Gintonin facilitates catecholamine secretion from the perfused adrenal medulla

被引:2
|
作者
Na, Seung-Yeol [1 ]
Kim, Ki-Hwan [2 ]
Choi, Mi-Sung [3 ]
Ha, Kang-Su [4 ]
Lim, Dong-Yoon [5 ]
机构
[1] Konkuk Univ, Dept Physiol, Coll Vet Med, Seoul 05029, South Korea
[2] Boramae Seoul Natl Univ, Sch Med, Dept Internal Med, Seoul 07061, South Korea
[3] Dongshin Univ, Dept Leisure & Sport, Coll Publ Hlth & Welf, Naju 58245, South Korea
[4] Chosun Univ, Coll Med, Dept Psychiat, Gwangju 61452, South Korea
[5] Chosun Univ, Coll Med, Dept Pharmacol, Gwangju 61452, South Korea
来源
KOREAN JOURNAL OF PHYSIOLOGY & PHARMACOLOGY | 2016年 / 20卷 / 06期
关键词
Adrenal medulla; Catecholamine secretion; Gintonin; Hypertensive component; LPA receptor; LYSOPHOSPHATIDIC ACID RECEPTORS; ENDOTHELIUM-DEPENDENT RELAXATION; BOVINE CHROMAFFIN CELLS; KOREA RED GINSENG; BLOOD-PRESSURE; INTRACELLULAR CALCIUM; MUSCARINIC RECEPTORS; RAT AORTA; NEUROTRANSMITTER RELEASE; ESSENTIAL-HYPERTENSION;
D O I
10.4196/kjpp.2016.20.6.629
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The present study was designed to investigate the characteristics of gintonin, one of components isolated from Korean Ginseng on secretion of catecholamines (CA) from the isolated perfused model of rat adrenal gland and to clarify its mechanism of action. Gintonin (1 to 30 mu g/ml), perfused into an adrenal vein, markedly increased the CA secretion from the perfused rat adrenal medulla in a dose-dependent fashion. The gintonin-evoked CA secretion was greatly inhibited in the presence of chlorisondamine (1 mu M, an autonomic ganglionic bloker), pirenzepine (2 mu M a muscarinic M-1 receptor antagonist), Ki14625 (10 mu M, an LPA(1/3) receptor antagonist), amiloride (1 mM, an inhibitor of Na+/Ca2+ exchanger), a nicardipine (1 mu M, a voltage-dependent Ca2+ channel blocker), TMB-8 (1 mu M, an intracellular Ca2+ antagonist), and perfusion of Ca2+-free Krebs solution with 5mM EGTA (a Ca2+ chelater), while was not affected by sodium nitroprusside (100 mu M, a nitrosovasodialtor). Interestingly, LPA (0.3 similar to 3 mu M, an LPA receptor agonist) also dose-dependently enhanced the CA secretion from the adrenal medulla, but this facilitatory effect of LPA was greatly inhibited in the presence of Ki 14625 (10 mu M). Moreover, acetylcholine (AC)-evoked CA secretion was greatly potentiated during the perfusion of gintonin (3 mu g/ml). Taken together, these results demonstrate the first evidence that gintonin increases the CA secretion from the perfused rat adrenal medulla in a dose -dependent fashion. This facilitatory effect of gintonin seems to be associated with activation of LPA- and cholinergic-receptors, which are relevant to the cytoplasmic Ca2+ increase by stimulation of the Ca2+ influx as well as by the inhibition of Ca2+ uptake into the cytoplasmic Ca2+ stores, without the increased nitric oxide (NO). Based on these results, it is thought that gintonin, one of ginseng components, can elevate the CA secretion from adrenal medulla by regulating the Ca2+ mobilization for exocytosis, suggesting facilitation of cardiovascular system. Also, these findings show that gintonin might be at least one of ginseng-induced hypertensive components.
引用
收藏
页码:629 / 639
页数:11
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