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血管紧张素II在体外对垂体生长激素释放的刺激与抑制作用

Stimulation and inhibition of pituitary growth hormone release by angiotensin II in vitro.

作者信息

Robberecht W, Denef C

机构信息

Laboratory of Cell Pharmacology, University of Leuven School of Medicine, Campus Gasthuisberg, Belgium.

出版信息

Endocrinology. 1988 Apr;122(4):1496-504. doi: 10.1210/endo-122-4-1496.

Abstract

Rat pituitary cell aggregates cultured in serum-free chemically defined medium, single cells, and hemipituitaries were used in a perifusion system to study the influence of angiotensin II (AII) on GH release. In aggregates the peptide displayed both stimulatory and inhibitory effects on GH release, depending on the hormonal conditions of the culture medium and the age of the animal. When cultured in the absence of glucocorticoid, a modest but statistically significant stimulation was seen in aggregates from immature as well as adult animals. In aggregates from 5-day-old animals, dexamethasone (DEX) strongly enhanced the GH-releasing activity of AII in a dose-dependent way; in aggregates from 14- and 25-day-old rats, the same pattern was found, although the stimulatory action was weaker than the effect in 5-day-old rats. In aggregates from adult animals, the glucocorticoid established an inhibitory effect of AII on GH release, an effect seen with both low and high concentrations of DEX. These age- and DEX-dependent effects were not found for AII stimulation of PRL release. In the presence of DEX, AII also inhibited GRF-induced GH release in aggregates from adult animals, while it was synergistic with GRF in aggregates from developing animals. The effects of AII on GH release disappeared when aggregates were redispersed into single cells. However, in these single cell preparations AII strongly stimulated PRL release. In hemipituitaries from 1-, 5-, and 14-day-old animals, AII also stimulated GH release, but no effect was seen in hemipituitaries from 25-day-old and adult animals. These data indicate that AII has dual effects on GH release depending on the developmental stage of the animal and the hormonal environment. Furthermore, since no effect of AII was seen after redispersion of aggregates into single cells, both stimulatory and inhibitory effects seem to be based on an intercellular signaling system.

摘要

将在无血清化学限定培养基中培养的大鼠垂体细胞聚集体、单细胞和半垂体用于灌流系统,以研究血管紧张素II(AII)对生长激素(GH)释放的影响。在细胞聚集体中,该肽对GH释放显示出刺激和抑制作用,这取决于培养基的激素条件和动物的年龄。在无糖皮质激素的情况下培养时,未成熟和成年动物的细胞聚集体中均出现适度但具有统计学意义的刺激作用。在5日龄动物的细胞聚集体中,地塞米松(DEX)以剂量依赖的方式强烈增强了AII的GH释放活性;在14日龄和25日龄大鼠的细胞聚集体中也发现了相同的模式,尽管刺激作用比5日龄大鼠中的作用弱。在成年动物的细胞聚集体中,糖皮质激素对AII的GH释放产生抑制作用,低浓度和高浓度的DEX均可见此效应。AII对催乳素(PRL)释放的刺激作用未发现这些年龄和DEX依赖性效应。在存在DEX的情况下,AII还抑制成年动物细胞聚集体中生长激素释放因子(GRF)诱导的GH释放,而在发育中动物的细胞聚集体中它与GRF具有协同作用。当细胞聚集体重新分散为单细胞时,AII对GH释放的作用消失。然而,在这些单细胞制剂中,AII强烈刺激PRL释放。在1日龄、5日龄和14日龄动物的半垂体中,AII也刺激GH释放,但在25日龄和成年动物的半垂体中未观察到作用。这些数据表明,AII对GH释放具有双重作用,这取决于动物的发育阶段和激素环境。此外,由于细胞聚集体重新分散为单细胞后未观察到AII的作用,因此刺激和抑制作用似乎都基于细胞间信号系统。

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