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Implantation of an Isoproterenol Mini-Pump to Induce Heart Failure in Mice
Published on: October 3, 2019
Isoproterenol-induced cardiac ischemia and fibrosis: Plant-based approaches for intervention
Prince Allawadhi1, Amit Khurana2, Nilofer Sayed2
1Department of Pharmacology, School of Pharmaceutical Education and Research (SPER), Jamia Hamdard, New Delhi, India.
Insights
This review explores plant-based compounds for heart protection against isoproterenol (ISP)-induced myocardial ischemia. These natural agents offer promising cardioprotective effects by targeting key molecular pathways involved in cardiac damage.
Area of Science:
- Cardiology
- Pharmacology
- Natural Product Research
Background:
- Myocardial infarction is a critical cardiac complication.
- Isoproterenol (ISP)-induced myocardial ischemia is a standard preclinical model for evaluating cardioprotective agents.
- Phytochemicals are increasingly recognized for their therapeutic potential in cardiovascular diseases.
Purpose of the Study:
- To provide an overview of the utility of ISP-induced cardiotoxicity, myocardial ischemia, and cardiac fibrosis in preclinical research.
- To survey the molecular mechanisms of various plant-based interventions screened for cardioprotective effects against ISP-induced cardiotoxicity.
- To summarize the probable mechanistic profiles of these phytochemical interventions.
Main Methods:
- Review of existing literature on phytochemicals and their effects on ISP-induced cardiotoxicity.
- Analysis of studies screening plant products like coriander, curcumin, Momordica, quercetin, and Withania somnifera.
- Examination of molecular pathways modulated by these phytochemicals, including reactive oxygen species scavenging, anti-inflammatory effects, and signaling pathway modulation (Nrf2, NFкB, PAK1, p-smad2/3).
Main Results:
- Several phytochemicals demonstrate efficacy in ameliorating ISP-induced myocardial ischemia.
- Mechanisms of protection involve antioxidant, anti-inflammatory actions, and modulation of critical molecular pathways.
- Plant-based compounds show potential in preventing cardiac damage and aiding cardiac remodeling.
Conclusions:
- Phytochemicals represent a viable therapeutic strategy for managing myocardial ischemia and cardiotoxicity.
- Understanding the molecular mechanisms of plant-based interventions is crucial for developing novel cardioprotective therapies.
- The ISP-induced model is valuable for preclinical screening of natural products for cardiac protection.
Abstract:
Heart is the most active and incumbent organ of the body, which maintains blood flow, but due to various pathological reasons, several acute and chronic cardiac complications arise out of which myocardial infarction is one of the teething problems. Isoproterenol (ISP)-induced myocardial ischemia is a classical model to screen the cardioprotective effects of various pharmacological interventions. Phytochemicals present a novel option for treating various human maladies including those of the heart. A large number of plant products and their active ingredients have been screened for efficacy in ameliorating ISP-induced myocardial ischemia including coriander, curcumin, Momordica, quercetin, and Withania somnifera. These phytochemicals constituents may play key role in preventing disease and help in cardiac remodeling. Reactive oxygen species scavenging, antiinflammatory, and modulation of various molecular pathways such as Nrf2, NFкB, p-21 activated kinase 1 (PAK1), and p-smad2/3 signaling modulation have been implicated behind the claimed protection. In this review, we have provided a focused overview on the utility of ISP-induced cardiotoxicity, myocardial ischemia, and cardiac fibrosis for preclinical research. In addition, we have also surveyed molecular mechanism of various plant-based interventions screened for cardioprotective effect in ISP-induced cardiotoxicity, and their probable mechanistic profile is summarized.
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