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The Effect of Sevoflurane Inhalation on Gabaergic Neurons Activation: Observation on the GAD67‐GFP Knock‐In Mouse
Author(s) -
Han LiChun,
Zhang Hui,
Wang Wei,
Wei YanYan,
Sun XingXing,
Yanagawa Youchio,
Li YunQing,
Xu LiXian,
Wu ShengXi
Publication year - 2010
Publication title -
the anatomical record: advances in integrative anatomy and evolutionary biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.678
H-Index - 62
eISSN - 1932-8494
pISSN - 1932-8486
DOI - 10.1002/ar.21113
Subject(s) - gabaergic , glutamate decarboxylase , sevoflurane , nucleus , medicine , arcuate nucleus , chemistry , neuroscience , hippocampus , endocrinology , biology , anesthesia , inhibitory postsynaptic potential , biochemistry , enzyme
Abstract The mechanisms underlying volatile anesthesia agents are not well elucidated. Emerging researches have focused on the participation of γ‐aminobutyric acid (GABA) neurons but there still lacks morphological evidence. To elucidate the possible activation of GABAergic neurons by sevoflurane inhalation in morphology, Fos (as neuronal activity marker) and GABA neurons double labeling were observed on the brain of glutamic acid decarboxylase (GAD) 67‐GFP knock‐in mice after sevoflurane inhalation. Twenty GAD67‐GFP knock‐in mice were divided into three groups: S1 group: incomplete anesthesia state induced by sevoflurane; S2 group: complete anesthesia state induced by sevoflurane; control(C) group. Sevoflurane induced a significant increase of Fos expression in the dorsomedial hypothalamic nucleus (DM), periaqueductal grey (PAG), hippocampus (CA1, DG), paraventricular thalamic nucleus (PV), lateral septal nucleus (LS), and cingulate cortex (Cg1 and Cg2) in S1 group compared to C group, and increase of Fos expression in S2 group compared to S1 group. In S2 group, Fos was only expressed in the medial amygdaloid nucleus (MeA), Edinger–Westphal (E–W) nucleus, arcuate hypothalamic nucleus (Arc) and the ventral part of paraventricular hypothalamic nucleus (PaV). Double immunofluroscent staining indicated that in LS, almost all Fos werepresent in GABAergic neurons. In CA1, DG, DM, cg1, cg2, and PAG, Fos was expressed as well, but only few were present in GABAergic neurons. Fos expression was very high in thalamus, but no coexistence were found as noGABAergic neuron was detected in this area. Our results provided morphological evidence that GABAergic transmission in specific brain areas may participate in the sevoflurane‐induced anesthesia. Anat Rec, 2010. © 2010 Wiley‐Liss, Inc.