Schulz C, Christodulopulu E, Bock A, Kretz M, Beyer J, Lehnert H
Department of Endocrinology and Metabolism, University Hospital of Magdeburg, Germany.
Neuropsychobiology. 1994;30(4):178-84. doi: 10.1159/000119158.
The neuropeptides thyrotropin-releasing hormone (TRH) and corticotropin-releasing hormone (CRH) have been found to be potent stimulators of the autonomic nervous system in both experimental animals and humans. We studied the effects of different doses of CRH and TRH given intracerebroventricularly in the urethane-anesthetized rat and a single dose of CRH in the chloral hydrate-anesthetized rat to elucidate the effects of these peptides in the unconscious state. All TRH doses studied enhanced blood pressure and noradrenaline and adrenaline secretion. Surprisingly, there were no blood pressure increases following administration of 0.4, 1.3 and 1.7 nmol CRH. In general, there was a tendency for blood pressure to decrease with the largest drop observed after 1.7 nmol CRH. Our data suggest that only TRH clearly augments blood pressure and catecholamine secretion in the anesthetized animal, while CRH does not exert major effects under the two anesthetic conditions employed.
已发现神经肽促甲状腺激素释放激素(TRH)和促肾上腺皮质激素释放激素(CRH)在实验动物和人类中都是自主神经系统的强效刺激物。我们研究了在氨基甲酸乙酯麻醉的大鼠中脑室内给予不同剂量的CRH和TRH以及在水合氯醛麻醉的大鼠中给予单剂量CRH的效果,以阐明这些肽在无意识状态下的作用。所研究的所有TRH剂量均提高了血压以及去甲肾上腺素和肾上腺素的分泌。令人惊讶的是,给予0.4、1.3和1.7 nmol CRH后血压并未升高。总体而言,血压有下降的趋势,在给予1.7 nmol CRH后观察到最大降幅。我们的数据表明,在麻醉动物中只有TRH能明显提高血压和儿茶酚胺分泌,而在所用的两种麻醉条件下CRH未发挥主要作用。