Yoshimura R, Yanagihara N, Terao T, Minami K, Abe K, Izumi F
Department of Psychiatry, University of Occupational and Environmental Health, School of Medicine, Fukuoka, Japan.
Naunyn Schmiedebergs Arch Pharmacol. 1995 Sep;352(3):297-303. doi: 10.1007/BF00168560.
The effects of carbamazepine (CBZ) on 22Na+ influx, 45Ca2- influx, catecholamine secretion and cyclic GMP production were examined in cultured bovine adrenal medullary cells. 1) CBZ (40-120 mumol/l) inhibited 22Na+ influx evoked by carbachol in a concentration-dependent manner. CBZ inhibited carbachol-evoked 45Ca2- influx and catecholamine secretion at concentrations similar to those which suppressed 22Na+ influx. 2) CBZ (4-120 mumol/l) inhibited veratridine-induced 22Na+ influx, 45Ca2+ influx and catecholamine secretion. 3) CBZ (12 or 40-120 mumol/l) suppressed 56 mmol/l K(+)-evoked 45Ca2+ influx and catecholamine secretion, respectively. 4) Combination of CBZ with nitrendipine or omega-agatoxin-IVA produced further inhibition of 56 mmol/l K(+)-evoked 45Ca2+ influx and catecholamine secretion, compared to the effect of CBZ alone, whereas CBZ plus omega-conotoxin-GVIA did not produce any further inhibition. 5) CBZ (40 mumol/l) attenuated the production of cyclic GMP caused by muscarine. These results suggest that CBZ at therapeutic concentrations (16-48 mumol/l; 4-12 micrograms/ml) inhibits catecholamine secretion by interfering with nicotinic acetylcholine receptor-associated ion channels, voltage-dependent Na+ channels and N-type voltage-dependent Ca2+ channels, and may have an antimuscarinic effect in adrenal medullary cells.
在培养的牛肾上腺髓质细胞中研究了卡马西平(CBZ)对22Na+内流、45Ca2-内流、儿茶酚胺分泌和环鸟苷酸生成的影响。1)CBZ(40 - 120μmol/l)以浓度依赖性方式抑制卡巴胆碱诱发的22Na+内流。CBZ在抑制22Na+内流的相似浓度下,抑制卡巴胆碱诱发的45Ca2-内流和儿茶酚胺分泌。2)CBZ(4 - 120μmol/l)抑制藜芦碱诱导的22Na+内流、45Ca2+内流和儿茶酚胺分泌。3)CBZ(12或40 - 120μmol/l)分别抑制56mmol/l K(+)诱发的45Ca2+内流和儿茶酚胺分泌。4)与单独使用CBZ的效果相比,CBZ与尼群地平或ω-芋螺毒素-IVA联合使用对56mmol/l K(+)诱发的45Ca2+内流和儿茶酚胺分泌产生进一步抑制,而CBZ加ω-芋螺毒素-GVIA未产生任何进一步抑制。5)CBZ(40μmol/l)减弱了毒蕈碱引起的环鸟苷酸生成。这些结果表明,治疗浓度(16 - 48μmol/l;4 - 12μg/ml)的CBZ通过干扰烟碱型乙酰胆碱受体相关离子通道、电压依赖性Na+通道和N型电压依赖性Ca2+通道来抑制儿茶酚胺分泌,并且可能在肾上腺髓质细胞中具有抗毒蕈碱作用。