Franklin S O, Zhu Y S, Yoburn B C, Inturrisi C E
Department of Pharmacology, Cornell University Medical College, New York, NY 10021.
Mol Pharmacol. 1991 Oct;40(4):515-22.
Transsynaptic neurogenic activity and reserpine are two signals that cause the proenkephalin (Penk) gene to alter the levels of preproenkephalin (PPenk) mRNA and enkephalin-containing (EC) peptides. In the Syrian hamster adrenal, but not in rat adrenal, both of these signals appear to be positive activators of Penk gene expression. The separate and combined effects of reserpine and denervation on EC peptides and catecholamine systems were investigated in the adrenal of the hamster, a species with relatively high medullary PPenk mRNA and EC peptide levels. Unilateral adrenal denervation resulted in a rapid decrease in PPenk mRNA levels of 54% after 2 days, and by 11 days 90% of Penk mRNA had disappeared. After 4 days both EC peptide and PPenk mRNA levels fell in parallel, whereas total RNA and soluble protein levels were unchanged. Denervation had no effect on TH mRNA levels until 8 days after surgery, and after 11 days both TH mRNA and catecholamine levels had decreased by 35-45%. Reserpine produced a dose- and time-dependent depletion of EC peptides and catecholamines. One day after 5 mg/kg reserpine (given subcutaneously on each of 2 consecutive days), EC peptides were reduced by 80%, norepinephrine by 79%, and epinphrine by greater than 95%. By 4 days after treatment, EC peptides and catecholamines slightly exceeded or had returned to control (concurrent vehicle treatment) values. PPenk mRNA levels, as measured by solution hybridization, were doubled (206 +/- 17%, mean +/- standard error) by day 4. Tyrosine hydroxylase (TH) mRNA levels were increased nearly 7-fold (686 +/- 71%) 24 hr after the first reserpine dose and declined thereafter. Northern blot analysis demonstrated that reserpine did not alter the size of either PPenk or TH mRNAs. Size exclusion chromatography showed a small (20%) reserpine-induced increase in processing of high molecular weight Penk-like peptides. The effects of reserpine, which increases PPenk mRNA, EC peptides, and TH mRNA, were completely blocked by unilateral denervation, whereas the contralateral innervated gland showed the expected responses. The co-localized EC peptide and catecholamine systems, as reflected in their mRNAs, respond differently in both time sequence and magnitude to reserpine and to denervation. Our results support a critical role, in vivo, for transsynaptic mechanisms in the maintenance of the high levels of Penk gene expression in this species and for the positive activation (mediated by reflex neurogenic stimulation) of reserpine on Penk and TH gene expression.
跨突触神经源性活动和利血平是两种可使前脑啡肽原(Penk)基因改变前脑啡肽原(PPenk)mRNA水平和含脑啡肽(EC)肽水平的信号。在叙利亚仓鼠肾上腺中,而非大鼠肾上腺中,这两种信号似乎都是Penk基因表达的正向激活剂。在仓鼠肾上腺中研究了利血平和去神经支配对EC肽和儿茶酚胺系统的单独及联合作用,仓鼠这种动物的肾上腺髓质PPenk mRNA和EC肽水平相对较高。单侧肾上腺去神经支配2天后,PPenk mRNA水平迅速下降54%,到11天时90%的Penk mRNA消失。4天后,EC肽和PPenk mRNA水平平行下降,而总RNA和可溶性蛋白水平未变。去神经支配直到术后8天才对TH mRNA水平产生影响,11天后TH mRNA和儿茶酚胺水平均下降了35 - 45%。利血平使EC肽和儿茶酚胺呈剂量和时间依赖性减少。在连续2天每天皮下注射5 mg/kg利血平1天后,EC肽减少80%,去甲肾上腺素减少79%,肾上腺素减少超过95%。治疗4天后,EC肽和儿茶酚胺水平略超过或已恢复到对照(同时给予赋形剂治疗)值。通过溶液杂交测量,到第4天PPenk mRNA水平增加了一倍(206 +/- 17%,平均值 +/- 标准误)。首次给予利血平剂量24小时后酪氨酸羟化酶(TH)mRNA水平增加近7倍(686 +/- 71%),此后下降。Northern印迹分析表明利血平未改变PPenk或TH mRNA的大小。尺寸排阻色谱显示利血平诱导高分子量脑啡肽样肽加工有小幅(20%)增加。增加PPenk mRNA、EC肽和TH mRNA的利血平作用被单侧去神经支配完全阻断,而对侧有神经支配的腺体显示出预期反应。共定位的EC肽和儿茶酚胺系统,从其mRNA反映来看,在时间顺序和幅度上对利血平和去神经支配的反应不同。我们的结果支持跨突触机制在该物种体内维持高水平Penk基因表达以及利血平对Penk和TH基因表达的正向激活(由反射性神经源性刺激介导)中起关键作用。