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产前尼古丁暴露会改变新生大鼠脑干-脊髓标本中呼吸频率的甘氨酸能和γ-氨基丁酸能控制。

Prenatal nicotine exposure alters glycinergic and GABAergic control of respiratory frequency in the neonatal rat brainstem-spinal cord preparation.

作者信息

Luo Zili, McMullen Nathaniel T, Costy-Bennett Seres, Fregosi Ralph F

机构信息

Department of Physiology, The University of Arizona, Tucson, AZ 85721, USA.

出版信息

Respir Physiol Neurobiol. 2007 Aug 1;157(2-3):226-34. doi: 10.1016/j.resp.2007.01.005. Epub 2007 Jan 12.

Abstract

Bath application of GABA-A receptor agonists in neonatal rat brainstem-spinal cord preparations (BSSC) reduces respiratory frequency, an effect that is enhanced by prenatal nicotine exposure. Here we test the hypothesis that these effects can be reproduced by microinjection of GABAergic and glycinergic agonists into the pre-Botzinger complex region (PBC). We recorded the activity of phrenic motor axons from the fourth cervical ventral root in 1-3 days old BSSC that were exposed to either nicotine (6 mg/(kg day)) or saline prenatally. Microinjection of glycine or muscimol into the PBC caused abrupt, reversible apnea in all experiments. Apnea duration with glycine averaged 50.3+/-5 s in saline-exposed (N=12), and 95.7+/-9.9 s in nicotine-exposed (N=12) neonates (P<0.001). Apnea duration with muscimol averaged 51+/-5.1 s in saline-exposed (N=10), and 86+/-10.6 s in nicotine-exposed (N=12) neonates (P<0.05). These data show that prenatal nicotine exposure alters development of central ventilatory control, and that neurons in the PBC region are involved.

摘要

在新生大鼠脑干-脊髓标本(BSSC)中通过浴灌应用γ-氨基丁酸A(GABA-A)受体激动剂可降低呼吸频率,产前尼古丁暴露会增强这一效应。在此,我们检验以下假设:向脑桥前包钦格复合体区域(PBC)微量注射GABA能和甘氨酸能激动剂可再现这些效应。我们记录了1至3日龄BSSC中第四颈髓腹根膈运动轴突的活动,这些标本在产前要么暴露于尼古丁(6毫克/(千克·天)),要么暴露于生理盐水。在所有实验中,向PBC微量注射甘氨酸或蝇蕈醇均会导致突然的、可逆的呼吸暂停。在产前暴露于生理盐水的新生大鼠(N = 12)中,注射甘氨酸后的呼吸暂停持续时间平均为50.3±5秒,而在产前暴露于尼古丁的新生大鼠(N = 12)中为95.7±9.9秒(P<0.001)。在产前暴露于生理盐水的新生大鼠(N = 10)中,注射蝇蕈醇后的呼吸暂停持续时间平均为51±5.1秒,而在产前暴露于尼古丁的新生大鼠(N = 12)中为86±10.6秒(P<0.05)。这些数据表明,产前尼古丁暴露会改变中枢通气控制的发育,且PBC区域的神经元参与其中。

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