Tsubota Yuji, Owada-Makabe Kyoko, Yukawa Kazunori, Maeda Masanobu
Department of Physiology, Wakayama Medical University School of Medicine, Kimiidera 811-1, Wakayama City, Wakayama 641-8509, Japan.
Neuroreport. 2005 Feb 8;16(2):163-6. doi: 10.1097/00001756-200502080-00019.
Ghrelin is a gut-brain peptide and its endocrine activities are mediated by GH secretagogue receptor (GHSR)-1a. Des-acyl ghrelin does not activate GHSR-1a and is devoid of endocrine activities. While the microinjection of ghrelin into rat nucleus tractus solitarii (NTS) elicited hypotensive effects, this was not the case upon injection into GHSR-expressing rostral ventrolateral medulla or caudal ventrolateral medulla. To make clear the reason of the discrepancy between receptor distribution and neuronal responses, we examined the cardiovascular response of rats microinjected with des-acyl ghrelin into NTS. Intra-NTS injection of des-acyl ghrelin significantly reduced mean arterial pressure and heart rate. The hypotensive and bradycardic activity evoked by des-acyl ghrelin was not significantly different from that of native ghrelin. These results suggest that des-acyl ghrelin contribute to the regulation of cardiovascular control and that a receptor other than GHSR-1a exists in NTS.
胃饥饿素是一种脑肠肽,其内分泌活性由生长激素促分泌素受体(GHSR)-1a介导。去酰基胃饥饿素不激活GHSR-1a,且缺乏内分泌活性。虽然向大鼠孤束核(NTS)微量注射胃饥饿素会引起降压作用,但向表达GHSR的延髓头端腹外侧区或延髓尾端腹外侧区注射时则不会出现这种情况。为了弄清楚受体分布与神经元反应之间差异的原因,我们检测了向NTS微量注射去酰基胃饥饿素的大鼠的心血管反应。向NTS内注射去酰基胃饥饿素可显著降低平均动脉压和心率。去酰基胃饥饿素诱发的降压和心动过缓活性与天然胃饥饿素的并无显著差异。这些结果表明,去酰基胃饥饿素有助于心血管控制的调节,且NTS中存在除GHSR-1a之外的受体。