Literature DB >> 21493898

Metabotropic regulation of RhoA/Rho-associated kinase by L-type Ca2+ channels: new mechanism for depolarization-evoked mammalian arterial contraction.

Miguel Fernández-Tenorio1, Cristina Porras-González, Antonio Castellano, Alberto Del Valle-Rodríguez, José López-Barneo, Juan Ureña.   

Abstract

BACKGROUND: Sustained vascular smooth muscle contraction is mediated by extracellular Ca(2+) influx through L-type voltage-gated Ca(2+) channels (VGCC) and RhoA/Rho-associated kinase (ROCK)-dependent Ca(2+) sensitization of the contractile machinery. VGCC activation can also trigger an ion-independent metabotropic pathway that involves G-protein/phospholipase C activation, inositol 1,4,5-trisphosphate synthesis, and Ca(2+) release from the sarcoplasmic reticulum (calcium channel-induced Ca(2+) release). We have studied the functional role of calcium channel-induced Ca(2+) release and the inter-relations between Ca(2+) channel and RhoA/ROCK activation. METHODS AND
RESULTS: We have used normal and genetically modified animals to study single myocyte electrophysiology and fluorimetry as well as cytosolic Ca(2+) and diameter in intact arteries. These analyses were complemented with measurement of tension and RhoA activity in normal and reversibly permeabilized arterial rings. We have found that, unexpectedly, L-type Ca(2+) channel activation and subsequent metabotropic Ca(2+) release from sarcoplasmic reticulum participate in depolarization-evoked RhoA/ROCK activity and sustained arterial contraction. We show that these phenomena do not depend on the change in the membrane potential itself, or the mere release of Ca(2+) from the sarcoplasmic reticulum, but they require the simultaneous activation of VGCC and the downstream metabotropic pathway with concomitant Ca(2+) release. During protracted depolarizations, refilling of the stores by a residual extracellular Ca(2+) influx through VGCC helps maintaining RhoA activity and sustained arterial contraction.
CONCLUSIONS: These findings reveal that calcium channel-induced Ca(2+) release has a major role in tonic vascular smooth muscle contractility because it links membrane depolarization and Ca(2+) channel activation with metabotropic Ca(2+) release and sensitization (RhoA/ROCK stimulation).

Entities:  

Mesh:

Substances:

Year:  2011        PMID: 21493898     DOI: 10.1161/CIRCRESAHA.111.240127

Source DB:  PubMed          Journal:  Circ Res        ISSN: 0009-7330            Impact factor:   17.367


  25 in total

1.  Rho-kinase expression in Hirschsprung's disease.

Authors:  David Coyle; Anne Marie O'Donnell; Nicolae Corcionivoschi; John Gillick; Prem Puri
Journal:  Pediatr Surg Int       Date:  2015-08-15       Impact factor: 1.827

2.  Age-dependent contribution of Rho kinase in carbachol-induced contraction of human detrusor smooth muscle in vitro.

Authors:  Timo Kirschstein; Chris Protzel; Katrin Porath; Tina Sellmann; Rüdiger Köhling; Oliver W Hakenberg
Journal:  Acta Pharmacol Sin       Date:  2013-10-14       Impact factor: 6.150

Review 3.  Smooth Muscle Ion Channels and Regulation of Vascular Tone in Resistance Arteries and Arterioles.

Authors:  Nathan R Tykocki; Erika M Boerman; William F Jackson
Journal:  Compr Physiol       Date:  2017-03-16       Impact factor: 9.090

Review 4.  Potassium Channels in Regulation of Vascular Smooth Muscle Contraction and Growth.

Authors:  W F Jackson
Journal:  Adv Pharmacol       Date:  2016-08-17

5.  Ca2+/calmodulin/MLCK pathway initiates, and RhoA/ROCK maintains, the internal anal sphincter smooth muscle tone.

Authors:  Satish Rattan
Journal:  Am J Physiol Gastrointest Liver Physiol       Date:  2016-12-08       Impact factor: 4.052

6.  Attenuation of monocyte chemotaxis--a novel anti-inflammatory mechanism of action for the cardio-protective hormone B-type natriuretic peptide.

Authors:  Nadezhda Glezeva; Patrick Collier; Victor Voon; Mark Ledwidge; Kenneth McDonald; Chris Watson; John Baugh
Journal:  J Cardiovasc Transl Res       Date:  2013-04-27       Impact factor: 4.132

Review 7.  Potential benefits of rho-kinase inhibition in arterial hypertension.

Authors:  Olaf Grisk
Journal:  Curr Hypertens Rep       Date:  2013-10       Impact factor: 5.369

8.  Disruption of K(2P)6.1 produces vascular dysfunction and hypertension in mice.

Authors:  Eric E Lloyd; Randy F Crossland; Sharon C Phillips; Sean P Marrelli; Anilkumar K Reddy; George E Taffet; Craig J Hartley; Robert M Bryan
Journal:  Hypertension       Date:  2011-08-29       Impact factor: 10.190

9.  Reduced vascular smooth muscle BK channel current underlies heart failure-induced vasoconstriction in mice.

Authors:  Elaine Wan; Jared S Kushner; Sergey Zakharov; Xiao-Wei Nui; Neelesh Chudasama; Christopher Kelly; Marc Waase; Darshan Doshi; Guoxia Liu; Shinichi Iwata; Takayuki Shiomi; Alexander Katchman; Jeanine D'Armiento; Shunichi Homma; Steven O Marx
Journal:  FASEB J       Date:  2013-01-16       Impact factor: 5.191

10.  Enhanced depolarization-induced pulmonary vasoconstriction following chronic hypoxia requires EGFR-dependent activation of NAD(P)H oxidase 2.

Authors:  Charles E Norton; Brad R S Broughton; Nikki L Jernigan; Benjimen R Walker; Thomas C Resta
Journal:  Antioxid Redox Signal       Date:  2012-10-18       Impact factor: 8.401

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.