disease causing agents to study both the disease and the cause of the disease.

Hantavirus pulmonary syndrome is a medical condition in humans caused by any of the Hantavirus species. Syrian hamsters easily contract Hantavirus species, but they do not get the same symptoms as humans, and the same infection that is deadly in humans have effects ranging from nothing to flu to death in Syrian hamsters.[35] Because hamsters become easily infected, they are used to study the pathogenesis of Hantavirus.[36] Andes virus and Maporal viruses infect hamsters and cause pneumonia and edema.[37][38] The Sin Nombre virus and Choclo virus will infect hamsters but not cause any disease.[35][39]

SARS coronavirus causes severe acute respiratory syndrome in humans. Syrian hamsters may be infected with the virus, and like humans will have viral replication and lesions in the respiratory tract which can be examined with histopathological tests.[40] However, hamsters do not develop clinical symptoms of the disease.[41] Hamsters might be used to study the infection process.[42]

Leptospira viruses cause Leptospirosis in humans and similar symptoms in Syrian hamsters.[40][43] Syrian hamsters are used to test drugs to treat the disease.[44]

Bacteria which have been studied by infection Syrian hamsters with them include Leptospira, Clostridium difficile, Mycoplasma pneumoniae, and Treponema pallidum.[45]

Parasites which have been studied by infecting Syrian hamsters with them include Toxoplasma gondii, Babesia microti, Leishmania donovani, Trypanosoma cruzi, Opisthorchis viverrini, Taenia, Ancylostoma ceylanicum, and Schistosoma.[46]

Syrian hamsters are infected with scrapie so that they get transmissible spongiform encephalopathy. [47]

In March 2020, researchers from the University of Hong Kong have shown that Syrian hamsters could be a model organism for COVID-19 research.[48]

Other medical conditions[]

Scientists use male hamsters to study the effects of steroids on male behavior.[49] The behavior of castrated hamsters is compared to typical male hamsters.[49] Castrated hamsters are then given steroids and their behavior noted.[49] Some steroid treatments will cause castrated hamsters to do behaviors that typical male hamsters do.[49]

Poor nutrition may cause female infertility in mammals.[50] When hamsters do not have enough of the right food, they have fewer estrous cycles.[51] Studies in hamsters identify the nutritional needs for maintaining fertility.[52]

Syrian hamsters are used to study how NSAIDs can cause reactive gastropathy.[53] One way to study is to inject hamsters with indometacin, which causes an ulcer within 1–5 hours depending on the dose.[54] If repeatedly given doses, hamsters get severe lesions and die within 5 days from peptic ulcers in their pyloric antrum.[54] A model for creating a chronically ill hamster which will not die from the ulcers is to give naproxen by gavage.[55] When the hamster is chronically ill, it can be used to test anti-ulcer drugs.[55]

Syrian hamsters are also widely used in research into alcoholism, by virtue of their large livers, and ability to metabolise high doses.[56]

Research on Syrian hamsters themselves[]

In captivity, golden hamsters follow well-defined daily routines of running in their hamster wheel, which has made them popular subjects in circadian rhythms research. For example, Martin Ralph, Michael Menaker, and colleagues used this behavior to provide definitive evidence that the suprachiasmatic nucleus in the brain is the source of mammalian circadian rhythms.[57]

Hamsters have a number of fixed action patterns that are readily observed, including scent-marking and body grooming, which is of interest in the study of animal behavior.

Scientific studies of animal welfare concerning captive golden hamsters have shown they prefer to use running wheels of large diameters (35 cm diameter was preferred over 23 cm,[58] and 23  cm over 17.5  cm,[59]), and that they prefer bedding material which allows them to build nests, if nesting material is not already available.[60] They prefer lived-in bedding (up to two weeks old – longer durations were not tested) over new bedding, suggesting they may prefer bedding changes at two-week intervals rather than weekly or daily.[61] They also prefer opaque tubes closed at one end, 15 cm in diameter, to use as shelter in which to nest and sleep.[62]

Notes[]

