Pich E M, Agnati L F, Zini I, Marrama P, Carani C
Institute of Human Physiology, University of Modena, Italy.
Peptides. 1993 Sep-Oct;14(5):909-12. doi: 10.1016/0196-9781(93)90065-o.
The sedative and anxiolytic effects of intracerebroventricular administration of neuropeptide Y (NPY) were studied in spontaneously hypertensive rats (SHR) and in normotensive Wistar-Kyoto (WKy) rats using the two-compartment exploratory test, and in the open-field test after habituation. In the two-compartment tests, NPY produced anxiolytic effects by increasing the exploratory activity in SHR at a dose (0.25 nmol) lower than the minimal effective dose in WKy rats (1.25 nmol). In SHR, anxiolytic effects were observed for the whole NPY dose range (0.25-5.0 nmol), whereas in normotensive WKy rats the highest dose (5.0 nmol) failed to increase exploratory activity. The open-field test showed reduced locomotor activity and rearings in WKy rats when injected with 5.0 nmol NPY. These effects were not observed in SHR. The absence of sedative effects and the higher sensitivity to the anxiolytic effects of NPY in SHR are suggestive of a genetically determined difference in central NPY systems involved in behavioral adaptation that may be relevant for the development of hypertension.
采用双室探索性试验,对自发性高血压大鼠(SHR)和正常血压的Wistar - Kyoto(WKy)大鼠进行了侧脑室内注射神经肽Y(NPY)的镇静和抗焦虑作用研究,并在适应环境后进行旷场试验。在双室试验中,NPY以低于WKy大鼠最小有效剂量(1.25 nmol)的剂量(0.25 nmol)增加SHR的探索活动,从而产生抗焦虑作用。在SHR中,在整个NPY剂量范围(0.25 - 5.0 nmol)均观察到抗焦虑作用,而在正常血压的WKy大鼠中,最高剂量(5.0 nmol)未能增加探索活动。旷场试验显示,注射5.0 nmol NPY后,WKy大鼠的运动活动和竖尾次数减少。在SHR中未观察到这些效应。SHR中缺乏镇静作用以及对NPY抗焦虑作用的更高敏感性表明,参与行为适应的中枢NPY系统存在基因决定的差异,这可能与高血压的发生发展有关。