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Animals · Animal ethology · Comparative psychology · Animal models · Outline · Index


Animal model refers to the induction in a non-human animal a disease, psychological or psychopathological process that is similar to a human condition. The use of model organisms allows researchers to investigate processes and disease states in ways which would be inaccessible in a human patient, performing procedures on the non-human animal that imply a level of harm that would not be considered ethical to inflict on a human.

In order to serve as a useful model, a modeled disease must be similar in etiology (mechanism of cause) and function to the human equivalent. Animal models are used to learn more about a disease, its diagnosis and its treatment. For instance, behavioral analogues of anxiety or pain in laboratory animals can be used to screen and test new drugs for the treatment of these conditions in humans.

The increase in knowledge of the genomes of non-human primates and other mammals that are genetically close to humans is allowing the production of genetically engineered animal tissues, organs and even animal species which express human diseases, providing a more robust model of human diseases in an animal model.

Animal models observed in the sciences of psychology and sociology are often termed animal models of behavior.

Taxonomic human equivalence[]

Whereas a mouse, dog, or pig may serve as a mammalian animal model, a baboon or macaque may serve as a less inclusive primate animal model.[1] An animal model for vertebrates is the zebrafish.[2][3]

File:Zebrafisch.jpg

Danio rerio, better known as the zebrafish

Disease models[]

Animal models serving in research may have an existing, inbred or induced disease or injury that is similar to a human condition. These test conditions are often termed as animal models of disease. The use of animal models allows researchers to investigate disease states in ways which would be inaccessible in a human patient, performing procedures on the non-human animal that imply a level of harm that would not be considered ethical to inflict on a human.[citation needed]

To serve as a useful model, a modeled disease must be similar in etiology (mechanism of cause) and function to the human equivalent. Animal models are used to learn more about a disease, its diagnosis and its treatment. For instance, behavioral analogues of anxiety or pain in laboratory animals can be used to screen and test new drugs for the treatment of these conditions in humans. A 2000 study found that animal models concorded (coincided on true positives and false negatives) with human toxicity in 71% of cases, with 63% for nonrodents alone and 43% for rodents alone.[4]

Animal models of disease can be spontaneous (naturally occurring in animals), or be induced by physical, chemical or biological means. For example,animal models of interest to psychologists include:

The increase in knowledge of the genomes of non-human primates and other mammals that are genetically close to humans is allowing the production of genetically engineered animal tissues, organs and even animal species which express human diseases, providing a more robust model of human diseases in an animal model.

Behavioral sciences[]

Animal models observed in the sciences of psychology and sociology are often termed animal models of behavior. It is difficult to build an animal model that perfectly reproduces the symptoms of depression in patients. However, depression, as other mental disorders, consists of endophenotypes [11] that can be reproduced independently and evaluated in animals. An ideal animal model offers an opportunity to understand molecular, genetic and epigenetic factors that may lead to depression. By using animal models, the underlying molecular alterations and the causal relationship between genetic or environmental alterations and depression can be examined, which would afford a better insight into pathology of depression. In addition, animal models of depression are indispensable for identifying novel therapies for depression.[citation needed]

Genetics[]

In quantitative genetics, the term animal model usually refers to a statistical model in which phenotypic variance is compartmentalised into environmental, genetic and sometimes maternal effects. Such animal models are also known as "mixed models".[citation needed]

Criticisms[]

Many animal models serving as test subjects in biomedical research, such as rats and mice, may be selectively sedentary, obese and glucose intolerant. This may confound their use to model human metabolic processes and diseases as these can be affected by dietary energy intake and exercise.[12]

Animal models of psychiatric illness give rise to other concerns. Qualitative assessments of behavior are too often subjective. This would lead the investigator to observe what they want to observe in subjects, and to render conclusions in line with their expectations. Also, the imprecise diagnostic criteria for psychiatric illnesses inevitably lead to problems modeling the condition; e.g., since a person with major depressive disorder may experience weight loss or weight gain, insomnia or hypersomnia, we cannot with any certainty say that a rat with insomnia and weight loss is depressed. Furthermore, the complex nature of psychiatric conditions makes it difficult/impossible to translate human behaviors and deficits; e.g., language deficit plays a major role in autistic spectrum disorders, but – since rodents do not have language – it is not possible to develop a language-impaired "autistic" mouse.[citation needed]

In addition to the myriad ethical concerns of using animals in biomedical research, animal studies of psychiatric illness raise further concerns about the pain and suffering inflicted on the test subjects. While some scientists argue that care is taken to prevent unnecessary suffering in animal experiments, suffering is an inherent aspect of modeling distressful psychiatric conditions (e.g., anxiety, depression, posttraumatic stress disorder).[citation needed]

References[]

  1. PMID 19507247 (PMID 19507247)
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  4. Olson H, Betton G, Robinson D, et al. (August 2000). Concordance of the toxicity of pharmaceuticals in humans and in animals. Regul. Toxicol. Pharmacol. 32 (1): 56–67.
  5. White HS (1997). Clinical significance of animal seizure models and mechanism of action studies of potential antiepileptic drugs. Epilepsia 38 Suppl 1: S9–17.
  6. Bolton C (2007). The translation of drug efficacy from in vivo models to human disease with special reference to experimental autoimmune encephalomyelitis and multiple sclerosis. Inflammopharmacology 15 (5): 183–7.
  7. Leker RR, Constantini S (2002). Experimental models in focal cerebral ischemia: are we there yet?. Acta Neurochir. Suppl. 83: 55–9.
  8. Wang J, Fields J, Doré S. (2008). The development of an improved preclinical mouse model of intracerebral hemorrhage using double infusion of autologous whole blood. Brain Res 1222: 214–21.
  9. Rynkowski MA, Kim GH, Komotar RJ, et al. (2008). A mouse model of intracerebral hemorrhage using autologous blood infusion. Nat Protoc 3 (1): 122–8.
  10. Homo-Delarche F, Drexhage HA (2004). Immune cells, pancreas development, regeneration and type 1 diabetes. Trends Immunol. 25 (5): 222–9.
  11. Hasler, G. et al. (2004) Discovering endophenotypes for major depression. Neuropsychopharmacology 29, 1765–1781
  12. Martin B, Ji S, Maudsley S, Mattson MP (2010). "Control" laboratory rodents are metabolically morbid: Why it matters.. Proc Natl Acad Sci U S A 107 (14): 6127–6133.

Research by problem[]

Research by animal[]

See also[]

External links[]






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