  1. ^ Valentine 2012, pp. 875–898.
  2. ^ Jump up to: a b Speaking of Research (2015), US Statistics, Speaking of Research, retrieved 18 April 2016
  3. ^ Jump up to: a b Smith 2012, p. 750.
  4. ^ CCAC – CCAC Animal Data Report 2013
  5. ^ Jump up to: a b Valentine 2012, p. 877 cites
  6. ^ Jump up to: a b Valentine et al. 2012, p. 877.
  7. ^ Valentine 2012, p. 877 cites
    • Oreffo, VI; Lin, HW; Gumerlock, PH; Kraegel, SA; Witschi, H (1992). "Mutational analysis of a dominant oncogene (c-Ki-ras-2) and a tumor suppressor gene (p53) in hamster lung tumorigenesis". Molecular Carcinogenesis. 6 (3): 199–202. doi:10.1002/mc.2940060305. PMID 1445620.
  8. ^ Jump up to: a b c d e f Valentine 2012, pp. 877–878 cites
    • Vairaktaris, E; Spyridonidou, S; Papakosta, V; Vylliotis, A; Lazaris, A; Perrea, D; Yapijakis, C; Patsouris, E (April 2008). "The hamster model of sequential oral oncogenesis". Oral Oncology. 44 (4): 315–24. doi:10.1016/j.oraloncology.2007.08.015. PMID 18061531.
  9. ^ Valentine 2012, pp. 877–878 cites
    • Werkmeister, R; Brandt, B; Joos, U (January 2000). "Clinical relevance of erbB-1 and -2 oncogenes in oral carcinomas". Oral Oncology. 36 (1): 100–5. doi:10.1016/s1368-8375(99)00069-x. PMID 10889928.
  10. ^ Valentine 2012, pp. 877–878 cites
    • Papakosta, V; Vairaktaris, E; Vylliotis, A; Derka, S; Nkenke, E; Vassiliou, S; Lazaris, A; Mourouzis, C; Rallis, G; Spyridonidou, S; Anagnostopoulou, S; Perrea, D; Donta, I; Yapijakis, C; Patsouris, E (n.d.). "The co-expression of c-myc and p53 increases and reaches a plateau early in oral oncogenesis". Anticancer Research. 26 (4B): 2957–62. PMID 16886620.
  11. ^ Valentine 2012, p. 877-878 cites
    • Shklar, G (December 1999). "Development of experimental oral carcinogenesis and its impact on current oral cancer research". Journal of Dental Research. 78 (12): 1768–72. doi:10.1177/00220345990780120101. PMID 10598904.
  12. ^ Valentine 2012, pp. 877–878 cites
    • Pershouse, Mark A.; Heivly, Shane; Girtsman, Teri (2006). "The Role of SV40 in Malignant Mesothelioma and Other Human Malignancies". Inhalation Toxicology. 18 (12): 995–1000. doi:10.1080/08958370600835377. ISSN 0895-8378. PMID 16920674.
  13. ^ Valentine 2012, p. 878 cites
  14. ^ Valentine et al. 2012, p. 878.
  15. ^ Copper, H. L.; MacKay, C. M.; Banfield, W. G. (1 October 1964). "Chromosome Studies of a Contagious Reticulum Cell Sarcoma of the Syrian Hamster". Journal of the National Cancer Institute. 33: 691–706. doi:10.1093/jnci/33.4.691. PMID 14220251.
  16. ^ Banfield, William G.; Woke, P. A.; MacKay, C. M.; Cooper, H. L. (28 May 1965). "Mosquito Transmission of a Reticulum Cell Sarcoma of Hamsters". Science. 148 (3674): 1239–1240. Bibcode:1965Sci...148.1239B. doi:10.1126/science.148.3674.1239. PMID 14280009.
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    • Ginsberg, HN (July 1996). "Diabetic dyslipidemia: basic mechanisms underlying the common hypertriglyceridemia and low HDL cholesterol levels". Diabetes. 45 Suppl 3: S27–30. doi:10.2337/diab.45.3.s27. PMID 8674885.
    • Gotto AM, Jr (14 December 1992). "Hypertriglyceridemia: risks and perspectives". The American Journal of Cardiology. 70 (19): 19H–25H. doi:10.1016/0002-9149(92)91086-j. PMID 1466313.
    • Laakso, Markku (2009). "Lipids and Lipoproteins as Risk Factors for Coronary Heart Disease in Non-insulin-dependent Diabetes Mellitus". Annals of Medicine. 28 (4): 341–345. doi:10.3109/07853899608999091. ISSN 0785-3890. PMID 8862689.
    • Lamarche, B; Lewis, GF (June 1998). "Atherosclerosis prevention for the next decade: risk assessment beyond low density lipoprotein cholesterol". The Canadian Journal of Cardiology. 14 (6): 841–51. PMID 9676170.
