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兴奋性氨基酸对青春期前雄性大鼠促性腺激素分泌的调控

Control of gonadotropin secretion in prepubertal male rats by excitatory amino acids.

作者信息

Aguilar E, Tena-Sempere M, Gonzalez D, Pinilla L

机构信息

Department of Physiology, Faculty of Medicine, University of Córdoba, Spain.

出版信息

Andrologia. 1996 May-Jun;28(3):163-9. doi: 10.1111/j.1439-0272.1996.tb02776.x.

Abstract

The role of N-methyl-D-aspartate (NMDA) and non-NMDA receptors in the control of FSH and LH secretion was analysed in prepubertal male rats. In the first experiment 4, 8, 12, 16, 20 and 30-day-old males were decapitated 15 min after vehicle, NMDA or kainic acid (KA) administration. In the second experiment, 23-day-old males were sham-orchidectomized or orchidectomized. Orchidectomized males were or were not implanted with silastic capsules containing testosterone and were sacrificed on day 30 after injection with vehicle, NMDA (15 mg kg-1), LHRH (100 ng rat-1), NMDA plus LHRH, or MK801, a non-competitive NMDA antagonist, (1 mg kg-1). In the third experiment, 30-day-old intact males pretreated with Nw-nitro-L-arginine methyl ester (NAME) or NG-methyl-L-arginine (MA), blockers of nitric oxide (NO) synthase, were sacrificed after NMDA or KA administration. In the fourth experiment, the effects of NMDA, KA, LHRH and NAME were analysed in monolayer cultures of dispersed adenohypophyseal cells. We found that: (i) NMDA and KA stimulated LH and FSH secretion in intact males; (ii) the NMDA effect on LH secretion remained after orchidectomy; (iii) FSH and LH responses to LHRH were not affected by simultaneous NMDA administration; (iv) antagonization of NMDA receptors with MK801 reduced the LH secretion in intact and orchidectomized males and blunted the FSH response to orchidectomy; (v) the stimulatory effect of NMDA or KA on LH secretion was not affected by pretreatment with blockers of NO synthase; (vi) the in vitro LH secretion remained unchanged after administration of NMDA, KA or NAME. We conclude that NMDA and non-NMDA receptors play a physiological role in the control of the basal and post-orchidectomy secretion of gonadotropins, and that this effects is independent of changes in NO generation and does not include changes in pituitary responsiveness to LHRH.

摘要

在青春期前雄性大鼠中分析了N-甲基-D-天冬氨酸(NMDA)和非NMDA受体在促卵泡激素(FSH)和促黄体生成素(LH)分泌控制中的作用。在第一个实验中,给4、8、12、16、20和30日龄的雄性大鼠分别注射溶剂、NMDA或海藻酸(KA),15分钟后断头处死。在第二个实验中,对23日龄的雄性大鼠进行假去势或去势手术。对去势的雄性大鼠,有的植入含睾酮的硅胶囊,有的未植入,在注射溶剂、NMDA(15 mg/kg)、促黄体生成素释放激素(LHRH,100 ng/只)、NMDA加LHRH或非竞争性NMDA拮抗剂MK801(1 mg/kg)后第30天处死。在第三个实验中,给30日龄的完整雄性大鼠预先注射一氧化氮(NO)合酶阻滞剂NNω�-硝基-L-精氨酸甲酯(NAME)或NG-甲基-L-精氨酸(MA),注射NMDA或KA后处死。在第四个实验中,在分散的腺垂体细胞单层培养物中分析NMDA、KA、LHRH和NAME的作用。我们发现:(i)NMDA和KA刺激完整雄性大鼠的LH和FSH分泌;(ii)去势后NMDA对LH分泌的作用仍然存在;(iii)同时给予NMDA不影响FSH和LH对LHRH的反应;(iv)用MK801拮抗NMDA受体可降低完整和去势雄性大鼠的LH分泌,并减弱FSH对去势的反应;(v)用NO合酶阻滞剂预处理不影响NMDA或KA对LH分泌的刺激作用;(vi)给予NMDA、KA或NAME后,体外LH分泌无变化。我们得出结论,NMDA和非NMDA受体在促性腺激素的基础分泌和去势后分泌的控制中发挥生理作用,且这种作用独立于NO生成的变化,也不包括垂体对LHRH反应性的变化。

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