Bauer-Dantoin A C, McDonald J K, Levine J E
Department of Neurobiology and Physiology, Northwestern University, Evanston, Illinois 60208.
Endocrinology. 1991 Jul;129(1):402-8. doi: 10.1210/endo-129-1-402.
Recent evidence suggests that hypothalamic neurosecretion of neuropeptide Y (NPY) may be required for the preovulatory LH surge in female rats. Results of immunoneutralization and portal blood collection studies have suggested that NPY may serve to enhance the response of gonadotropes to the stimulatory action of LHRH. To directly test this hypothesis, the effects of NPY on LHRH-stimulated LH secretion were assessed in proestrous rats that were anesthetized with pentobarbital (PB) to block endogenous LHRH neurosecretion. Female rats were fitted with atrial catheters on diestrus. On proestrus, hourly blood samples were collected from 0900-2100 h. At 1330 h, rats received PB (40 mg/kg BW) or saline. Every 30 min from 1400-1800 h, PB-treated rats received iv pulses of LHRH (15, 150, or 1500 ng/pulse) or saline along with concurrent pulses of NPY (1 or 10 micrograms/pulse). Plasma samples were analyzed by LH RIA. In PB-treated rats receiving vehicle pulses only, LH surges were completely blocked. Pulsatile LHRH treatments at 15, 150, and 1500 ng/pulse produced subphysiological, physiological, and supraphysiological LH surges, respectively. Simultaneous administration of NPY pulses with 15 ng/pulse LHRH produced significant dose-related potentiations of LHRH-stimulated LH surges (P less than 0.0001). Administration of NPY pulses with 150 ng LHRH/pulse also significantly enhanced LHRH-induced LH surges (P less than 0.05). NPY RIA of plasma confirmed NPY increments after treatments. These results demonstrate that NPY administration can potentiate pituitary responsiveness to LHRH stimulation, and are consistent with the hypothesis that one function of NPY is to operate as a neurohormonal modulator at the level of the gonadotrope during generation of the preovulatory LH surge.
最近有证据表明,雌性大鼠排卵前促黄体生成素(LH)峰可能需要下丘脑神经分泌神经肽Y(NPY)。免疫中和及门静脉血采集研究结果表明,NPY可能有助于增强促性腺激素细胞对促性腺激素释放激素(LHRH)刺激作用的反应。为了直接验证这一假设,在戊巴比妥(PB)麻醉以阻断内源性LHRH神经分泌的动情前期大鼠中,评估了NPY对LHRH刺激的LH分泌的影响。雌性大鼠在动情间期植入心房导管。在动情前期,于09:00至21:00每小时采集一次血样。在13:30时,大鼠接受PB(40 mg/kg体重)或生理盐水。从14:00至18:00,每30分钟,接受PB处理的大鼠静脉注射LHRH脉冲(15、150或1500 ng/脉冲)或生理盐水,并同时注射NPY脉冲(1或10 μg/脉冲)。通过LH放射免疫分析(RIA)检测血浆样本。在仅接受溶剂脉冲的PB处理大鼠中,LH峰被完全阻断。15、150和1500 ng/脉冲的脉冲式LHRH处理分别产生亚生理、生理和超生理的LH峰。与15 ng/脉冲LHRH同时给予NPY脉冲产生了与剂量相关的显著LHRH刺激的LH峰增强作用(P<0.0001)。与150 ng LHRH/脉冲同时给予NPY脉冲也显著增强了LHRH诱导的LH峰(P<0.05)。血浆NPY RIA证实处理后NPY增加。这些结果表明,给予NPY可增强垂体对LHRH刺激的反应性,并且与以下假设一致,即NPY的一个功能是在排卵前LH峰产生期间作为促性腺激素细胞水平的神经激素调节剂发挥作用。