cerebral ischemia;
in situ hybridization;
immunoblot;
electrophysiology;
G protein-linked neurotransmitter;
glutamatergic transmission;
hippocampus;
D O I:
10.1016/j.nbd.2005.05.011
中图分类号:
Q189 [神经科学];
学科分类号:
071006 ;
摘要:
In this study, we investigated whether transient cerebral ischemia affects the function and molecular expression of specific muscarinic cholinergic receptors. Our results show that in contrast to the GABA-R and A1 adenosine receptor systems, the ability of muscarinic receptors to attenuate evoked excitatory responses at vulnerable CA1 synapses is significantly attenuated by 18 h following reperfusion. This attenuation in efficacy was restricted to the vulnerable CA1 subfield, as no significant change in muscarinic receptor-mediated attenuation of evoked responsiveness was observed within post-ischemic dentate granule cell synapses. Expression analysis revealed that the mRNA and immunoreactive protein levels for individual types of muscarinic receptors respond differently, and uniquely to transient cerebral ischemia insult. Of particular interest is the m4 subtype of receptor, whose mRNA and protein expression levels were significantly diminished within the hippocampus by 12 and 24 h following reperfusion, respectively. As the m4 muscarinic receptor localizes to presynaptic terminals within the hippocampus, a decrease in its expression could account for the impaired functional responsiveness of the muscarinic receptor system following ischemic insult. Taken together, these results demonstrate that transient forebrain ischemia leads to dynamic alterations in the gene expression, protein prevalence, and functionality of muscarinic receptors in the post-ischemic hippocampus at times preceding the degeneration of the vulnerable neurons. (c) 2005 Elsevier Inc. All rights reserved.
机构:
Hallym Univ, Dept Biomed Sci, Chunchon 24252, South Korea
Hallym Univ, Res Inst Biosci & Biotechnol, Chunchon 24252, South Korea
Konkuk Univ, Coll Vet Med, Dept Anat, Seoul 05030, South Korea
Konkuk Univ, Vet Sci Res Inst, Seoul 05030, South KoreaSeoul Natl Univ, Coll Vet Med, Dept Anat & Cell Biol, Seoul 08826, South Korea
Kim, Woosuk
Hahn, Kyu Ri
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Seoul Natl Univ, Coll Vet Med, Dept Anat & Cell Biol, Seoul 08826, South Korea
Seoul Natl Univ, Res Inst Vet Sci, Seoul 08826, South KoreaSeoul Natl Univ, Coll Vet Med, Dept Anat & Cell Biol, Seoul 08826, South Korea
Hahn, Kyu Ri
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机构:
Kang, Min Soo
Kwon, Hyun Jung
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机构:
Hallym Univ, Dept Biomed Sci, Chunchon 24252, South Korea
Hallym Univ, Res Inst Biosci & Biotechnol, Chunchon 24252, South KoreaSeoul Natl Univ, Coll Vet Med, Dept Anat & Cell Biol, Seoul 08826, South Korea
Kwon, Hyun Jung
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机构:
Choi, Jung Hoon
Yoon, Yeo Sung
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机构:
Seoul Natl Univ, Coll Vet Med, Dept Anat & Cell Biol, Seoul 08826, South Korea
Seoul Natl Univ, Res Inst Vet Sci, Seoul 08826, South KoreaSeoul Natl Univ, Coll Vet Med, Dept Anat & Cell Biol, Seoul 08826, South Korea
Yoon, Yeo Sung
Kim, Dae Won
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Gangneung Wonju Natl Univ, Coll Dent, Res Inst Oral Sci, Dept Biochem & Mol Biol, Kangnung 25457, South KoreaSeoul Natl Univ, Coll Vet Med, Dept Anat & Cell Biol, Seoul 08826, South Korea
Kim, Dae Won
Yoo, Dae Young
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机构:
Soonchunhyang Univ, Coll Med, Dept Anat, Cheonan 31151, South KoreaSeoul Natl Univ, Coll Vet Med, Dept Anat & Cell Biol, Seoul 08826, South Korea
Yoo, Dae Young
Won, Moo-Ho
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Kangwon Natl Univ, Sch Med, Dept Neurobiol, Chunchon 24341, South KoreaSeoul Natl Univ, Coll Vet Med, Dept Anat & Cell Biol, Seoul 08826, South Korea
Won, Moo-Ho
Hwang, In Koo
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Seoul Natl Univ, Coll Vet Med, Dept Anat & Cell Biol, Seoul 08826, South Korea
Seoul Natl Univ, Res Inst Vet Sci, Seoul 08826, South KoreaSeoul Natl Univ, Coll Vet Med, Dept Anat & Cell Biol, Seoul 08826, South Korea