aFGF Targeted Mediated by Novel Nanoparticles-Microbubble Complex Combined With Ultrasound-Targeted Microbubble Destruction attenuates Doxorubicin-Induced Heart Failure via Anti-Apoptosis and Promoting Cardiac Angiogenesis

The purpose of this study was to evaluate the protective effect of acidic fibroblast growth factor targeted mediated by novel nanoparticles–cationic lipid microbubbles complex (aFGF–NP + CPMBs) combined with ultrasound targeted microbubble destruction (UTMD)on doxorubicin–induced heart failure (HF)a...

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Main Authors: Nan-Qian Zhou, Zhi-Xin Fang, Ning Huang, Yue Zuo, Yue Qiu, Li-Juan Guo, Ping Song, Jian Xu, Guang-rui Wan, Xin-Qiao Tian, Ya-ling Yin, Peng Li
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-04-01
Series:Frontiers in Pharmacology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fphar.2021.607785/full
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language English
format Article
sources DOAJ
author Nan-Qian Zhou
Nan-Qian Zhou
Nan-Qian Zhou
Zhi-Xin Fang
Zhi-Xin Fang
Zhi-Xin Fang
Ning Huang
Ning Huang
Ning Huang
Yue Zuo
Yue Qiu
Yue Qiu
Yue Qiu
Li-Juan Guo
Ping Song
Ping Song
Ping Song
Jian Xu
Jian Xu
Jian Xu
Guang-rui Wan
Guang-rui Wan
Guang-rui Wan
Xin-Qiao Tian
Ya-ling Yin
Peng Li
Peng Li
Peng Li
spellingShingle Nan-Qian Zhou
Nan-Qian Zhou
Nan-Qian Zhou
Zhi-Xin Fang
Zhi-Xin Fang
Zhi-Xin Fang
Ning Huang
Ning Huang
Ning Huang
Yue Zuo
Yue Qiu
Yue Qiu
Yue Qiu
Li-Juan Guo
Ping Song
Ping Song
Ping Song
Jian Xu
Jian Xu
Jian Xu
Guang-rui Wan
Guang-rui Wan
Guang-rui Wan
Xin-Qiao Tian
Ya-ling Yin
Peng Li
Peng Li
Peng Li
aFGF Targeted Mediated by Novel Nanoparticles-Microbubble Complex Combined With Ultrasound-Targeted Microbubble Destruction attenuates Doxorubicin-Induced Heart Failure via Anti-Apoptosis and Promoting Cardiac Angiogenesis
Frontiers in Pharmacology
doxorubicin
heart failure
aFGF-NP
anti-apoptotic
angiogenesis
UTMD
author_facet Nan-Qian Zhou
Nan-Qian Zhou
Nan-Qian Zhou
Zhi-Xin Fang
Zhi-Xin Fang
Zhi-Xin Fang
Ning Huang
Ning Huang
Ning Huang
Yue Zuo
Yue Qiu
Yue Qiu
Yue Qiu
Li-Juan Guo
Ping Song
Ping Song
Ping Song
Jian Xu
Jian Xu
Jian Xu
Guang-rui Wan
Guang-rui Wan
Guang-rui Wan
Xin-Qiao Tian
Ya-ling Yin
Peng Li
Peng Li
Peng Li
author_sort Nan-Qian Zhou
title aFGF Targeted Mediated by Novel Nanoparticles-Microbubble Complex Combined With Ultrasound-Targeted Microbubble Destruction attenuates Doxorubicin-Induced Heart Failure via Anti-Apoptosis and Promoting Cardiac Angiogenesis
title_short aFGF Targeted Mediated by Novel Nanoparticles-Microbubble Complex Combined With Ultrasound-Targeted Microbubble Destruction attenuates Doxorubicin-Induced Heart Failure via Anti-Apoptosis and Promoting Cardiac Angiogenesis
title_full aFGF Targeted Mediated by Novel Nanoparticles-Microbubble Complex Combined With Ultrasound-Targeted Microbubble Destruction attenuates Doxorubicin-Induced Heart Failure via Anti-Apoptosis and Promoting Cardiac Angiogenesis
title_fullStr aFGF Targeted Mediated by Novel Nanoparticles-Microbubble Complex Combined With Ultrasound-Targeted Microbubble Destruction attenuates Doxorubicin-Induced Heart Failure via Anti-Apoptosis and Promoting Cardiac Angiogenesis
title_full_unstemmed aFGF Targeted Mediated by Novel Nanoparticles-Microbubble Complex Combined With Ultrasound-Targeted Microbubble Destruction attenuates Doxorubicin-Induced Heart Failure via Anti-Apoptosis and Promoting Cardiac Angiogenesis
title_sort afgf targeted mediated by novel nanoparticles-microbubble complex combined with ultrasound-targeted microbubble destruction attenuates doxorubicin-induced heart failure via anti-apoptosis and promoting cardiac angiogenesis
publisher Frontiers Media S.A.
