Tsuda K, Tsuda S, Goldstein M, Nishio I, Masuyama Y
Division of Cardiology, Wakayama Medical College, Japan.
Hypertension. 1992 Jun;19(6 Pt 2):639-42. doi: 10.1161/01.hyp.19.6.639.
In the present study, we examined the regulatory mechanisms of calcitonin gene-related peptide on norepinephrine release in rat hypothalamus. Calcitonin gene-related peptide inhibited the stimulation-evoked norepinephrine release from hypothalamic slices of Sprague-Dawley rats in a dose-dependent manner, although the peptide did not affect basal release of norepinephrine. The blockade of the alpha 2-adrenergic receptors by RX 781094 failed to modulate the inhibitory effects of calcitonin gene-related peptide on norepinephrine release. Pretreatment of slices with islet activating protein, a toxin that interferes with the coupling of the inhibitory receptors to adenylate cyclase, did not affect the suppression of norepinephrine release by calcitonin gene-related peptide. However, Bay K 8644, a dihydropyridine-sensitive calcium channel agonist, significantly reversed the inhibitory effects of calcitonin gene-related peptide on norepinephrine release. These results show that calcitonin gene-related peptide might inhibit norepinephrine release in rat hypothalamus, partially mediated by interactions with dihydropyridine-sensitive Ca2+ channels but not by interactions with presynaptic alpha 2-adrenergic receptors and inhibitory guanosine triphosphate binding proteins. Furthermore, the finding suggests the possible involvement of calcitonin gene-related peptide in the regulation of sympathetic nervous activity in the central nervous system.
在本研究中,我们检测了降钙素基因相关肽对大鼠下丘脑去甲肾上腺素释放的调节机制。降钙素基因相关肽以剂量依赖的方式抑制了刺激诱发的来自Sprague-Dawley大鼠下丘脑切片的去甲肾上腺素释放,尽管该肽并不影响去甲肾上腺素的基础释放。RX 781094对α2-肾上腺素能受体的阻断未能调节降钙素基因相关肽对去甲肾上腺素释放的抑制作用。用胰岛激活蛋白(一种干扰抑制性受体与腺苷酸环化酶偶联的毒素)对切片进行预处理,并不影响降钙素基因相关肽对去甲肾上腺素释放的抑制作用。然而,二氢吡啶敏感性钙通道激动剂Bay K 8644显著逆转了降钙素基因相关肽对去甲肾上腺素释放的抑制作用。这些结果表明,降钙素基因相关肽可能抑制大鼠下丘脑的去甲肾上腺素释放,部分是通过与二氢吡啶敏感性Ca2+通道相互作用介导的,而非通过与突触前α2-肾上腺素能受体和抑制性鸟苷三磷酸结合蛋白相互作用介导。此外,这一发现提示降钙素基因相关肽可能参与中枢神经系统交感神经活动的调节。