Chritton S L, Dousa M K, Yaksh T L, Tyce G M
Department of Physiology, Mayo Clinic, Rochester, Minnesota 55905.
Am J Physiol. 1991 Mar;260(3 Pt 2):R589-99. doi: 10.1152/ajpregu.1991.260.3.R589.
The tissue content and overflow of norepinephrine (NE), epinephrine (Epi), dopamine (DA), Met-enkephalin (Met-Enk), and neuropeptide Y (NPY) from isolated, retrogradely perfused dog adrenal glands were studied. Under resting conditions, approximately 25% of the overflow of autocoids from the glands was Ca2+ dependent; the cholinergic antagonists hexamethonium and atropine had no effects on basal efflux. Stimulation with the nicotinic agonist 1,1-dimethyl-4-phenylpiperazinium iodide (DMPP; 3 or 50 microM) or with the muscarinic agonist pilocarpine (50 microM or 1 mM) evoked releases of autocoids. These releases were blocked or dramatically reduced by appropriate antagonists or by the removal of Ca2+ from the perfusate. Expressed as percentages of tissue stores, the rank order of overflow of autocoids was E approximately DA much greater than NE during resting conditions, DA much greater than E approximately NE during stimulation with 50 microM DMPP, and DA greater than Epi greater than NE during stimulation with 1 mM pilocarpine. These data are consistent with different mechanisms of release for the catecholamines, perhaps from different cell populations. The data support corelease of peptides and catecholamines, although clear pairing of autocoids could not be confirmed.
对从分离的、逆行灌注的犬肾上腺中去甲肾上腺素(NE)、肾上腺素(Epi)、多巴胺(DA)、甲硫氨酸脑啡肽(Met-Enk)和神经肽Y(NPY)的组织含量及溢出情况进行了研究。在静息状态下,来自腺体的类自体活性物质溢出约25%依赖于Ca2+;胆碱能拮抗剂六甲铵和阿托品对基础流出无影响。用烟碱激动剂碘化1,1-二甲基-4-苯基哌嗪(DMPP;3或50 μM)或毒蕈碱激动剂毛果芸香碱(50 μM或1 mM)刺激可诱发类自体活性物质释放。这些释放可被适当的拮抗剂阻断或显著减少,或通过从灌流液中去除Ca2+来实现。以组织储存量的百分比表示,类自体活性物质溢出的排序在静息状态下为E≈DA远大于NE,在用50 μM DMPP刺激时为DA远大于E≈NE,在用1 mM毛果芸香碱刺激时为DA大于Epi大于NE。这些数据与儿茶酚胺的不同释放机制一致,可能来自不同的细胞群体。这些数据支持肽类和儿茶酚胺的共同释放,尽管无法证实类自体活性物质之间有明确的配对关系。