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促性腺激素释放激素的脉冲式刺激是增加促性腺激素亚基基因转录所必需的:体内脉冲频率对转录的差异调节证据。

A pulsatile gonadotropin-releasing hormone stimulus is required to increase transcription of the gonadotropin subunit genes: evidence for differential regulation of transcription by pulse frequency in vivo.

作者信息

Haisenleder D J, Dalkin A C, Ortolano G A, Marshall J C, Shupnik M A

机构信息

Department of Internal Medicine, University of Michigan, Ann Arbor 48109.

出版信息

Endocrinology. 1991 Jan;128(1):509-17. doi: 10.1210/endo-128-1-509.

Abstract

Previous results have shown that the pattern of GnRH pulses (amplitude and frequency) can differentially regulate expression of gonadotropin subunit cytoplasmic messenger RNA (mRNA) concentrations. The present study examined the effect of GnRH pulses on alpha, LH-beta and FSH-beta transcription rates as determined by nuclear runoff transcription assay. GnRH pulses (saline to controls) were given to castrate, testosterone-replaced male rats, and the rate of subunit gene transcription was measured in isolated pituitary nuclei. The effect of GnRH treatment duration was examined by giving GnRH pulses (25 ng/pulse at 30-min intervals) for 1, 4, or 24 h. The basal transcription rates [expressed as parts per million (ppm)] were 82 +/- 25 for alpha; 39 +/- 19 for LH-beta and 27 +/- 6 ppm for FSH-beta, and transcription rates of all 3 subunits were elevated at 1 h (3-5-fold vs. saline controls). After 4 h of GnRH pulses, alpha and FSH-beta transcription rates were reduced vs. 1 h, but LH-beta mRNA synthesis rate was maintained. At 24 h, the alpha transcription rate was still increased (66%), but LH-beta and FSH-beta transcription rates had fallen to basal levels despite the continuing pulsatile GnRH stimulus. The second experiment investigated the effect of the duration of GnRH pulses (25 ng/pulse, every 30 min for 4 h or 24 h), on cytoplasmic subunit mRNA concentrations to assess if the initial 4-h increase in transcription rate would induce a rise in cytoplasmic mRNAs. After 4 h of GnRH pulses, alpha and LH-beta mRNAs were unchanged, but FSH-beta mRNA had increased by 36% (P less than 0.05) compared to controls. All 3 subunit mRNAs were increased (approximately 2-fold) by 24 h of GnRH pulses. Administering GnRH pulses for 4 h followed by 20 h of saline pulses did not increase alpha mRNA; LH-beta was slightly increased (P less than 0.05), but FSH-beta mRNA concentrations were similar to levels seen after 24 h of continued GnRH pulses. The third experiment examined the effects of a continuous GnRH infusion and different GnRH pulse frequencies on gonadotropin subunit transcription rates. GnRH (25 ng/pulse) was given at intervals of 8, 30, or 120 min for 4 h (saline to controls). The continuous GnRH infusion (200 ng/h) did not increase the transcription rate of any of the three subunit mRNAs. alpha-subunit transcription rate was increased 2.7- or 4-fold by GnRH pulses given every 8 or 30 min, respectively.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

先前的研究结果表明,促性腺激素释放激素(GnRH)脉冲模式(幅度和频率)可不同程度地调节促性腺激素亚基细胞质信使核糖核酸(mRNA)浓度的表达。本研究通过核转录分析检测了GnRH脉冲对α、促黄体生成素β(LH-β)和促卵泡生成素β(FSH-β)转录率的影响。对去势并用睾酮替代的雄性大鼠给予GnRH脉冲(生理盐水作为对照),并在分离的垂体细胞核中测量亚基基因转录率。通过给予GnRH脉冲(每30分钟25纳克/脉冲)1、4或24小时,检测GnRH治疗持续时间的影响。基础转录率[以百万分之一(ppm)表示]:α为82±25;LH-β为39±19,FSH-β为27±6 ppm,所有3个亚基的转录率在1小时时均升高(比生理盐水对照高3至5倍)。GnRH脉冲4小时后,α和FSH-β转录率相对于1小时降低,但LH-β mRNA合成率维持不变。在24小时时,α转录率仍升高(66%),但尽管持续有GnRH脉冲刺激,LH-β和FSH-β转录率已降至基础水平。第二个实验研究了GnRH脉冲持续时间(每30分钟25纳克/脉冲,共4小时或24小时)对细胞质亚基mRNA浓度的影响,以评估转录率最初4小时的增加是否会导致细胞质mRNA升高。GnRH脉冲4小时后,α和LH-β mRNA未改变,但FSH-β mRNA与对照相比增加了36%(P<0.05)。GnRH脉冲24小时后,所有3个亚基mRNA均增加(约2倍)。给予GnRH脉冲4小时后再给予20小时生理盐水脉冲,α mRNA未增加;LH-β略有增加(P<0.05),但FSH-β mRNA浓度与持续GnRH脉冲24小时后的水平相似。第三个实验检测了持续GnRH输注和不同GnRH脉冲频率对促性腺激素亚基转录率的影响。以8、30或120分钟的间隔给予GnRH(25纳克/脉冲),持续4小时(生理盐水作为对照)。持续GnRH输注(200纳克/小时)未增加任何三种亚基mRNA的转录率。分别以每8分钟或30分钟给予GnRH脉冲,α亚基转录率增加2.7倍或4倍。(摘要截短至400字)

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