β-Arrestin–Biased Angiotensin II Receptor Agonists for COVID-19-Reference-Cited by-同舟云学术

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β-Arrestin–Biased Angiotensin II Receptor Agonists for COVID-19

Published:2020-07-28 Issue:4 Volume:142 Page:318-320
ISSN:0009-7322
Container-title:Circulation
language:en
Short-container-title:Circulation

Author:

Manglik Aashish¹²,Wingler Laura M.³⁴,Rockman Howard A.³⁵,Lefkowitz Robert J.³⁴⁶^ORCID

Affiliation:

1. Department of Anesthesia and Perioperative Care (A.M.), University of California, San Francisco.

2. Department of Pharmaceutical Chemistry (A.M.), University of California, San Francisco.

3. Department of Medicine (L.M.W., H.A.R., R.J.L.), Duke University Medical Center, Durham, NC.

4. Howard Hughes Medical Institute (L.M.W., R.J.L.), Duke University Medical Center, Durham, NC.

5. Department of Cell Biology (H.A.R.), Duke University Medical Center, Durham, NC.

6. Department of Biochemistry (R.J.L.), Duke University Medical Center, Durham, NC.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

Reference5 articles.

1. β-Arrestin-biased AT1R stimulation promotes cell survival during acute cardiac injury

2. The renin–angiotensin system in acute respiratory distress syndrome

3. Acute respiratory distress syndrome leads to reduced ratio of ACE/ACE2 activities and is prevented by angiotensin-(1-7) or an angiotensin II receptor antagonist

4. Ang-(1-7) is an endogenous β-arrestin-biased agonist of the AT1 receptor with protective action in cardiac hypertrophy

5. Relationship between baseline systolic blood pressure and long-term outcomes in acute heart failure patients treated with TRV027: an exploratory subgroup analysis of BLAST-AHF

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4. The effect of TRV027 on coagulation in COVID‐19: A pilot randomized, placebo‐controlled trial;British Journal of Clinical Pharmacology;2022-12-14

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