  18. ^ Valentine et al. 2012, p. 880 cites Trautwein, EA; Siddiqui, A; Hayes, KC (September 1999). "Characterization of the bile acid profile in developing male and female hamsters in response to dietary cholesterol challenge". Comparative Biochemistry and Physiology A. 124 (1): 93–103. doi:10.1016/s1095-6433(99)00095-1. PMID 10605070.
    • Cohen, BI; Matoba, N; Mosbach, EH; McSherry, CK (February 1989). "Dietary induction of cholesterol gallstones in hamsters from three different sources". Lipids. 24 (2): 151–6. doi:10.1007/bf02535254. PMID 2755304.
  19. ^ Khallou, J; Riottot, M; Parquet, M; Verneau, C; Lutton, C (November 1991). "Biodynamics of cholesterol and bile acids in the lithiasic hamster". The British Journal of Nutrition. 66 (3): 479–92. doi:10.1079/bjn19910049. PMID 1772872.
  20. ^ Jump up to: a b c Valentine 2012, p. 880.
  21. ^ Jump up to: a b c Valentine 2012, p. 881.
  22. ^ Jump up to: a b c Valentine 2012, p. 882.
  23. ^ Valentine 2012, p. 883.
  24. ^ Magers, T; Talbot, P; DiCarlantonio, G; Knoll, M; Demers, D; Tsai, I; Hoodbhoy, T (n.d.). "Cigarette smoke inhalation affects the reproductive system of female hamsters". Reproductive Toxicology (Elmsford, N.Y.). 9 (6): 513–25. doi:10.1016/0890-6238(95)02002-0. PMID 8597648.
  25. ^ Valentine 2012, p. 883 cites
  26. ^ Valentine 2012, p. 884.
  27. ^ Lazo, JS; Hoyt, DG; Sebti, SM; Pitt, BR (1990). "Bleomycin: a pharmacologic tool in the study of the pathogenesis of interstitial pulmonary fibrosis". Pharmacology & Therapeutics. 47 (3): 347–58. doi:10.1016/0163-7258(90)90061-6. PMID 1705351.
  28. ^ Valentine 2012, p. 885.
  29. ^ Jump up to: a b Valentine 2012, p. 885 cites
    • Davis, MJ; Gore, RW (January 1985). "A new preparation for microcirculatory studies of the hamster cheek pouch". The American Journal of Physiology. 248 (1 Pt 2): H143–6. doi:10.1152/ajpheart.1985.248.1.H143. PMID 3881981.
    • Kerger, H; Torres Filho, IP; Rivas, M; Winslow, RM; Intaglietta, M (February 1995). "Systemic and subcutaneous microvascular oxygen tension in conscious Syrian golden hamsters". The American Journal of Physiology. 268 (2 Pt 2): H802–10. doi:10.1152/ajpheart.1995.268.2.H802. PMID 7864208.
    • Klitzman, B; Popel, AS; Duling, BR (January 1983). "Oxygen transport in resting and contracting hamster cremaster muscles: experimental and theoretical microvascular studies". Microvascular Research. 25 (1): 108–31. doi:10.1016/0026-2862(83)90047-x. PMID 6835096.
    • Svensjö, E (December 1990). "The hamster cheek pouch as a model in microcirculation research". The European Respiratory Journal. Supplement. 12: 595s–600s, discussion 600s–601s. PMID 2076153.
  30. ^ Jump up to: a b Davis, MJ; Gore, RW (January 1985). "A new preparation for microcirculatory studies of the hamster cheek pouch". The American Journal of Physiology. 248 (1 Pt 2): H143–6. doi:10.1152/ajpheart.1985.248.1.H143. PMID 3881981.
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  32. ^ Persson, NH; Erlansson, M; Svensjö, E; Takolander, R; Bergqvist, D (1985). "The hamster cheek pouch – an experimental model to study postischemic macromolecular permeability". International Journal of Microcirculation, Clinical and Experimental. 4 (3): 257–63. PMID 2415477.
  33. ^ Bertuglia, S; Marchiafava, PL; Colantuoni, A (June 1996). "Melatonin prevents ischemia reperfusion injury in hamster cheek pouch microcirculation". Cardiovascular Research. 31 (6): 947–52. doi:10.1016/0008-6363(96)00030-2. PMID 8759251.
  34. ^ Nigro, V.; Okazaki, Y; Belsito, A; Piluso, G; Matsuda, Y; Politano, L; Nigro, G; Ventura, C; et al. (1997). "Identification of the Syrian hamster cardiomyopathy gene". Human Molecular Genetics. 6 (4): 601–607. doi:10.1093/hmg/6.4.601. PMID 9097966.
