The Wistar Kyoto Rat: A Model of Depression Traits.
The Wistar Kyoto Rat: A Model of Depression Traits.
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DOI:
10.2174/1570159x21666221129120902
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发表时间:
2023
影响因子:
5.3
通讯作者:
中科院分区:
文献类型:
--
作者:
There is an ongoing debate about the value of animal research in psychiatry with valid lines of reasoning stating the limits of individual animal models compared to human psychiatric illnesses. Human depression is not a homogenous disorder; therefore, one cannot expect a single animal model to reflect depression heterogeneity. This limited review presents arguments that the Wistar Kyoto (WKY) rats show intrinsic depression traits. The phenotypes of WKY do not completely mirror those of human depression but clearly indicate characteristics that are common with it. WKYs present despair-like behavior, passive coping with stress, comorbid anxiety, and enhanced drug use compared to other routinely used inbred or outbred strains of rats. The commonly used tests identifying these phenotypes reflect exploratory, escape-oriented, and withdrawal-like behaviors. The WKYs consistently choose withdrawal or avoidance in novel environments and freezing behaviors in response to a challenge in these tests. The physiological response to a stressful environment is exaggerated in WKYs. Selective breeding generated two WKY substrains that are nearly isogenic but show clear behavioral differences, including that of depression-like behavior. WKY and its substrains may share characteristics of subgroups of depressed individuals with social withdrawal, low energy, weight loss, sleep disturbances, and specific cognitive dysfunction. The genomes of the WKY and WKY substrains contain variations that impact the function of many genes identified in recent human genetic studies of depression. Thus, these strains of rats share characteristics of human depression at both phenotypic and genetic levels, making them a model of depression traits.
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影响因子:
3.6
作者:
Yaroslavsky, Irene;Tejani-Butt, Shanaz M.
通讯作者:
Tejani-Butt, Shanaz M.
影响因子:
3.3
作者:
Ortiz AN;Oien DB;Moskovitz J;Johnson MA
通讯作者:
Johnson MA
影响因子:
3
作者:
Kim S;Gacek SA;Mocchi MM;Redei EE
通讯作者:
Redei EE
影响因子:
5
作者:
Jenz ST;Goodyear CD;TSgt Graves PR;Goldstein S;Shia MR;Redei EE
通讯作者:
Redei EE
DOI:
10.1002/dad2.12116
发表时间:
2020
期刊:
Alzheimer's & dementia (Amsterdam, Netherlands)
影响因子:
--
作者:
Kaur D;Bucholc M;Finn DP;Todd S;Wong-Lin K;McClean PL
通讯作者:
McClean PL