Rasmussen D D
Department of Reproductive Medicine, University of California at San Diego, La Jolla 92093-0802.
Neuroendocrinology. 1993 Nov;58(5):511-8. doi: 10.1159/000126584.
Several studies have demonstrated that the rat isolated mediobasohypothalamus can release gonadotropin-releasing hormone (GnRH) in a pulsatile manner in vitro. We have now used an in vitro perfusion system to characterize GnRH release from the adult male Sprague-Dawley rat isolated median eminence (ME) alone. After 1 h stabilization periods, eight MEs released GnRH in an episodic pattern during 4-hour experiments (samples collected every 4 min, RIA in triplicate) with mean (+/- SE) release rates of 2.2 +/- 0.2 pg GnRH/4 min and peak amplitudes of 1.3 +/- 0.2 pg/4 min. The intervals between significant peaks were variable, although 70% were in the range of 12-24 min, i.e. similar to the non-gonadal steroid-modulated frequency of pulsatile luteinizing hormone secretion in gonadectomized rats in vivo. During nine additional experiments, MEs were perifused with control medium (containing 2.5 mM calcium) through the first hour of sample collection, then either calcium-free medium containing 0.5 mM of the calcium chelator EGTA and 100 microM of the intracellular calcium antagonist TMB-8 or calcium-free medium containing just 100 microM TMB-8 for 2 h, followed by a final hour with control medium. Removal of calcium activity decreased the frequency of GnRH peaks from 3.2 +/- 0.3 to 1.3 +/- 0.2/h, which then increased to 2.3 +/- 0.3/h with subsequent replacement of control medium. Removal of available calcium also decreased mean GnRH release by 51 +/- 11%, which returned to basal levels with subsequent calcium replacement.(ABSTRACT TRUNCATED AT 250 WORDS)
多项研究表明,大鼠离体的中基底下丘脑在体外能以脉冲方式释放促性腺激素释放激素(GnRH)。我们现在使用体外灌注系统来单独研究成年雄性Sprague-Dawley大鼠离体正中隆起(ME)释放GnRH的特性。在1小时的稳定期后,8个ME在4小时的实验中以间歇性模式释放GnRH(每4分钟采集样本,一式三份进行放射免疫测定),平均(±标准误)释放速率为2.2±0.2 pg GnRH/4分钟,峰值幅度为1.3±0.2 pg/4分钟。显著峰值之间的间隔是可变的,尽管70%在12 - 24分钟范围内,即类似于去性腺大鼠体内非性腺类固醇调节的促黄体生成素脉冲分泌频率。在另外9个实验中,在样本采集的第一个小时,ME用对照培养基(含2.5 mM钙)进行灌注,然后用含0.5 mM钙螯合剂EGTA和100 μM细胞内钙拮抗剂TMB - 8的无钙培养基或仅含100 μM TMB - 8的无钙培养基灌注2小时,随后最后一个小时用对照培养基灌注。去除钙活性使GnRH峰值频率从3.2±0.3降至1.3±0.2/小时,随后更换对照培养基后又增至2.3±0.3/小时。去除可利用的钙也使GnRH平均释放量降低了51±11%,随后钙替代后又恢复到基础水平。(摘要截短于250字)