PMID- 28383056 OWN - NLM STAT- MEDLINE DCOM- 20181116 LR - 20211204 IS - 2045-2322 (Electronic) IS - 2045-2322 (Linking) VI - 7 DP - 2017 Apr 6 TI - Involvement of Epithelial Na(+) Channel in the Elevated Myogenic Response in Posterior Cerebral Arteries from Spontaneously Hypertensive Rats. PG - 45996 LID - 10.1038/srep45996 [doi] LID - 45996 AB - Hypertension is characterized by increased peripheral vascular resistance which is related with elevated myogenic response. Recent findings have indicated that epithelial sodium channel (ENaC) is involved in mechanotransduction of the myogenic response. The purpose of this study was to investigate the involvement of ENaC in the elevated myogenic response of posterior cerebral arteries (PCAs) from spontaneously hypertensive rats (SHRs). Sixteen to eighteen weeks old male wistar kyoto rats (WKYs) and SHRs were used in this study. We found that wall to lumen (W/L) ratio was increased in the PCAs from SHRs compared with WKYs at the resting state. Interestingly, amiloride significantly inhibited myogenic response in the PCAs from SHRs and WKYs, however, the magnitude of the blockade was greater in SHRs. The transfection of gammaENaC-siRNA significantly reduced the expression of gammaENaC protein and inhibited myogenic response in the PCAs from SHRs. Furthermore, these data were supported by the findings that serum/glucocorticoid-induced kinase (Sgk1) and neural precursor cell-expressed developmentally downregulated gene 4-2 (Nedd4-2) were increased in SHRs compared with WKYs. Our results suggest that gammaENaC may play an important role in the elevated myogenic response in PCAs from SHRs. FAU - Choi, Soo-Kyoung AU - Choi SK AD - Department of Physiology, College of Medicine, Brain Korea 21 Plus Project for Medical Sciences, Yonsei University, Seoul, Korea. FAU - Yeon, Soo-In AU - Yeon SI AD - Department of Physiology, College of Medicine, Brain Korea 21 Plus Project for Medical Sciences, Yonsei University, Seoul, Korea. FAU - Kwon, Youngin AU - Kwon Y AD - Department of Physiology, College of Medicine, Brain Korea 21 Plus Project for Medical Sciences, Yonsei University, Seoul, Korea. FAU - Byeon, Seonhee AU - Byeon S AD - Department of Physiology, College of Medicine, Brain Korea 21 Plus Project for Medical Sciences, Yonsei University, Seoul, Korea. FAU - Lee, Young-Ho AU - Lee YH AD - Department of Physiology, College of Medicine, Brain Korea 21 Plus Project for Medical Sciences, Yonsei University, Seoul, Korea. LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20170406 PL - England TA - Sci Rep JT - Scientific reports JID - 101563288 RN - 0 (Epithelial Sodium Channels) RN - 0 (Immediate-Early Proteins) RN - 0 (Protein Subunits) RN - 0 (RNA, Small Interfering) RN - 7DZO8EB0Z3 (Amiloride) RN - EC 2.3.2.26 (NEDD4L protein, rat) RN - EC 2.3.2.26 (Nedd4 Ubiquitin Protein Ligases) RN - EC 2.7.11.1 (Protein Serine-Threonine Kinases) RN - EC 2.7.11.1 (serum-glucocorticoid regulated kinase) SB - IM MH - Amiloride/pharmacology MH - Animals MH - Epithelial Sodium Channels/*metabolism MH - Immediate-Early Proteins/metabolism MH - Male MH - *Muscle Development MH - Nedd4 Ubiquitin Protein Ligases/metabolism MH - Phosphorylation MH - Posterior Cerebral Artery/*metabolism MH - Principal Component Analysis MH - Protein Serine-Threonine Kinases/metabolism MH - Protein Subunits/metabolism MH - RNA, Small Interfering/metabolism MH - Rats, Inbred SHR MH - Rats, Inbred WKY PMC - PMC5382693 COIS- The authors declare no competing financial interests. EDAT- 2017/04/07 06:00 MHDA- 2018/11/18 06:00 PMCR- 2017/04/06 CRDT- 2017/04/07 06:00 PHST- 2017/01/05 00:00 [received] PHST- 2017/03/07 00:00 [accepted] PHST- 2017/04/07 06:00 [entrez] PHST- 2017/04/07 06:00 [pubmed] PHST- 2018/11/18 06:00 [medline] PHST- 2017/04/06 00:00 [pmc-release] AID - srep45996 [pii] AID - 10.1038/srep45996 [doi] PST - epublish SO - Sci Rep. 2017 Apr 6;7:45996. doi: 10.1038/srep45996.