Indole-3-carbinol ameliorated the isoproterenol-induced myocardial infarction via multimodal mechanisms in Wistar rats

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dc.contributor.author Ramakrishna, Kakarla
dc.contributor.author Krishnamurthy, Sairam
dc.date.accessioned 2023-04-26T05:35:18Z
dc.date.available 2023-04-26T05:35:18Z
dc.date.issued 2022
dc.identifier.issn 14786419
dc.identifier.uri http://localhost:8080/xmlui/handle/123456789/2287
dc.description This paper is submitted by the author of IIT (BHU), Varanasi en_US
dc.description.abstract The present study investigated the cardioprotection of Indole-3-carbinol on isoproterenol (ISO)-induced myocardial infarction in Wistar rats. I3C treatment significantly reduced the prolongation of the QRS complex, QT interval, and ST-segment elevation. I3C was also able to normalise blood pressure (SBP, DBP, and MAP) and HR. I3C significantly decreased heart weight, cardiac troponin I (cTn I), CK-MB, LDH, AST and ALT. I3C ameliorated acute hyperglycaemia, hyperlipidemia, and myocardial infarction (%) in ISO rats. I3C treatment significantly elevated the antioxidant enzymes like SOD, CAT, and GSH and attenuated the MDA levels. I3C reduced the inflammatory cytokines (TNF-α and IL-6) and increased the anti-inflammatory cytokine 1 L-10. Furthermore, I3C significantly recovered myocardial structure by inhibiting neutrophil infiltration and oedema. Moreover, I3C attenuated apoptotic markers (cytochrome C, caspase 9 and caspase 3). Consequently, I3C restored cardiac function in MI rats by alleviating oxidative stress, inflammation, and apoptosis, and I3C could be used to treat myocardial infarction. en_US
dc.description.sponsorship Kakarla Ramakrishna is thankful to MHRD, India, for student fellowship and teaching assistantship through the Indian Institute of Technology (Banaras Hindu University), Varanasi. The authors also acknowledge Dr. A.N. Sahu for providing the semi-automated biochemical analyzer. en_US
dc.publisher Taylor and Francis Ltd. en_US
dc.relation.ispartofseries Natural Product Research;Volume 36, Issue 23, Pages 6044 - 6049
dc.subject apoptosis en_US
dc.subject Cruciferous vegetable en_US
dc.subject indole-3-carbinol en_US
dc.subject inflammation en_US
dc.subject isoproterenol en_US
dc.subject myocardial infarction en_US
dc.subject Animals en_US
dc.subject Indoles en_US
dc.subject Isoproterenol en_US
dc.subject Myocardial Infarction en_US
dc.subject Rats en_US
dc.subject Wistar en_US
dc.subject 3 indolemethanol en_US
dc.subject aspartate aminotransferase en_US
dc.subject caspase 3 en_US
dc.subject caspase 9 en_US
dc.subject catalase en_US
dc.subject creatine kinase MB en_US
dc.subject glutathione en_US
dc.subject interleukin 10 en_US
dc.subject interleukin 6 en_US
dc.subject lactate dehydrogenase en_US
dc.subject malonaldehyde en_US
dc.subject superoxide dismutase en_US
dc.subject tumor necrosis factor en_US
dc.subject isoprenaline en_US
dc.subject animal cell; apoptosis; Article; blood pressure measurement; cardiac muscle; controlled study; diastolic blood pressure; heart function; heart protection; heart rate; heart weight; hyperglycemia; hyperlipidemia; inflammation; isoproterenol-induced myocardial infarction; neutrophil chemotaxis; nonhuman; oxidative stress; QRS complex; QT prolongation; rat; ST segment elevation; systolic blood pressure; animal; heart infarction; Wistar rat en_US
dc.title Indole-3-carbinol ameliorated the isoproterenol-induced myocardial infarction via multimodal mechanisms in Wistar rats en_US
dc.type Article en_US


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