Tsutsui M, Yanagihara N, Minami K, Kobayashi H, Nakashima Y, Kuroiwa A, Izumi F
Department of Pharmacology, University of Occupational and Environmental Health, School of Medicine, Fukuoka, Japan.
J Pharmacol Exp Ther. 1994 Feb;268(2):584-9.
We examined the effects of C-type natriuretic peptide (CNP) on cyclic GMP production and catecholamine synthesis in cultured bovine adrenal medullary cells. 1) CNP increased intracellular cyclic GMP content in a concentration-dependent manner (10-1000 nM). 2) The cyclic GMP production induced by 1 microM CNP reached a 200-fold increase, and the effect of CNP was most potent among the natriuretic peptide family. 3) The CNP-induced cyclic GMP production was attenuated by endothelin (1 microM) and angiotensin II (0.1-1 microM). 4) When the cells were cultured with hypertonic NaCl medium, the CNP-induced cyclic GMP production was potentiated in a time (1-4 days)- and concentration (25-100 mM)-dependent manner. 5) CNP stimulated the synthesis of 14C-labeled catecholamines from [14C] tyrosine but not from [14C] dopa. The stimulatory effect of CNP on the 14C-labeled catecholamine synthesis was observed at the concentrations of 100 to 100 nM. 6) 8-Bromo cyclic GMP, a membrane-permeable cyclic GMP analog, and sodium nitroprusside, an activator of soluble guanylate cyclase, also stimulated the synthesis of 14C-labeled catecholamines from [14C]tyrosine, whereas C-ANF, a specific ligand for the ANP-C (clearance) receptor that does not increase cyclic GMP content, failed to stimulate the synthesis of 14C-labeled catecholamines. 7) CNP (1 microM) as well as 8-bromo cyclic GMP and sodium nitroprusside increased the activity of tyrosine hydroxylase in the cells. These results suggest that in the adrenal medulla, CNP is a potent agonist for cyclic GMP production, which is modulated by endothelin, angiotensin II and the hypertonic NaCl condition.(ABSTRACT TRUNCATED AT 250 WORDS)
我们研究了C型利钠肽(CNP)对培养的牛肾上腺髓质细胞中环磷酸鸟苷(cGMP)生成及儿茶酚胺合成的影响。1)CNP以浓度依赖性方式(10 - 1000 nM)增加细胞内cGMP含量。2)1 microM CNP诱导的cGMP生成增加了200倍,且CNP在利钠肽家族中作用最为显著。3)内皮素(1 microM)和血管紧张素II(0.1 - 1 microM)可减弱CNP诱导的cGMP生成。4)当细胞在高渗NaCl培养基中培养时,CNP诱导的cGMP生成以时间(1 - 4天)和浓度(25 - 100 mM)依赖性方式增强。5)CNP刺激从[14C]酪氨酸而非[14C]多巴合成14C标记的儿茶酚胺。在100至100 nM浓度下可观察到CNP对14C标记的儿茶酚胺合成的刺激作用。6)8 - 溴环磷酸鸟苷(一种可透过细胞膜的环磷酸鸟苷类似物)和硝普钠(可溶性鸟苷酸环化酶激活剂)也刺激从[14C]酪氨酸合成14C标记的儿茶酚胺,而C - ANF(ANP - C(清除)受体的特异性配体,不增加cGMP含量)未能刺激14C标记的儿茶酚胺合成。7)CNP(1 microM)以及8 - 溴环磷酸鸟苷和硝普钠增加细胞中酪氨酸羟化酶的活性。这些结果表明,在肾上腺髓质中,CNP是cGMP生成的强效激动剂,其受内皮素、血管紧张素II和高渗NaCl条件的调节。(摘要截短为250字)