Yanagihara N, Yokota K, Wada A, Izumi F
Department of Pharmacology, University of Occupational and Environmental Health, School of Medicine, Fukuoka, Japan.
J Neurochem. 1987 Dec;49(6):1740-6. doi: 10.1111/j.1471-4159.1987.tb02431.x.
Incubation of cultured bovine adrenal medullary cells in Na+-free sucrose medium or in Na+-free Cs+ medium enhanced the synthesis of 14C-catecholamines from [14C]tyrosine about two- to threefold or sixfold, respectively. The increment of 14C-catecholamine synthesis produced by Na+-free medium was partially dependent on the presence of Ca2+ in the medium. Dibutyryl cyclic AMP also stimulated the synthesis of 14C-catecholamines in adrenal medullary cells, and the effects of Na+ removal and dibutyryl cyclic AMP (5 mM) on the synthesis were almost additive. The intracellular pH measured by using a weak acid 5,5-dimethyloxazolidine-2,4-dione was 7.14 in control cells and when Na+ was replaced by sucrose or Cs+, it shifted down to 6.56 or 5.66, respectively. The fall in intracellular pH and the stimulation of 14C-catecholamine synthesis were similarly dependent on the concentration of Na+ in the medium. The optimal pH of soluble tyrosine hydroxylase was 5.5-6.0 both in control cells and in cells incubated in Na+-free medium. These results suggest that removal of extracellular Na+ increases the synthesis of catecholamines, at least in part, by shifting the intracellular pH toward the optimal pH of tyrosine hydroxylase.
将培养的牛肾上腺髓质细胞置于无钠蔗糖培养基或无钠铯培养基中培养时,[14C]酪氨酸合成14C - 儿茶酚胺的量分别增加了约2至3倍或6倍。无钠培养基引起的14C - 儿茶酚胺合成增加部分依赖于培养基中Ca2+的存在。二丁酰环磷腺苷也刺激肾上腺髓质细胞中14C - 儿茶酚胺的合成,去除Na+和二丁酰环磷腺苷(5 mM)对合成的影响几乎是相加的。使用弱酸5,5 - 二甲基恶唑烷 - 2,4 - 二酮测量的对照细胞内pH值为7.14,当用蔗糖或铯取代Na+时,分别降至6.56或5.66。细胞内pH值的下降和14C - 儿茶酚胺合成的刺激同样依赖于培养基中Na+的浓度。对照细胞和在无钠培养基中培养的细胞中,可溶性酪氨酸羟化酶的最佳pH值均为5.5 - 6.0。这些结果表明,去除细胞外Na+至少部分地通过使细胞内pH值向酪氨酸羟化酶的最佳pH值移动来增加儿茶酚胺的合成。