Godinho Rosely Oliveira, Costa Valter Luiz
Department of Pharmacology (INFAR), Universidade Federal de São Paulo-Escola Paulista de Medicina, Rua Três de Maio, 100, São Paulo, SP, Brazil-04044-020.
Br J Pharmacol. 2003 Mar;138(5):995-1003. doi: 10.1038/sj.bjp.0705130.
(1) This report analyses the intracellular and extracellular accumulation of cyclic AMP in primary rat skeletal muscle cultures, after direct and receptor-dependent stimulation of adenylyl cyclase (AC). (2) Isoprenaline, calcitonin gene-related peptide (CGRP) and forskolin induced a transient increase in the intracellular cyclic AMP that peaked 5 min after onset stimulation. (3) Under stimulation with isoprenaline or CGRP, the intracellular cyclic AMP initial rise was followed by an exponential decline, reaching 46 and 52% of peak levels in 10 min, respectively. (4) Conversely, the forskolin-dependent accumulation of intracellular cyclic AMP decreased slowly and linearly, reaching 49% of the peak level in 30 min. (5) The loss of intracellular cyclic AMP from peak levels, induced by direct or receptor-induced activation of AC, was followed by an increase in the extracellular cyclic AMP. (6) This effect was independent on PDEs, since it was obtained in the presence of 3-isobutyl-1-methylxanthine (IBMX). (7) Besides, in isoprenaline treated cells, the beta-adrenoceptor antagonist propranolol reduced both intra- and extracellular accumulation of cyclic AMP, whereas the organic anion transporter inhibitor probenecid reduced exclusively the extracellular accumulation. (8) Together our data show that direct or receptor-dependent activation of skeletal muscle AC results in a transient increase in the intracellular cyclic AMP, despite the continuous presence of the stimulus. The temporal declining of intracellular cyclic AMP was not dependent on the cyclic AMP breakdown but associated to the efflux of cyclic nucleotide to the extracellular compartment, by an active transport since it was prevented by probenecid.
(1) 本报告分析了原代大鼠骨骼肌培养物中,在直接刺激和受体依赖性刺激腺苷酸环化酶(AC)后,环磷酸腺苷(cAMP)在细胞内和细胞外的积累情况。(2) 异丙肾上腺素、降钙素基因相关肽(CGRP)和福斯高林可诱导细胞内cAMP短暂增加,在刺激开始后5分钟达到峰值。(3) 在异丙肾上腺素或CGRP刺激下,细胞内cAMP的初始升高之后是指数下降分别在10分钟内降至峰值水平的46%和52%。(4) 相反,福斯高林依赖性的细胞内cAMP积累下降缓慢且呈线性,在30分钟内降至峰值水平的49%。(5) 由AC的直接激活或受体诱导激活引起的细胞内cAMP从峰值水平的下降,随后是细胞外cAMP的增加。(6) 这种效应不依赖于磷酸二酯酶(PDEs),因为在存在3 - 异丁基 - 1 - 甲基黄嘌呤(IBMX)的情况下也能观察到。(7) 此外,在异丙肾上腺素处理的细胞中,β - 肾上腺素能受体拮抗剂普萘洛尔降低了细胞内和细胞外cAMP的积累,而有机阴离子转运体抑制剂丙磺舒仅降低了细胞外积累。(8) 我们的数据共同表明,尽管刺激持续存在,但骨骼肌AC的直接激活或受体依赖性激活会导致细胞内cAMP短暂增加。细胞内cAMP的时间性下降不依赖于cAMP的分解,而是与环核苷酸通过主动转运外流到细胞外区室有关,因为丙磺舒可阻止这种外流。