Danger J M, Breton B, Vallarino M, Fournier A, Pelletier G, Vaudry H
European Institute for Peptide Research, CNRS URA 650 UA INSERM, University of Rouen, Mont-Saint-Aignan, France.
Endocrinology. 1991 May;128(5):2360-8. doi: 10.1210/endo-128-5-2360.
Using a specific antiserum raised against synthetic neuropeptide-Y (NPY), the distribution of NPY-like immunoreactivity in the brain and pituitary of the trout Oncorhynchus mykiss has been examined with the indirect immunofluorescence and peroxidase-antiperoxidase methods. The highest density of NPY-immunoreactive elements was found in the basal telencephalon and hypothalamus. In particular, NPY-immunoreactive neurons were located in the nucleus entopeduncularis and the preoptic nucleus. NPY-immunoreactive fibers were observed throughout the trout brain. The preoptic nucleus, the suprachiasmatic nucleus, and the nucleus entopeduncularis were densely innervated. In addition, NPY-positive fibers were detected in the nucleus lateralis tuberis and in the distal and intermediate lobes of the pituitary. The NPY-like peptide of the trout brain was characterized by combining HPLC analysis and radioimmunological detection. Serial dilutions of trout hypothalamus and pituitary extracts produced displacement curves that were parallel to the standard curve. HPLC analysis resolved a major peak which was slightly less hydrophobic than porcine NPY. The possible effect of NPY, either alone or in combination with a GnRH antagonist, on gonadotropin (GtH) release from trout pituitaries was investigated using a perifusion system technique. Graded concentrations of synthetic NPY induced a dose-dependent stimulation of GtH release. The stimulatory activities of NPY and various short chain analogs on GtH release were compared: the order of potency was NPY greater than NPY-(2-36) greater than NPY-(16-36) greater than NPY-(25-36). This result suggests that the biological determinant of NPY is located in the C-terminal part of the molecule. Administration of a short pulse of NPY or GnRH (10(-7) M each) induced a marked stimulation of GtH release. Prolonged infusion of the GnRH antagonist D-Phe2-6,Pro3-GnRH induced a significant reduction of GnRH-evoked GtH secretion. In addition, the GnRH antagonist blocked NPY-induced GtH release. The widespread distribution of NPY in the trout brain suggests the involvement of this neuropeptide in a variety of physiological functions. The present data support the view that NPY, released by nerve terminals in the distal lobe of the pituitary, may act presynaptically on GnRH fibers to modulate GtH release.
利用针对合成神经肽Y(NPY)制备的特异性抗血清,采用间接免疫荧光法和过氧化物酶-抗过氧化物酶法,研究了虹鳟脑和垂体中NPY样免疫反应性的分布。在基底端脑和下丘脑发现了NPY免疫反应性元素的最高密度。特别是,NPY免疫反应性神经元位于内缰核和视前核。在整个虹鳟脑中均观察到NPY免疫反应性纤维。视前核、视交叉上核和内缰核接受密集的神经支配。此外,在垂体结节外侧核以及垂体远侧叶和中间叶检测到NPY阳性纤维。通过高效液相色谱(HPLC)分析和放射免疫检测对虹鳟脑的NPY样肽进行了表征。虹鳟下丘脑和垂体提取物的系列稀释产生了与标准曲线平行的置换曲线。HPLC分析分离出一个主峰,其疏水性略低于猪NPY。使用灌流系统技术研究了NPY单独或与促性腺激素释放激素(GnRH)拮抗剂联合对虹鳟垂体促性腺激素(GtH)释放的可能影响。合成NPY的分级浓度诱导了GtH释放的剂量依赖性刺激。比较了NPY和各种短链类似物对GtH释放的刺激活性:效力顺序为NPY大于NPY-(2-36)大于NPY-(16-36)大于NPY-(25-36)。该结果表明NPY的生物学决定因素位于分子的C末端部分。给予短脉冲的NPY或GnRH(各10^-7 M)可显著刺激GtH释放。长期输注GnRH拮抗剂D-Phe2-6,Pro3-GnRH可显著降低GnRH诱发的GtH分泌。此外,GnRH拮抗剂阻断了NPY诱导的GtH释放。NPY在虹鳟脑中的广泛分布表明该神经肽参与多种生理功能。目前的数据支持这样的观点,即垂体远侧叶神经末梢释放的NPY可能在突触前作用于GnRH纤维以调节GtH释放。