DISTRIBUTION AND LOCALISATION OF Gα PROTEINS IN THE ROSTRAL VENTROLATERAL MEDULLA OF NORMOTENSIVE AND HYPERTENSIVE RATS: FOCUS ON CATECHOLAMINERGIC NEURONS

被引:6
|
作者
Parker, L. M. [1 ]
Tallapragada, V. J. [1 ]
Kumar, N. N. [1 ]
Goodchild, A. K. [1 ]
机构
[1] Macquarie Univ, Australian Sch Adv Med, Sydney, NSW 2109, Australia
基金
澳大利亚国家健康与医学研究理事会;
关键词
rostral ventrolateral medulla; rostral C1; A1; A5; G-proteins; spontaneously hypertensive rat; NUCLEOTIDE-BINDING PROTEIN; RECEPTOR-LIKE IMMUNOREACTIVITY; SYMPATHETIC-NERVE ACTIVITY; ADENYLYL CYCLASE SYSTEM; BRAIN-STEM; DIFFERENTIAL EXPRESSION; MESSENGER-RNA; IMMUNOHISTOCHEMICAL LOCALIZATION; NORADRENERGIC NEURONS; ALTERED EXPRESSION;
D O I
10.1016/j.neuroscience.2012.05.037
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
About 860 G-protein-coupled receptors (GPCRs) mediate their actions via heterotrimeric G-proteins. Their activation releases G alpha from G beta lambda subunits. The type of G alpha subunit dictates the major signalling proteins involved: adenylyl cyclase, PLC and rhoGEF. The rostral ventrolateral medulla (RVLM), containing the rostral C1 (rC1) cell group, sets and maintains the tonic and reflex control of blood pressure and a plethora of inputs converge onto these neurons. We determined the relative abundance of 10 G alpha subunit mRNAs, representing the four major families, within the RVLM, using quantitative RT-PCR. In situ hybridisation (ISH) combined with immunohistochemistry (IHC) was used to quantify and compare this expression in rC1 with that in the A1 and A5 cell groups. The relative abundance of G alpha subunit mRNAs and a comparison of gene expression levels were quantitatively determined in normotensive and hypertensive rat strains. All 10 G alpha mRNAs were detected in the RVLM of Sprague-Dawley (SD) rats with relative abundance such that G alpha s > G alpha i2 > G alpha o > G alpha q > G alpha L > G alpha 11 > G alpha i3 > G alpha i1 > G alpha 12 > G alpha 13. The high abundance of G alpha mRNAs signalling via adenylyl cyclase indicates the importance of associated GPCRs. Within the rC1 and A1 groups similar differential G alpha mRNA expression profiles were seen with G alpha s being found in all rC1 cells, G alpha 11 absent and G alpha i3 rarely expressed. Thus functionally distinct subgroups exist within the rC1 and A1 cell groups as differing distributions of G alpha subunits must reflect the array of GPCRs that influence their activity. In contrast, all A5 cells expressed all G alpha mRNAs suggesting a functionally homogeneous group. When the 10 G alpha mRNAs of the RVLM in spontaneously hypertensive rats (SHR) were compared quantitatively to Wistar-Kyoto (WKY), only G alpha s and G alpha 12 were significantly elevated. However when the expression in normotensive SD and WKY was compared with SHR no significant differences were evident. These findings demonstrate a range of GPCR signalling capabilities in brainstem neurons important for homeostasis and suggest a prominent role for signalling via adenylyl cyclase. (C) 2012 IBRO. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:20 / 34
页数:15
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