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Targeting PKGIα Cys(42) attenuates cardiac dysfunction in heart failure with preserved ejection fraction.

Targeting PKGIα Cys(42) attenuates cardiac dysfunction in heart failure with preserved ejection fraction.

期刊: Science advances 日期: 2026-08-21 PMID: 42616901 DOI: 10.1126/sciadv.aec8088 浏览: 12
作者: Su J, Zhao Y, Coleman P, Yang X, Holt M, Raabe J, Cuello F, Shah A, Shattock MJ, Zhang M
J, S., Y, Z., P, C., X, Y., M, H., J, R., F, C., A, S., MJ, S., & M, Z. (2026). Targeting PKGIα Cys(42) attenuates cardiac dysfunction in heart failure with preserved ejection fraction.. Science advances. https://doi.org/10.1126/sciadv.aec8088
J S, Y Z, P C, X Y, M H, J R, et al. Targeting PKGIα Cys(42) attenuates cardiac dysfunction in heart failure with preserved ejection fraction.. Science advances. 2026; doi: 10.1126/sciadv.aec8088
J S, Y Z, P C, et al. Targeting PKGIα Cys(42) attenuates cardiac dysfunction in heart failure with preserved ejection fraction.[J]. Science advances. 2026. DOI: 10.1126/sciadv.aec8088.
@article{j2026,
  author = {Su J and Zhao Y and Coleman P and Yang X and Holt M and Raabe J and Cuello F and Shah A and Shattock MJ and Zhang M},
  title = {Targeting PKGIα Cys(42) attenuates cardiac dysfunction in heart failure with preserved ejection fraction.},
  journal = {Science advances},
  year = {2026},
  doi = {10.1126/sciadv.aec8088},
  note = {PMID: 42616901},
}
TY  - JOUR
AU  - Su J
AU  - Zhao Y
AU  - Coleman P
AU  - Yang X
AU  - Holt M
AU  - Raabe J
AU  - Cuello F
AU  - Shah A
AU  - Shattock MJ
AU  - Zhang M
TI  - Targeting PKGIα Cys(42) attenuates cardiac dysfunction in heart failure with preserved ejection fraction.
T2  - Science advances
PY  - 2026
DO  - 10.1126/sciadv.aec8088
AN  - PMID:42616901
ER  - 

摘要

Heart failure with preserved ejection fraction (HFpEF) is a highly prevalent condition associated with substantial morbidity and mortality, yet effective therapeutic options remain limited. As oxidation of Cys42 in cyclic guanosine monophosphate (cGMP)-dependent protein kinase Iα (PKGIα) can enhance vessel and diastolic relaxation, processes impaired in HFpEF, we sought to target this mechanism using natural compounds with predicted thiol reactivity. Among these, urolithin A emerged as a compound with a previously unidentified and counterintuitive mode of action, directly modifying Cys42 in PKGIα. In a multihit HFpEF model that closely mimics the human condition, urolithin A improved diastolic function and attenuated cardiac remodeling through cysteine 42-dependent activation of PKGIα. These findings were further validated in human engineered heart tissue, where urolithin A enhanced both relaxation and contraction kinetics. These findings collectively highlight Cys42 in PKGIα as a promising therapeutic target for HFpEF and identify urolithin A as a previously unidentified activator of this protective mechanism.

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