کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
6273932 | 1614815 | 2014 | 9 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Temporal changes in MrgC expression after spinal nerve injury
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کلمات کلیدی
DRGMRGGADPHCCICGRPSNLPBSdorsal root ganglion - گانگلیون ریشه پشتیchronic constriction injury - آسیب زدگی مزمنNerve injury - آسیب عصبیEDTA - اتیلن دی آمین تترا استیک اسید Ethylenediaminetetraacetic acid - اتیلینیدامین تتراستیک اسیدBAM - بمNeuropathic pain - درد نوروپاتیکPhosphate-buffered saline - محلول نمک فسفات با خاصیت بافریcalcitonin gene-related peptide - پپتید مرتبط با ژن کلسی تونینspinal nerve ligation - پیوند عصب ستون فقراتglyceraldehyde 3-phosphate dehydrogenase - گلیسرولیدید 3-فسفات دهیدروژنازbovine adrenal medulla - گوساله آدرنال مدولا
موضوعات مرتبط
علوم زیستی و بیوفناوری
علم عصب شناسی
علوم اعصاب (عمومی)
پیش نمایش صفحه اول مقاله
![عکس صفحه اول مقاله: Temporal changes in MrgC expression after spinal nerve injury Temporal changes in MrgC expression after spinal nerve injury](/preview/png/6273932.png)
چکیده انگلیسی
Mas-related G-protein-coupled receptor subtype C (MrgC) may play an important role in pain sensation. However, the distribution of MrgC receptors in different subpopulations of rodent dorsal root ganglion (DRG) neurons has not been clearly demonstrated owing to a lack of MrgC-selective antibody. It is also unclear whether peripheral nerve injury induces different time-dependent changes in MrgC expression in injured and uninjured DRG neurons. Here we showed that MrgC immunoreactivity is distributed in both IB4-positive (non-peptidergic) and calcitonin gene-related peptide-positive (peptidergic) DRG neurons in mice and rats. Importantly, the MrgC mRNA level and MrgC immunoreactivity were both decreased in the injured L5 DRG compared to corresponding levels in the contralateral (uninjured) DRG in rats on days 14 and 30 after an L5 spinal nerve ligation. In contrast, mRNA and protein levels of MrgC were increased in the adjacent uninjured L4 DRG. Thus, nerve injury may induce temporal changes in MrgC expression that differ between injured and uninjured DRG neurons. In animal behavior tests, chronic constriction injury of the sciatic nerve induced mechanical pain hypersensitivity in wild-type mice and Mrg-clusterÎâ/â mice (Mrg KO). However, the duration of mechanical hypersensitivity was longer in the Mrg KO mice than in their wild-type littermates, indicating that activation of Mrgs may constitute an endogenous mechanism that inhibits the maintenance of neuropathic pain in mice. These findings extend our knowledge about the distribution of MrgC in rodent DRG neurons and the regulation of its expression by nerve injury.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Neuroscience - Volume 261, 7 March 2014, Pages 43-51
Journal: Neuroscience - Volume 261, 7 March 2014, Pages 43-51
نویسندگان
S.-Q. He, L. Han, Z. Li, Q. Xu, V. Tiwari, F. Yang, X. Guan, Y. Wang, S.N. Raja, X. Dong, Y. Guan,