  35. ^ Jump up to: a b Valentine et al. 2012, p. 887.
  36. ^ Hooper, JW; Larsen, T; Custer, DM; Schmaljohn, CS (10 October 2001). "A lethal disease model for hantavirus pulmonary syndrome". Virology. 289 (1): 6–14. doi:10.1006/viro.2001.1133. PMID 11601912.
  37. ^ McElroy, AK; Smith, JM; Hooper, JW; Schmaljohn, CS (15 August 2004). "Andes virus M genome segment is not sufficient to confer the virulence associated with Andes virus in Syrian hamsters". Virology. 326 (1): 130–9. doi:10.1016/j.virol.2004.05.018. PMID 15262501.
  38. ^ Milazzo, ML; Eyzaguirre, EJ; Molina, CP; Fulhorst, CF (15 November 2002). "Maporal viral infection in the Syrian golden hamster: a model of hantavirus pulmonary syndrome". The Journal of Infectious Diseases. 186 (10): 1390–5. doi:10.1086/344735. PMID 12404153.
  39. ^ Eyzaguirre, EJ; Milazzo, ML; Koster, FT; Fulhorst, CF (April 2008). "Choclo virus infection in the Syrian golden hamster". The American Journal of Tropical Medicine and Hygiene. 78 (4): 669–74. doi:10.4269/ajtmh.2008.78.669. PMC 2689364. PMID 18385367.
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  41. ^ Roberts, A; Vogel, L; Guarner, J; Hayes, N; Murphy, B; Zaki, S; Subbarao, K (January 2005). "Severe acute respiratory syndrome coronavirus infection of golden Syrian hamsters". Journal of Virology. 79 (1): 503–11. doi:10.1128/jvi.79.1.503-511.2005. PMC 538722. PMID 15596843.
  42. ^ Schaecher, SR; Stabenow, J; Oberle, C; Schriewer, J; Buller, RM; Sagartz, JE; Pekosz, A (25 October 2008). "An immunosuppressed Syrian golden hamster model for SARS-CoV infection". Virology. 380 (2): 312–21. doi:10.1016/j.virol.2008.07.026. PMC 3722600. PMID 18760437.
  43. ^ Silva, Éverton F.; Santos, Cleiton S.; Athanazio, Daniel A.; Seyffert, Núbia; Seixas, Fabiana K.; Cerqueira, Gustavo M.; Fagundes, Michel Q.; Brod, Claudiomar S.; Reis, Mitermayer G.; Dellagostin, Odir A.; Ko, Albert I. (2008). "Characterization of virulence of Leptospira isolates in a hamster model". Vaccine. 26 (31): 3892–3896. doi:10.1016/j.vaccine.2008.04.085. ISSN 0264-410X. PMC 2519131. PMID 18547690.
  44. ^ Moon, JE; Rivard, RG; Griffith, ME; Ressner, RA; McCall, S; Reitstetter, RE; Hospenthal, DR; Murray, CK (January 2007). "Effect of timing and duration of azithromycin therapy of leptospirosis in a hamster model". The Journal of Antimicrobial Chemotherapy. 59 (1): 148–51. doi:10.1093/jac/dkl453. PMID 17110394.
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  48. ^ Chan JF, Zhang AJ, Yuan S, et al. (March 2020). "Simulation of the clinical and pathological manifestations of Coronavirus Disease 2019 (COVID-19) in golden Syrian hamster model: implications for disease pathogenesis and transmissibility". Clinical Infectious Diseases. doi:10.1093/cid/ciaa325. ISSN 1058-4838. PMC 7184405. PMID 32215622.
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References[]

  • Smith, Gerald D. (2012). "Hamsters – Taxonomy and History". In Suckow, Mark A.; Stevens, Karla A.; Wilson, Ronald P. (eds.). The laboratory rabbit, guinea pig, hamster, and other rodents (1st ed.). Amsterdam: Elsevier Academic Press. pp. 747–753. ISBN 978-0123809209.
  • Valentine, Helen; Daugherity, Erin K.; Singh, Bhupinder; Maurer, Kirk J. (2012). "The Experimental Use of Syrian Hamsters". In Suckow, Mark A.; Stevens, Karla A.; Wilson, Ronald P. (eds.). The laboratory rabbit, guinea pig, hamster, and other rodents (1st. ed.). Amsterdam: Elsevier Academic Press. pp. 875–898. ISBN 978-0123809209.
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