Archives of Pharmacal Research
- Volume 14 Issue 1
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- Pages.55-67
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- 1991
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- 0253-6269(pISSN)
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- 1976-3786(eISSN)
Studies on Secretion of Catecholamine Evoked by Caffeine from the Isolated Perfused Rat Adrenal Gland
- Lim, Dong-Yoon (College of Pharmacy, Chosun University) ;
- Lee, Jang-Hee (College of Pharmacy, Chosun University) ;
- Kim, Won-Shik (College of Pharmacy, Chosun University) ;
- Kim, Soo-Bok (College of Pharmacy, Chosun University) ;
- Lee, Eun-Hwa (College of Pharmacy, Chosun University) ;
- Lee, Byeong-Joo (College of Medicine, Chosun University) ;
- Ko, Suk-Tai (College of Medicine, Chosun University)
- Published : 1991.03.01
Abstract
The influence of caffeine on secretion of catecholamines (CA) was examined in the isolated perfused rat adrenal gland. Caffeine (0.3 mM) perfused into an adrenal vein of the gland produced a marked increase in secretion of CA. This secretory effect of CA evoked by perfusion of caffeine for one minute was considerably prolonged, lasting for more than 90 minutes. The tachyphylaxis to releasing effect of CA induced by caffeine was observed by repeated perfusion of this drug. The caffeine-evoked CA secretion was markedly inhibited by pretreatment with ouabain, trifluoperazine, TMB-8 and perfusion with calcium-free Krebs solution containing 5 mM EGTA, but was not affected by perfusion of calcium-free Krebs solution without other addition. CA secretion evoked by caffeine was not reduced significantly by pretreatment with chlorisondamine but after the first collection of perfusate for 3 min was clearly inhibited. Interestingly, the caffeine-evoked CA secretion was considerably potentiated by pretreatment with atropine or pirenzepine, but after the first collection for 3 min it was markedly decreased. These experimental results suggest that caffeine causes a marked increase in secretion of CA from the isolated perfused rat adrenal gland by an extracellular calcium-independent exocytotic mechanism. The secretory effect of caffeine may be mainly due to mobilization of calcium from an intracellular calcium pool in the rat chromaffin cells and partly due to stimulation of both muscarinic and nicotinic receptors.