Day J C, Koehl M, Deroche V, Le Moal M, Maccari S
Psychobiologie des Comportements Adaptatifs, Institut National de la Santé et de la Recherche Médicale Unité 259, Université Victor Segalen Bordeaux 2, 33077 Bordeaux Cedex, France.
J Neurosci. 1998 Mar 1;18(5):1886-92. doi: 10.1523/JNEUROSCI.18-05-01886.1998.
There is growing evidence that stressors occurring during pregnancy can impair biological and behavioral responses to stress in the adult offspring. For instance, prenatal stress enhances emotional reactivity, anxiety, and depressive-like behaviors associated with a prolonged stress-induced corticosterone secretion and a reduction in hippocampal corticosteroid receptors. Among the neurotransmitters involved in these hormonal and behavioral responses, acetylcholine may play a critical role. However, it is unknown whether prenatal stressful events also may influence the development of cholinergic systems. In the present study, hippocampal acetylcholine was measured, by in vivo microdialysis, in both male and female adult prenatally stressed rats, under basal conditions, after a mild stress (saline injection) or after intracerebroventricular administration of corticotropin-releasing factor (CRF; 0.1 nM). No difference in basal release of acetylcholine was observed between control and prenatally stressed rats of both genders. Mild stress was found to increase hippocampal acetylcholine release to a greater extent in prenatally stressed rats than in controls. In males, the CRF-induced increase in hippocampal acetylcholine release was larger in prenatally stressed rats, as compared with controls, during the first hour after the injection and in females during the third hour after the injection. These data indicate that prenatal stress has long-term effects on the development of forebrain cholinergic systems. The augmented increase in hippocampal acetylcholine release after the mild stress and CRF injection in prenatally stressed rats may be involved in some of the hormonal and behavioral abnormalities found in prenatally stressed rats.
越来越多的证据表明,孕期发生的应激源会损害成年后代对应激的生物学和行为反应。例如,产前应激会增强情绪反应性、焦虑和类似抑郁的行为,这与应激诱导的皮质酮分泌延长以及海马体糖皮质激素受体减少有关。在参与这些激素和行为反应的神经递质中,乙酰胆碱可能起关键作用。然而,产前应激事件是否也会影响胆碱能系统的发育尚不清楚。在本研究中,通过体内微透析法,在基础条件下、轻度应激(注射生理盐水)后或脑室内注射促肾上腺皮质激素释放因子(CRF;0.1 nM)后,测量了成年雄性和雌性产前应激大鼠海马体中的乙酰胆碱含量。在对照大鼠和产前应激大鼠中,未观察到两性之间乙酰胆碱基础释放量的差异。发现轻度应激使产前应激大鼠海马体中的乙酰胆碱释放量比对照大鼠增加得更多。在雄性大鼠中,与对照大鼠相比,产前应激大鼠在注射后第一小时,CRF诱导的海马体乙酰胆碱释放增加幅度更大;在雌性大鼠中,在注射后第三小时增加幅度更大。这些数据表明,产前应激对前脑胆碱能系统的发育具有长期影响。产前应激大鼠在轻度应激和CRF注射后海马体乙酰胆碱释放量的增强增加,可能与产前应激大鼠中发现的一些激素和行为异常有关。