Vernejoul Fabienne, Damase-Michel Christine, Montastruc Jean-Louis, Tran Marie-Antoinette
Laboratoire de Pharmacologie Médicale et Clinique, INSERM U317, Faculté de Médecine, 37 allées Jules Guesde, 31073 Toulouse Cedex, France.
Eur J Pharmacol. 2002 May 31;444(3):197-202. doi: 10.1016/s0014-2999(02)01646-1.
The study investigated the effects of dopamine D1-like receptor stimulation on the autonomic nervous system. Fenoldopam (20 microg/kg) was injected i.v. in conscious sinoaortic denervated dogs, that is, surgically deprived of baroreflex pathways. In barodenervated dogs, fenoldopam (20 microg/kg) induced arterial hypotension as well as bradycardia and reduced noradrenaline plasma levels. Pentolinium (0.1 mg/kg i.v.), used to induce partial blockade of nicotinic ganglionic receptors, suppressed the fenoldopam-induced decrease in sympathetic tone, suggesting a ganglionic location for the dopamine D1-like receptor. Moreover, the inability of fenoldopam to reduce the nicotine-induced increase in sympathetic tone suggests that a postsynaptic ganglionic location can be excluded for the dopamine D1-like receptor. The results of these "in vivo" experiments strongly suggest a presynaptic location for the ganglionic dopamine D1-like receptor, stimulation of which results in a reduction of sympathetic tone.
该研究调查了多巴胺D1样受体刺激对自主神经系统的影响。将非诺多泮(20微克/千克)静脉注射到清醒的去窦弓神经犬体内,即通过手术剥夺压力反射通路的犬。在去压力神经犬中,非诺多泮(20微克/千克)引起动脉低血压以及心动过缓,并降低了血浆去甲肾上腺素水平。潘托铵(0.1毫克/千克静脉注射)用于诱导烟碱型神经节受体部分阻断,抑制了非诺多泮引起的交感神经张力降低,提示多巴胺D1样受体位于神经节。此外,非诺多泮无法降低尼古丁引起的交感神经张力增加,提示多巴胺D1样受体可排除位于神经节后突触位置。这些“体内”实验结果强烈提示神经节多巴胺D1样受体位于突触前,刺激该受体可导致交感神经张力降低。