Protection against Angiotensin II-induced endothelial dysfunction and hypertension via small molecule inhibitors of signal transducer and activator of transcription 3
Andrew William Johnson
University of Iowa
Doctor of Philosophy (PhD), University of Iowa
Spring 2012
DOI: 10.17077/etd.ydzu98x2
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<p>Angiotensin II (Ang II) promotes vascular disease and hypertension in part by the formation of pro-inflammatory cytokines, oxidative stress and inflammation. Signal transducer and activator of transcription 3 (STAT3) is a transcription factor known to play key roles in cytokine signaling and growth in immune cells. We tested the hypothesis that STAT3 plays an essential role in Ang II-induced vascular dysfunction and hypertension. Responses of carotid arteries from C57BL6 mice were examined in vitro after 22-hour incubation with vehicle or Ang II (10 nM) in the presence or absence of a small molecule inhibitor of STAT3 activation, S3I-201. The endothelium-dependent agonist acetylcholine (Ach) produced relaxation in arteries treated with vehicle and the response was inhibited by ~50% by Ang II (P<0.01). S3I-201 (10 πM) co-incubation prevented the Ang II-induced dysfunction. Relaxation to nitroprusside, an endothelium-independent agonist, was not altered in any group. Ang II increased vascular superoxide more than 2-fold (P<0.05) measured by chemiluminescence. S3I-201 (10 πM) prevented the Ang II induced increase of superoxide. Similar findings were obtained with STATTIC, a second small molecule inhibitor of STAT3 activation. In contrast to these findings, lipopolysaccharide (0.5 πg/ml)-induced endothelial dysfunction was not altered by S3I-201. Blood pressure and responses of carotid arteries and small resistance arteries within the brain were examined in C57BL6 mice with either saline or Ang II (1000 ng/kg/min) infused for 14 days via osmotic minipump, which were also treated with dimethyl sulfoxide (vehicle) or S3I-201 (5 mg/kg, IP, every two days). Infusion with Ang II increased systolic blood pressure compared to saline-infused animals (155±2 and 112±2 mmHg, respectively; P<0.001). S3I-201 reduced pressure slightly in saline infused mice but protected against Ang II-induced increase in pressure at 14 days (102±2 and 114±3 mmHg, respectively). Following systemic treatment with Ang II, carotid artery relaxation responses to Ach were significantly impaired compared to vehicle infused mice (72±3% and 101±1%, respectively, P<0.05). S3I-201 treatment significantly prevented Ang II-induced impairment (94±4%, P<0.05). Ang II treated mice exhibited 55% impaired dilator responses to Ach in small resistance arteries within the brain studied in vitro and S3I-201 treatment prevented most of this impairment (P<0.05). Vasorelaxation to nitroprusside was not altered in any group. In summary, these findings provide the first evidence that STAT3 plays an essential role in Ang II-induced vascular dysfunction and hypertension. Targeting STAT3 with small molecule inhibitors or other approaches may have beneficial effects during hypertension and other disease states in which Ang II contributes to vascular dysfunction (e.g. diabetes and aging).</p>
Pharmacology Angiotensin II Endothelial dysfunction S3I-201 Signal Transducer and Activator of Transcription 3 STAT3
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Title: Subtitle
Protection against Angiotensin II-induced endothelial dysfunction and hypertension via small molecule inhibitors of signal transducer and activator of transcription 3
Creators
Andrew William Johnson - University of Iowa
Contributors
Frank M. Faraci (Advisor)
Donald D. Heistad (Committee Member)
Kathryn G. Lamping (Committee Member)
Gary L. Baumbach (Committee Member)
Yuriy Usachev (Committee Member)
Resource Type
Dissertation
Degree Awarded
Doctor of Philosophy (PhD), University of Iowa
Degree in
Pharmacology
Date degree season
Spring 2012
Publisher
University of Iowa
DOI
10.17077/etd.ydzu98x2
Number of pages
xv, 157 pages
Copyright
Copyright 2012 Andrew William Johnson
Language
English
Description bibliographic
Includes bibliographical references (pages 122-157).
Academic Unit
Neuroscience and Pharmacology
Record Identifier
9983776939802771
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Protection against Angiotensin II-induced endothelial dysfunction