series Frontiers in Pharmacology
issn 1663-9812
publishDate 2021-04-01
description The purpose of this study was to evaluate the protective effect of acidic fibroblast growth factor targeted mediated by novel nanoparticles–cationic lipid microbubbles complex (aFGF–NP + CPMBs) combined with ultrasound targeted microbubble destruction (UTMD)on doxorubicin–induced heart failure (HF)and its mechanism. Heart failure rats induced by intraperitoneal injection with doxorubicin (DOX) to achieve cummulative dose of 15mg/kg for continuous 6 weeks showed left ventricular dysfunction, seriously oxidative stress, cardiomyocyte apoptosis, and decrease of myocardial vascular density. In contrast, aFGF–NP + CPMBs combined with UTMD therapy (3ug/kg, caudal vein injection, twice a week, 6weeks)prominently ameliorated left ventricular dysfunction by increased ejection fraction (EF) and fractional shortening (FS), decreased brain natriuretic peptide (BNP); strengthened the ability of antioxidant stress confirmed by increasing the activity of SOD and reducing the production of MDA; exerted the effect of anti–cardiomyocyte apoptosis and promotion angiogenesis by inhibited Bax expression and increased Bcl–2 expression and platelet endothelial cell adhesion molecule (CD31) expression. Taken together, the research suggested that aFGF targeted mediated by novel nanoparticles–cationic lipid microbubbles complex combined with UTMD should be a promising targeted treatment for heart failure.
topic doxorubicin
heart failure
aFGF-NP
anti-apoptotic
angiogenesis
UTMD
url https://www.frontiersin.org/articles/10.3389/fphar.2021.607785/full
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spelling doaj-bdbf18cbdf9c456590c304edb1d5cc8f2021-04-27T06:16:48ZengFrontiers Media S.A.Frontiers in Pharmacology1663-98122021-04-011210.3389/fphar.2021.607785607785aFGF Targeted Mediated by Novel Nanoparticles-Microbubble Complex Combined With Ultrasound-Targeted Microbubble Destruction attenuates Doxorubicin-Induced Heart Failure via Anti-Apoptosis and Promoting Cardiac AngiogenesisNan-Qian Zhou0Nan-Qian Zhou1Nan-Qian Zhou2Zhi-Xin Fang3Zhi-Xin Fang4Zhi-Xin Fang5Ning Huang6Ning Huang7Ning Huang8Yue Zuo9Yue Qiu10Yue Qiu11Yue Qiu12Li-Juan Guo13Ping Song14Ping Song15Ping Song16Jian Xu17Jian Xu18Jian Xu19Guang-rui Wan20Guang-rui Wan21Guang-rui Wan22Xin-Qiao Tian23Ya-ling Yin24Peng Li25Peng Li26Peng Li27Department of Ultrasonography, Henan Provincial People’s Hospital, People’s Hospital of Zhengzhou University, Zhengzhou, ChinaHenan International Joint Laboratory of Cardiovascular Remodeling and Drug Intervention, Xinxiang, China.Xinxiang Key Laboratory of Vascular Remodeling Intervention and Molecular Targeted Therapy Drug Development, Xinxiang, ChinaHenan International Joint Laboratory of Cardiovascular Remodeling and Drug Intervention, Xinxiang, China.Xinxiang Key Laboratory of Vascular Remodeling Intervention and Molecular Targeted Therapy Drug Development, Xinxiang, ChinaCollege of Pharmacy, Xinxiang Medical University, Xinxiang, ChinaHenan International Joint Laboratory of Cardiovascular Remodeling and Drug Intervention, Xinxiang, China.Xinxiang Key Laboratory of Vascular Remodeling Intervention and Molecular Targeted Therapy Drug Development, Xinxiang, ChinaCollege of Pharmacy, Xinxiang Medical University, Xinxiang, ChinaSchool of Basic Medical