Cerebral Arteriogenesis is Enhanced by Pharmacological as Well as Fluid-Shear-Stress Activation of the Trpv4 Calcium Channel

Schierling, W. and Troidi, K. and Apfelbeck, H. and Troidl, C. and Kasprzak, P. M. and Schaper, W. and Schmitz-Rixen, T. (2011) Cerebral Arteriogenesis is Enhanced by Pharmacological as Well as Fluid-Shear-Stress Activation of the Trpv4 Calcium Channel. EUROPEAN JOURNAL OF VASCULAR AND ENDOVASCULAR SURGERY, 41 (5). pp. 589-596. ISSN 1078-5884,

Full text not available from this repository. (Request a copy)

Abstract

Objectives: This study aimed to determine the importance of the shear-stress-sensitive calcium channels Trpc1, Trpm7, Trpp2, Trpv2 (transient receptor potential cation channel, subfamily V, member 2) and Trpv4 for cerebral arteriogenesis. The expression profiles were analysed, comparing the stimulation of collateral growth by target-specific drugs to that achieved by maximum increased fluid shear stress (FSS). Design: A prospective, controlled study wherein rats were subjected to bilateral carotid artery ligature (BCL), or BCL + arteriovenous fistula, or BCL + drug application. Methods: Messenger RNA (mRNA) abundance and protein expression were determined in FSS-stimulated cerebral collaterals by quantitative real-time polymerase chain reaction (qRT-PCR) and immunohistochemistry. Drugs were applied via osmotic mini pumps and arteriogenesis was evaluated by post-mortem angiograms and Ki67 immunostaining. Results: Trpv4 was the only mechanosensitive Trp channel showing significantly increased mRNA abundance and protein expression after FSS stimulation. Activation of Trpv4 by 4 alpha-phorbol-12,13-didecanoate caused significantly enhanced collateral growth (length: 4.43 +/- + 0.20 mm and diameter: 282.6 +/- 8.1 mu m) compared with control (length: 3.80 +/- 0.06 mm and diameter: 237.3 +/- 5.3 mu m). Drug application stimulated arteriogenesis to almost the same extent as did maximum FSS stimulation (length: 4.61 +/- 0.07 mm and diameter: 327.4 +/- 12.6 mu m). Conclusions: Trpv4 showed significantly increased expression in FSS-stimulated cerebral collaterals. Pharmacological Trpv4 activation enhanced cerebral arteriogenesis, pinpointing Trpv4 as a possible candidate for the development of new therapeutic concepts. (C) 2010 European Society for Vascular Surgery. Published by Elsevier Ltd. All rights reserved.

Item Type: Article
Uncontrolled Keywords: COLONY-STIMULATING FACTOR; CAROTID-ARTERY OCCLUSION; RECEPTOR POTENTIAL CHANNELS; HYPOPERFUSED RAT-BRAIN; VESSEL GROWTH; CIRCULATION; DISEASE; FLOW; Arteriogenesis; Brain; Collateral circulation; Fluid shear stress; Trpv4; Rat
Subjects: 600 Technology > 610 Medical sciences Medicine
Divisions: Medicine > Abteilung für Gefäßchirurgie
Depositing User: Dr. Gernot Deinzer
Date Deposited: 22 Jun 2020 05:57
Last Modified: 22 Jun 2020 05:57
URI: https://pred.uni-regensburg.de/id/eprint/20849

Actions (login required)

View Item View Item