Neuroprotection by endogenous and exogenous PACAP following stroke

被引:97
作者
Chen, Yun
Samal, Babru
Hamelink, Carol R.
Xiang, Charlie C.
Chen, Yong
Chen, Mei
Vaudry, David
Brownstein, Michael J.
Hallenbeck, John M.
Eiden, Lee E.
机构
[1] NIH, Mol Neurosci Sect, Lab Cellular & Mol Regulat, Bethesda, MD 20892 USA
[2] NIMH, Genet Lab, NIH, Bethesda, MD 20892 USA
[3] NINDS, Stroke Branch, NIH, Bethesda, MD 20892 USA
关键词
pituitary adenylate cyclase activating polypeptide; PACAP; PACAP-deficient mouse; middle cerebral artery occlusion; MCAO; neurological severity score; NSS; cerebral ischerma; infarct volume; cDNA microarray; PACAP responsive gene; neuroprotection; neurotrauma;
D O I
10.1016/j.regpep.2006.06.016
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We investigated the effects of PACAP treatment, and endogenous PACAP deficiency, on infarct volume, neurological function, and the cerebrocortical transcriptional response in a mouse model of stroke, middle cerebral artery occlusion (MCAO). PACAP-38 administered i.v. or i.e. v. 1 h after MCAO significantly reduced infarct volume, and ameliorated functional motor deficits measured 24 h later in wild-type mice. Infarct volumes and neurological deficits (walking faults) were both greater in PACAP-deficient than in wild-type mice, but treatment with PACAP reduced lesion volume and neurological deficits in PACAP-deficient mice to the same level of improvement as in wild-type mice. A 35,546-clone mouse cDNA microarray was used to investigate cortical transcriptional changes associated with cerebral ischemia in wild-type and PACAP-deficient mice, and with PACAP treatment after MCAO in wild-type mice. 229 known (named) transcripts were increased (228) or decreased (1) in abundance at least 50% following cerebral ischemia, in wild-type mice. 49 transcripts were significantly up-regulated only at 1 h post-MCAO (acute response transcripts), 142 were up-regulated only at 24 h post-MCAO (delayed response transcripts) and 37 transcripts were upregulated at both times (sustained response transcripts). More than half of these are transcripts not previously reported to be altered in ischemia. A larger percentage of genes up-regulated at 24 hr than at 1 hr required endogenous PACAP, suggesting a more prominent role for PACAP in later response to injury than in the initial response. This is consistent with a neuroprotective role for PACAP in late response to injury, i.e., even when administered 1 hr or more after MCAO. Putative injury effector transcripts regulated by PACAP include beta-actin, rnidline 2, and metallothionein 1. Potential neuroprotective transcripts include several demonstrated to be PACAP-regulated in other contexts. Prominent among these were transcripts encoding the PACAP-regulated gene ler3, and the neuropeptides enkephalin, substance P (tachykinin 1), and neurotensin. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:4 / 19
页数:16
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