Sciences, Xinxiang Medical University, Xinxiang, ChinaHenan International Joint Laboratory of Cardiovascular Remodeling and Drug Intervention, Xinxiang, China.Xinxiang Key Laboratory of Vascular Remodeling Intervention and Molecular Targeted Therapy Drug Development, Xinxiang, ChinaCollege of Pharmacy, Xinxiang Medical University, Xinxiang, ChinaDepartment of Oncology, First Affiliated Hospital of Xinxiang Medical University, Xinxiang, ChinaHenan International Joint Laboratory of Cardiovascular Remodeling and Drug Intervention, Xinxiang, China.Xinxiang Key Laboratory of Vascular Remodeling Intervention and Molecular Targeted Therapy Drug Development, Xinxiang, ChinaCollege of Pharmacy, Xinxiang Medical University, Xinxiang, ChinaHenan International Joint Laboratory of Cardiovascular Remodeling and Drug Intervention, Xinxiang, China.Xinxiang Key Laboratory of Vascular Remodeling Intervention and Molecular Targeted Therapy Drug Development, Xinxiang, ChinaCollege of Pharmacy, Xinxiang Medical University, Xinxiang, ChinaHenan International Joint Laboratory of Cardiovascular Remodeling and Drug Intervention, Xinxiang, China.Xinxiang Key Laboratory of Vascular Remodeling Intervention and Molecular Targeted Therapy Drug Development, Xinxiang, ChinaCollege of Pharmacy, Xinxiang Medical University, Xinxiang, ChinaDepartment of Ultrasonography, Henan Provincial People’s Hospital, People’s Hospital of Zhengzhou University, Zhengzhou, ChinaSchool of Basic Medical Sciences, Xinxiang Medical University, Xinxiang, ChinaHenan International Joint Laboratory of Cardiovascular Remodeling and Drug Intervention, Xinxiang, China.Xinxiang Key Laboratory of Vascular Remodeling Intervention and Molecular Targeted Therapy Drug Development, Xinxiang, ChinaCollege of Pharmacy, Xinxiang Medical University, Xinxiang, ChinaThe purpose of this study was to evaluate the protective effect of acidic fibroblast growth factor targeted mediated by novel nanoparticles–cationic lipid microbubbles complex (aFGF–NP + CPMBs) combined with ultrasound targeted microbubble destruction (UTMD)on doxorubicin–induced heart failure (HF)and its mechanism. Heart failure rats induced by intraperitoneal injection with doxorubicin (DOX) to achieve cummulative dose of 15mg/kg for continuous 6 weeks showed left ventricular dysfunction, seriously oxidative stress, cardiomyocyte apoptosis, and decrease of myocardial vascular density. In contrast, aFGF–NP + CPMBs combined with UTMD therapy (3ug/kg, caudal vein injection, twice a week, 6weeks)prominently ameliorated left ventricular dysfunction by increased ejection fraction (EF) and fractional shortening (FS), decreased brain natriuretic peptide (BNP); strengthened the ability of antioxidant stress confirmed by increasing the activity of SOD and reducing the production of MDA; exerted the effect of anti–cardiomyocyte apoptosis and promotion angiogenesis by inhibited Bax expression and increased Bcl–2 expression and platelet endothelial cell adhesion molecule (CD31) expression. Taken together, the research suggested that aFGF targeted mediated by novel nanoparticles–cationic lipid microbubbles complex combined with UTMD should be a promising targeted treatment for heart failure.https://www.frontiersin.org/articles/10.3389/fphar.2021.607785/fulldoxorubicinheart failureaFGF-NPanti-apoptoticangiogenesisUTMD