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 |