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A Doxorubicin-induced Cardiomyopathy Model in Adult Zebrafish
Published on: June 7, 2018
Multiomics Analysis Reveals the Protective Effect of a Novel Bioactive Peptide (BP1) in Cardiomyopathy Using a
Shweta Thakur1,2, Savita Kumari3,2, Ashwani Punia1,2
1Biotechnology Division, CSIR-Institute of Himalayan Bioresource Technology (IHBT), Palampur, Himachal Pradesh 176061, India.
A bioactive peptide (BP1) from Picrorhiza kurroa demonstrates significant cardioprotection against cardiac damage in zebrafish models. BP1 treatment targets multiple pathways, offering a novel therapeutic strategy for cardiovascular diseases.
Area of Science:
- Cardiovascular Research
- Pharmacology
- Zebrafish Models
Background:
- Medicinal plants are sources of bioactive peptides (BPs) with therapeutic potential.
- Bioactive peptide BP1 was isolated from Picrorhiza kurroa.
- BP1's cardioprotective role and metabolic control require system-level understanding.
Purpose of the Study:
- Investigate the cardioprotective effect of BP1.
- Assess BP1's efficacy in zebrafish models of isoproterenol- and doxorubicin-induced cardiac damage.
- Elucidate the molecular and metabolic mechanisms underlying BP1's cardioprotection.
Main Methods:
- Utilized zebrafish larvae and adult models for isoproterenol (ISO) and doxorubicin (DOX) induced cardiotoxicity.
- Evaluated cardiac morphology and function post-BP1 treatment.
- Performed transcriptomic and metabolomic analyses, including WGCNA.
Main Results:
- BP1 significantly reduced ISO-induced cardiac dysfunction in zebrafish larvae.
- BP1 pretreatment mitigated DOX-induced myocardial pathological changes.
- Transcriptomic and metabolomic data revealed BP1 targets protein synthesis, metabolic pathways, and cardiac contraction, attenuating cardiotoxicity.
Conclusions:
- BP1 exhibits significant cardioprotective effects in zebrafish models.
- BP1 acts via targeting multiple pathogenic pathways involved in cardiotoxicity.
- BP1 represents a promising therapeutic agent for cardiovascular protection.
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