Neuropeptide Y3-36-loaded PVAX Nanoparticles Enhance Angiogenesis in Myocardial Ischemia

Background Neuropeptide Y (NPY) is an abundant sympathetic co-transmitter widely found in the heart, as it affects cardiac function. Purpose This study aimed to explore the effect of PVAX nanoparticles carrying NPY3-36 (PVAX-NPY3-36) on acute myocardial ischemia. Materials and Methods A double emulsification assay was conducted to load NPY3-36 onto the PVAX. With 11 untreated mice taken as a sham group, 38 mice were induced with left anterior descending artery ischemia, and some received PVAX-NPY3-36 or normal saline (Vehicle group). Upon evaluating heart function and echocardiographic data, all mouse tissues ( n = 49) were collected 2 weeks later for Western blot and real-time quantitative reverse transcription polymerase chain reaction (RT-qPCR) analyses. Results The presence of PVAX-NPY3-36 induced reduced infarct size and mortality ( p = .01 and p = .05), accompanied by increased systolic and diastolic parameters and elevation of stroke volume and cardiac function. Furthermore, upon treatment with PVAX-NPY3-36, ischemic tissues exhibited increased expression levels of pro-angiogenic factors. Conclusion Collectively, administration with NPY3-36 using PVAX nanoparticles promotes angiogenesis and alleviates the damage caused by myocardial ischemia.

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Journal
Pharmacognosy Magazine
Published
2025-08-25
DOI
https://doi.org/10.1177/09731296251367547
Primary Topic
Angiogenesis and VEGF in Cancer
Type
article
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article

Neuropeptide Y3-36-loaded PVAX Nanoparticles Enhance Angiogenesis in Myocardial Ischemia

Qing Li, Lini Zhao, Jiao Liu
Pharmacognosy Magazine
Angiogenesis and VEGF in Cancer
article

Neuropeptide Y3-36-loaded PVAX Nanoparticles Enhance Angiogenesis in Myocardial Ischemia

Qing Li, Lini Zhao, Jiao Liu
article en

Abstract

Background Neuropeptide Y (NPY) is an abundant sympathetic co-transmitter widely found in the heart, as it affects cardiac function. Purpose This study aimed to explore the effect of PVAX nanoparticles carrying NPY3-36 (PVAX-NPY3-36) on acute myocardial ischemia. Materials and Methods A double emulsification assay was conducted to load NPY3-36 onto the PVAX. With 11 untreated mice taken as a sham group, 38 mice were induced with left anterior descending artery ischemia, and some received PVAX-NPY3-36 or normal saline (Vehicle group). Upon evaluating heart function and echocardiographic data, all mouse tissues ( n = 49) were collected 2 weeks later for Western blot and real-time quantitative reverse transcription polymerase chain reaction (RT-qPCR) analyses. Results The presence of PVAX-NPY3-36 induced reduced infarct size and mortality ( p = .01 and p = .05), accompanied by increased systolic and diastolic parameters and elevation of stroke volume and cardiac function. Furthermore, upon treatment with PVAX-NPY3-36, ischemic tissues exhibited increased expression levels of pro-angiogenic factors. Conclusion Collectively, administration with NPY3-36 using PVAX nanoparticles promotes angiogenesis and alleviates the damage caused by myocardial ischemia.

Pharmacognosy Magazine
Taihe Hospital (CN), Hainan Medical University (CN)
Openalex Percentile: Top 80%
Angiogenesis and VEGF in Cancer
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