Kitayama S, Morita K, Dohi T, Tsujimoto A
Naunyn Schmiedebergs Arch Pharmacol. 1984 Jun;326(2):106-10. doi: 10.1007/BF00517305.
The effect of gamma-aminobutyric acid (GABA) on catecholamine (CA) release from adrenal medulla was investigated. GABA and GABA agonists, 3-amino-1-propane-sulfonic acid and imidazole-4-acetic acid caused CA release from isolated perfused dog adrenals in a dose-dependent manner, and no tachyphylaxis to GABA was observed. CA release elicited by GABA was antagonized by bicuculline and picrotoxin. This antagonism was specific for GABA- and GABA agonist-induced responses, response to acetylcholine being unaffected. Pretreatment with atropine plus hexamethonium did not affect the response to GABA. GABA-induced CA release was abolished by the removal of Ca2+ from perfusion medium, but not by the removal of Na+ or Cl-. Verapamil, CoCl2 and dibucaine blocked the effect of GABA. A Na+ channel blocker, tetrodotoxin did not reduce GABA-evoked CA release. These results suggest that GABA may interact with its receptor to evoke CA release from adrenal medulla in a fashion of Ca2+-dependence and independence on external Na+ or Cl-.
研究了γ-氨基丁酸(GABA)对肾上腺髓质儿茶酚胺(CA)释放的影响。GABA及其激动剂3-氨基-1-丙烷磺酸和咪唑-4-乙酸以剂量依赖的方式引起离体灌注犬肾上腺释放CA,且未观察到对GABA的快速耐受性。GABA引起的CA释放被荷包牡丹碱和印防己毒素拮抗。这种拮抗作用对GABA和GABA激动剂诱导的反应具有特异性,对乙酰胆碱的反应不受影响。用阿托品加六甲铵预处理不影响对GABA的反应。从灌注培养基中去除Ca2+可消除GABA诱导的CA释放,但去除Na+或Cl-则不能。维拉帕米、氯化钴和丁卡因可阻断GABA的作用。一种Na+通道阻滞剂河豚毒素并未减少GABA诱发的CA释放。这些结果表明,GABA可能与其受体相互作用,以一种依赖Ca2+且不依赖外部Na+或Cl-的方式引起肾上腺髓质释放CA。