Lopez G A, Khalighi K, Ebneshahidi A, Gonzales E, Jaramillo S, Rivas S
Prostaglandins Leukot Med. 1985 Aug;19(2):105-13. doi: 10.1016/0262-1746(85)90075-7.
Using a renal cortical slice system from sodium loaded (SL) or sodium deficient (SD) rats, this study investigated whether the effect of prostaglandin E2 (PGE2) on renin release (RR) is mediated by tissue cyclic AMP content (TcAMPc) changes, and if it can be modified by dietary sodium manipulation. At 10(-5) M, PGE2 significantly stimulated RR and TcAMPc in both SL and SD groups of slices. PGE2 doses of 10(-9) M and 10(-7) M were ineffective, although RR, but not TcAMPc, was significantly greater in the SD group in response to 10(-7) M PGE2 than RR in the SL group. Addition of the phosphodiesterase inhibitor theophylline (10(-4) M) together with the same three PGE2 doses maintained the stimulatory effect of 10(-5)M PGE2 alone on RR and TcAMPc in both groups of slices, and reversed the effect of 10(-7) M PGE2 alone on RR and TcAMPc in the SD group of slices only. Added by itself, theophylline was ineffective. These data indicate that: PGE2 can stimulate RR by a direct effect on the juxtaglomerular cells; the RR responses to PGE2 and theophylline administration are enhanced in the SD state; and the possibility of cAMP mediation of the effect of PGE2 on RR is discussed.
本研究利用来自钠负荷(SL)或缺钠(SD)大鼠的肾皮质切片系统,探讨前列腺素E2(PGE2)对肾素释放(RR)的影响是否由组织环磷酸腺苷含量(TcAMPc)变化介导,以及其是否可被饮食钠操作所改变。在10^(-5) M浓度下,PGE2显著刺激了SL组和SD组切片中的RR和TcAMPc。10^(-9) M和10^(-7) M剂量的PGE2无效,尽管在SD组中,10^(-7) M PGE2刺激后的RR显著高于SL组,但此时两组的TcAMPc并无显著差异。同时添加磷酸二酯酶抑制剂茶碱(10^(-4) M)和上述三种PGE2剂量,可维持10^(-5)M PGE2单独对两组切片RR和TcAMPc的刺激作用,并且仅逆转了10^(-7) M PGE2单独对SD组切片RR和TcAMPc的作用。单独添加茶碱则无效。这些数据表明:PGE2可通过直接作用于球旁细胞来刺激RR;在SD状态下,RR对PGE2和茶碱给药的反应增强;并对PGE2对RR的作用通过cAMP介导的可能性进行了讨论。