Qing YU, Xue JIANG, Qin LI. Hyperactivity of hypothalamus-pituitary-adrenalaxis is associated with reduced expression of glucocorticoid steroid receptor in a rat model of anxiety[J]. Journal of Third Military Medical University, 2017, 39(14): 1464-1468.
DOI:
Qing YU, Xue JIANG, Qin LI. Hyperactivity of hypothalamus-pituitary-adrenalaxis is associated with reduced expression of glucocorticoid steroid receptor in a rat model of anxiety[J]. Journal of Third Military Medical University, 2017, 39(14): 1464-1468. DOI: 10.16016/j.1000-5404.201611238.
Hyperactivity of hypothalamus-pituitary-adrenalaxis is associated with reduced expression of glucocorticoid steroid receptor in a rat model of anxiety
To determine whether the hyperactivity of the hypothalamus-pituitary-adrenal(HPA) axis in response to stress is associated with the hyperfunction of the HPA axis or with the feedback regulation of glucocorticoid steroid receptor (GR) expression in rat model of anxiety.
Methods
2
Healthy male SD rats were randomly divided into control group(
n
=20) without any stimulation and anxiety model group(
n
=26) exposed to unpredictable emotional stress. All the rats were weighed once a week and at the end of the stimulus
and the behavioral changes of the rats were observed in elevated plus-maze (EPM) and open-f
ield tests. Serum levels of adrenocorticotropic hormone(ACTH) and corticosterone were measured in the rats following stimulation with open-field and EPM as the stressors
and the expression of GR in the hippocampal
hypothalamic
pituitary and adrenal tissues was detected with Western blotting.
Results
2
The rat models of anxiety showed a significantly lower rate of body weight increase than the control rats (
P
<
0.01). The rats with anxiety exhibited a significantly lower number and a lower percentage of open arm entry
shorter and lower percentage of retention time in the open arm (
P
<
0.01)
shorter total distance and central time
and lower central distance percentage in the open-field test (
P
<
0.05
P
<
0.01). No significant differences were found in the serum levels of ACTH or corticosterone between the 2 groups at baseline
but after stress stimulation
their levels became obviously higher in the model group than in the control group(
P
<
0.01). The protein level of GR was significantly reduced in the hypothalamic(
P
<
0.05) and adrenal tissues (
P
<
0.01) in the model group as compared with the control group
but no significant difference was found in GR level in the pituitary tissue between the 2 groups (
P
>
0.05).
Conclusion
2
The hyperactivity of the HPA axis under stress is associated with the attenuation of GR-mediated negative feedback regulation in rat models of anxiety.
关键词
Keywords
references
GWYNN R C, MCQUISTION H L, MCVEIGH K H, et al . Prevalence,diagnosis,and treatment of depression and generalized anxiety disorder in a diverse urban community[J]. Psychiatr Serv, 2008, 59(6): 641-647. DOI: 10.1176/appi.ps.59.6.641.
KENNY R, DINAN T, CAI G, et al . Effects of mild calorie restriction on anxiety and hypothalamic-pituitary-adrenal axis response to stress in the male rat[J]. Physiol Rep, 2014, 2(3): e00265. DOI: 10.1002/phy2.265.
LOK A, MOCKING R J, RUH H G, et al . Longitudinal hypothalamic-pituitary-adrenal axis trait and state effects in recurrent depression [J]. Psychoneuroendocrinology, 2012, 37(7): 892-902. DOI: 10.1016/j.psyneuen.2011.10.005.
MINTZER J, O’NEILL C. Depression in Alzheimer’s disease: consequence or contributing factor?[J]. Expert Rev Neurother, 2011, 11(11): 1501-1503. DOI: 10.1586/ern.11.145.
JACOB E L, GATTO N M, THOMPSON A, et al . Occurrence of depression and anxiety prior to Parkinson’s disease [J].Parkinsonism Relat Disord, 2010, 16(9): 576-581.DOI: 10.1016/j.parkreldis.2010.06.014.
ROMAN O, SERES J, POMETLOVA M, et al . Neuroendocrine or behavioral effects of acute or chronic emotional stress in Wistar Kyoto(WKY)and spontaneously hypertensive rats[J]. Endocr Regul, 2014, 38(4): 151-155.
DU X, PANG T Y. Is Dysregulation of the HPA-Axis a Core Pathophysiology Mediating Co-Morbid Depression in Neurodegenerative Diseases? [J]. Frontiers in Psychiatry, 2015, 6(32): 32.DOI: 10.3389/fpsyt.2015.00032.
CHEN J, WANG Z Z, ZUO W, et al .Effects of chronic mild stress on behavioral and neurobiological parameters-Role of glucocorticoid[J]. Horm Behav, 2016, 2(78): 150-159. DOI: 10.1016/j.yhbeh.2015.11.006.
ELNAZER H Y, BALDWIN D S. Investigation of cortisol levels in patients with anxiety disorders: a structured review [J]. Curr Top Behav Neurosci, 2014, 18: 191-216. DOI: 10.1007/7854_2014_299.
GHOSAL S, BUNDZIKOVA-OSACKA J, DOLGAS C M, et al . Glucocorticoid receptors in the nucleus of the solitary tract(NTS) decrease endocrine and behavioral stress responses[J]. Psychoneuroendocrinology, 2014, 45: 142-153. DOI: 10.1016/j.psyneuen.2014.03.018.
KESSLER R C, KELLER M B, WITTCHEN H U.The epidemiology of generalized anxiety disorder[J].Psychiatr Clin North Am, 2001, 24(1): 19-39. DOI: 10.1016/s0193-953x(05)70204-5.
WANG D C, CHEN T J, LIN M L, et al . Exercise prevents the increased anxiety-like behavior in lactational di-(2-ethylhexyl) phthalate-exposed female rats in late adolescence by improving the regulation of hypothalamus-pituitary-adrenal axis[J]. Horm Behav, 2014, 66(4): 674-684. DOI: 10.1016/j.yhbeh.2014.09.010.
KOLBER B J, WIECZOREK L,.MUGLIA L J. Hypothalamic-pituitary-adrenal axis dysregulation and behavioral analysis of mouse mutants with altered glucocorticoid or mineralocorticoid receptor function[J].Stress, 2008, 11(5): 321-338. DOI: 10.1080/10253890701821081.
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