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慢性应激抑制雄性大鼠下丘脑-垂体-甲状腺轴和棕色脂肪组织对急性冷暴露的反应。

Chronic stress inhibits hypothalamus-pituitary-thyroid axis and brown adipose tissue responses to acute cold exposure in male rats.

机构信息

Departamento de Genética del Desarrollo y Fisiología Molecular, Instituto de Biotecnología, Universidad Nacional Autónoma de México (UNAM), Cuernavaca, México.

出版信息

J Endocrinol Invest. 2021 Apr;44(4):713-723. doi: 10.1007/s40618-020-01328-z. Epub 2020 Jul 30.

Abstract

PURPOSE

Cold exposure activates the hypothalamus-pituitary-thyroid (HPT) axis, response blunted by previous acute stress or corticosterone administration. Chronic stressors can decrease serum T3 concentration, and thyrotropin-releasing hormone (Trh) expression in the paraventricular nucleus (PVN), but impact on the response to cold is unknown; this was studied in rats submitted to daily repeated restraint (rRes) that causes habituation of hypothalamus-pituitary-adrenal (HPA) axis response, or to chronic variable stress (CVS) that causes sensitization and hyperreactivity.

METHODS

Wistar male adult rats were submitted to rRes 30 min/day, or to CVS twice a day, for 15 days. On day 16, rats were exposed 1 h to either 5 or 21 °C. Parameters of HPT and HPA axes activity and of brown adipose tissue (BAT) cold response were measured; gene expression in PVN and BAT, by RT-PCR; serum hormone concentration by radioimmunoassay or ELISA.

RESULTS

Compared to naïve animals, Crh and corticosterone concentrations were attenuated at the end of rRes, but increased at the end of CVS treatments. Cold exposure increased mRNA levels of Crh, Trh, and serum concentration of thyrotropin in naïve, but not in rRes or CVS rats; corticosterone increased in all groups. Cold induced expression of thermogenic genes in BAT (Dio2 and Ucp1) in naïve but not in stressed rats; Adrb3 expression was differentially regulated.

CONCLUSION

Both types of chronic stress blunted HPT and BAT responses to cold. Long-term stress effects on noradrenergic and/or hormonal signaling are likely responsible for HPT dysfunction and not the type of chronic stressor.

摘要

目的

冷暴露会激活下丘脑-垂体-甲状腺(HPT)轴,而先前的急性应激或皮质酮给药会使这种反应减弱。慢性应激源会降低血清 T3 浓度和室旁核(PVN)中的促甲状腺素释放激素(Trh)表达,但对冷反应的影响尚不清楚;本研究在大鼠中进行,它们接受每日重复束缚(rRes),这会导致下丘脑-垂体-肾上腺(HPA)轴反应习惯化,或接受慢性可变应激(CVS),这会导致敏化和过度反应。

方法

雄性成年 Wistar 大鼠每天接受 30 分钟 rRes,或每天接受两次 CVS,共 15 天。在第 16 天,大鼠暴露于 5 或 21°C 1 小时。测量 HPT 和 HPA 轴活动以及棕色脂肪组织(BAT)冷反应的参数;通过 RT-PCR 测量 PVN 和 BAT 的基因表达;通过放射免疫分析或 ELISA 测量血清激素浓度。

结果

与未处理的动物相比,rRes 结束时 Crh 和皮质酮浓度降低,但 CVS 处理结束时增加。冷暴露增加了未处理大鼠的 Crh、Trh 和血清促甲状腺素浓度的 mRNA 水平,但不增加 rRes 或 CVS 大鼠的水平;所有组的皮质酮均增加。冷诱导了未处理大鼠 BAT 中产热基因(Dio2 和 Ucp1)的表达,但未处理大鼠中未诱导应激大鼠的表达;Adrb3 表达受到不同调节。

结论

两种类型的慢性应激都会使 HPT 和 BAT 对冷的反应减弱。长期应激对去甲肾上腺素能和/或激素信号的影响可能是 HPT 功能障碍的原因,而不是慢性应激源的类型。

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