Iitake K, Share L, Brooks D P, Crofton J T, Ouchi Y
Department of Physiology and Biophysics, University of Tennessee-Memphis 38163.
Exp Brain Res. 1989;75(1):47-52. doi: 10.1007/BF00248529.
There is considerable evidence to suggest that there is a cholinergic link in the neural control of vasopressin release, but the precise role for this link has not been adequately demonstrated in the intact animal. We have, therefore, examined in conscious unrestrained rats the effects of central cholinergic blockade on the stimulation of vasopressin release by increased plasma osmotality (iv infusion of 2.5 M NaCl at 0.1 mg/kg body weight.min for 30 min) and by decreased blood volume (2 successive hemorrhages of 10% of blood volume each). The vasopressin responses to these stimuli were unaffected by either intracerebroventricular (icv) atropine (10 micrograms; muscarinic blockade) or icv hexamethonium (10 micrograms; nicotinic blockade) in doses which block the vasopressin responses to icv cholinergic agonists. The implications of these findings are discussed.
有大量证据表明,在血管加压素释放的神经控制中存在胆碱能联系,但在完整动物中,这一联系的确切作用尚未得到充分证实。因此,我们在清醒不受约束的大鼠中,研究了中枢胆碱能阻断对因血浆渗透压升高(以0.1mg/kg体重·分钟的速度静脉输注2.5M NaCl 30分钟)和血容量减少(连续两次放血,每次放血量为血容量的10%)而刺激血管加压素释放的影响。在能阻断血管加压素对脑室内胆碱能激动剂反应的剂量下,脑室内注射阿托品(10微克;毒蕈碱阻断)或六甲铵(10微克;烟碱阻断)对这些刺激的血管加压素反应均无影响。文中讨论了这些发现的意义。