Adenosine A1R/A3R agonist AST-004 reduces brain infarction in mouse and rat models of acute ischemic stroke
- 1Department of Cell Systems and Anatomy, University of Texas Health at San Antonio, San Antonio, TX, United States
- 2NeuroVasc Preclinical Services, Inc., Lexington, MA, United States
- 3Astrocyte Pharmaceuticals Inc., Cambridge, MA, United States
A corrigendum on
Adenosine A1R/A3R agonist AST-004 reduces brain infarction in mouse and rat models of acute ischemic stroke
by Fisher, E. S., Chen, Y., Sifuentes, M. M., Stubblefield, J. J., Lozano, D., Holstein, D. M., Ren, J., Davenport, M., DeRosa, N., Chen, T. -p., Nickel, G., Liston, T. E., and Lechleiter, J. D. (2022). Front. Stroke 1:1010928. doi: 10.3389/fstro.2022.1010928
In the published article, there was an error in the Funding statement. The funding source for coauthor Jeremy J. Stubblefield was not included. Original text: This study received funding from Astrocyte Pharmaceuticals, Inc. The correct Funding statement appears below.
Funding
This study received funding from Astrocyte Pharmaceuticals, Inc. JS was supported by NIH IRACDA training grant K12 GM111726.
The authors apologize for this error and state that this does not change the scientific conclusions of the article in any way. The original article has been updated.
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Keywords: Adora3, stroke treatment, mitochondrial metabolism, ATP, astrocytes
Citation: Fisher ES, Chen Y, Sifuentes MM, Stubblefield JJ, Lozano D, Holstein DM, Ren J, Davenport M, DeRosa N, Chen T-p, Nickel G, Liston TE and Lechleiter JD (2024) Corrigendum: Adenosine A1R/A3R agonist AST-004 reduces brain infarction in mouse and rat models of acute ischemic stroke. Front. Stroke 3:1371734. doi: 10.3389/fstro.2024.1371734
Received: 16 January 2024; Accepted: 18 January 2024;
Published: 29 January 2024.
Approved by:
Frontiers Editorial Office, Frontiers Media SA, SwitzerlandCopyright © 2024 Fisher, Chen, Sifuentes, Stubblefield, Lozano, Holstein, Ren, Davenport, DeRosa, Chen, Nickel, Liston and Lechleiter. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: James D. Lechleiter, lechleiter@uthscsa.edu
†These authors share first authorship