Tjörnhammar M L, Lazaridis G, Bartfai T
Neurosci Lett. 1986 Jul 11;68(1):95-9. doi: 10.1016/0304-3940(86)90236-3.
The efflux of cyclic guanosine 3',5'-monophosphate (cGMP) was studied from rat cerebellar slices which were stimulated by L-glutamate (1 mM), or by depolarizing concentrations of K+ (60 mM) or by the nitroso compound, N-methyl-N'-nitro-N-nitrosoguanidine (MNNG). Via different mechanisms these agents stimulated cGMP synthesis producing several fold elevation of the cGMP content of the tissue slices. Simultaneously with the elevation of the intracellular (intra slice) concentrations of cGMP, a temperature-and time-dependent efflux of cGMP into the medium took place. This efflux was maximal at 5 min and could be inhibited by the known inhibitor of anion transport, probenecid, in a concentration-dependent manner. The results suggest the presence of an efflux system for cGMP, which may participate together with the well-characterized 3',5'-cyclic nucleotide phosphodiesterases in reduction of elevated cGMP levels.
研究了环鸟苷 3',5'-单磷酸(cGMP)从大鼠小脑切片中的流出情况,这些切片分别受到 L-谷氨酸(1 mM)、去极化浓度的 K⁺(60 mM)或亚硝基化合物 N-甲基-N'-硝基-N-亚硝基胍(MNNG)的刺激。通过不同机制,这些试剂刺激 cGMP 合成,使组织切片中的 cGMP 含量升高数倍。在细胞内(切片内)cGMP 浓度升高的同时,cGMP 以温度和时间依赖性方式流出到培养基中。这种流出在 5 分钟时达到最大值,并且可以被已知的阴离子转运抑制剂丙磺舒以浓度依赖性方式抑制。结果表明存在 cGMP 流出系统,其可能与已充分表征的 3',5'-环核苷酸磷酸二酯酶一起参与降低升高的 cGMP 水平。