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中枢促肾上腺皮质激素释放激素激活交感神经系统并降低免疫功能:老年大鼠反应性增强。

Central corticotropin-releasing hormone activates the sympathetic nervous system and reduces immune function: increased responsivity of the aged rat.

作者信息

Irwin M, Hauger R, Brown M

机构信息

Department of Psychiatry, University of California, San Diego 92161.

出版信息

Endocrinology. 1992 Sep;131(3):1047-53. doi: 10.1210/endo.131.3.1505449.

Abstract

CRH acts within the brain to activate the sympathetic nervous system and reduce cellular immune function. To determine the effects of age on CRH-induced elevations of sympathetic activity and suppression of immunity, we examined the responses of plasma catecholamines, neuropeptide-Y (NPY), corticosterone, and splenic natural killer (NK) activity after microinjection of rat CRH (200 pmol) into the lateral ventricle of aged (24-month-old) Fischer 344 (F344) rats compared to those in young (4-month-old) F344 rats. Basal concentrations of plasma norepinephrine and NPY were higher in the aged than in the young animals. In addition, CRH produced a greater elevation of plasma levels of catecholamines and NPY, which persisted for a longer period of time in the aged rats compared to responses in the young animals. Splenic NK activity showed an age-related decrement at baseline, and CRH induced a further significant (P less than 0.01) reduction of lytic activity in the aged rats, but did not alter cytotoxicity in the young rats. Corticosterone basal levels and responses were similar in the aged and young rats. These results show an age-related increase in autonomic outflow and suppression of NK activity after central CRH administration. In aged animals, the central nervous system may have a role in abnormal regulation of sympathetic activity and suppression of natural cytotoxicity in vivo.

摘要

促肾上腺皮质激素释放激素(CRH)在脑内发挥作用,激活交感神经系统并降低细胞免疫功能。为了确定年龄对CRH诱导的交感神经活动增强和免疫抑制的影响,我们将大鼠CRH(200皮摩尔)微量注射到老(24月龄)的Fischer 344(F344)大鼠侧脑室后,检测了血浆儿茶酚胺、神经肽Y(NPY)、皮质酮和脾脏自然杀伤(NK)活性的反应,并与年轻(4月龄)F344大鼠进行比较。老年动物血浆去甲肾上腺素和NPY的基础浓度高于年轻动物。此外,与年轻动物的反应相比,CRH使老年大鼠血浆儿茶酚胺和NPY水平升高幅度更大,且持续时间更长。脾脏NK活性在基线时显示出与年龄相关的下降,CRH诱导老年大鼠的裂解活性进一步显著(P小于0.01)降低,但未改变年轻大鼠的细胞毒性。老年和年轻大鼠的皮质酮基础水平及反应相似。这些结果表明,中枢给予CRH后,自主神经输出与年龄相关增加,NK活性受到抑制。在老年动物中,中枢神经系统可能在体内交感神经活动的异常调节和自然细胞毒性的抑制中起作用。

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