Differential Impact of Dilator Stimuli on Increased Myogenic Activation of Cerebral and Skeletal Muscle Resistance Arterioles in Obese Zucker Rats. (12th October 2013)
- Record Type:
- Journal Article
- Title:
- Differential Impact of Dilator Stimuli on Increased Myogenic Activation of Cerebral and Skeletal Muscle Resistance Arterioles in Obese Zucker Rats. (12th October 2013)
- Main Title:
- Differential Impact of Dilator Stimuli on Increased Myogenic Activation of Cerebral and Skeletal Muscle Resistance Arterioles in Obese Zucker Rats
- Authors:
- Butcher, Joshua T.
Goodwill, Adam G.
Stanley, Shyla C.
Frisbee, Jefferson C. - Abstract:
- <abstract abstract-type="main" id="micc12056-abs-0001"> <title>Abstract</title> <sec id="micc12056-sec-0001" sec-type="section"> <title>Objective</title> <p>To use the OZR model of the metabolic syndrome to determine the impact of dilator stimuli on MA of GA and MCA. We tested the hypothesis that increased oxidant stress and TxA<sub>2</sub> exacerbate MA, and prevent its blunting with dilator stimuli, in OZR.</p> </sec> <sec id="micc12056-sec-0002" sec-type="section"> <title>Methods</title> <p>GA/MCA from OZR and LZR was pressurized <italic>ex vivo</italic>. MA was determined under control conditions and following challenge with acetylcholine, hypoxia, and adenosine. Responses were also evaluated after pre‐treatment with TEMPOL (antioxidant) and SQ‐29548 (PGH<sub>2</sub>/TxA<sub>2</sub> receptor antagonist).</p> </sec> <sec id="micc12056-sec-0003" sec-type="section"> <title>Results</title> <p>MA was increased (and dilator responses decreased) in GA/MCA from OZR, dependent on the endothelium and ROS. In GA, the impact of ROS on MA and dilator effects was largely via TxA<sub>2</sub>, while in MCA, this appeared was more dependent on NO bioavailability. Intrinsic responses of GA/MCA to carbacyclin, U46619, and NO donors were similar between strains.</p> </sec> <sec id="micc12056-sec-0004" sec-type="section"> <title>Conclusions</title> <p>A developing ROS‐based endothelial dysfunction in MCA and GA of OZR contributes to an enhanced MA of these vessels. Although treatment of<abstract abstract-type="main" id="micc12056-abs-0001"> <title>Abstract</title> <sec id="micc12056-sec-0001" sec-type="section"> <title>Objective</title> <p>To use the OZR model of the metabolic syndrome to determine the impact of dilator stimuli on MA of GA and MCA. We tested the hypothesis that increased oxidant stress and TxA<sub>2</sub> exacerbate MA, and prevent its blunting with dilator stimuli, in OZR.</p> </sec> <sec id="micc12056-sec-0002" sec-type="section"> <title>Methods</title> <p>GA/MCA from OZR and LZR was pressurized <italic>ex vivo</italic>. MA was determined under control conditions and following challenge with acetylcholine, hypoxia, and adenosine. Responses were also evaluated after pre‐treatment with TEMPOL (antioxidant) and SQ‐29548 (PGH<sub>2</sub>/TxA<sub>2</sub> receptor antagonist).</p> </sec> <sec id="micc12056-sec-0003" sec-type="section"> <title>Results</title> <p>MA was increased (and dilator responses decreased) in GA/MCA from OZR, dependent on the endothelium and ROS. In GA, the impact of ROS on MA and dilator effects was largely via TxA<sub>2</sub>, while in MCA, this appeared was more dependent on NO bioavailability. Intrinsic responses of GA/MCA to carbacyclin, U46619, and NO donors were similar between strains.</p> </sec> <sec id="micc12056-sec-0004" sec-type="section"> <title>Conclusions</title> <p>A developing ROS‐based endothelial dysfunction in MCA and GA of OZR contributes to an enhanced MA of these vessels. Although treatment of GA/MCA with TEMPOL attenuates MA in OZR, the mechanistic contributors to altered MA, distal to ROS, differ between the two resistance vessels.</p> </sec> </abstract> … (more)
- Is Part Of:
- Microcirculation. Volume 20:Number 7(2013:Oct.)
- Journal:
- Microcirculation
- Issue:
- Volume 20:Number 7(2013:Oct.)
- Issue Display:
- Volume 20, Issue 7 (2013)
- Year:
- 2013
- Volume:
- 20
- Issue:
- 7
- Issue Sort Value:
- 2013-0020-0007-0000
- Page Start:
- 579
- Page End:
- 589
- Publication Date:
- 2013-10-12
- Subjects:
- Biological transport -- Periodicals
Microcirculation -- Physiology -- Periodicals
612.135 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1549-8719/issues ↗
http://onlinelibrary.wiley.com/ ↗
http://informahealthcare.com/loi/mic ↗ - DOI:
- 10.1111/micc.12056 ↗
- Languages:
- English
- ISSNs:
- 1073-9688
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5758.460000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 4334.xml