Table · dataset · 2026
Table 1_Effects of candesartan on cellular redox status and bioenergetics of cardiac tissue in normal and chronically stressed rats.docx
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Background<p>Studies of redox status and bioenergetics in cardiac tissue during unpredictable chronic mild stress (UCMS) are scarce.
Description
The present study examined the effect of candesartan, an angiotensin II type 1 receptor (AT1R) blocker primarily used to treat hypertension and congestive heart failure, on the antioxidant capacity and energy homeostasis of cardiac tissue in UCMS-subjected rats.</p>Methods<p>Forty-eight male Wistar rats were randomly assigned to four groups (n = 12/group): undosed normal controls (NC), UCMS-subjected rats (UCMS), unstressed candesartan-treated rats (Can), and stressed candesartan-treated rats (UCMS + Can).
Enzyme activities and mRNA transcripts of key antioxidant enzymes, tricarboxylic acid cycle enzymes, and respiratory chain complexes were measured in myocardial tissue, together with oxidative-phosphorylation (OXPHOS) markers, redox state, and the energy-homeostasis ratios GSH/GSSG, NAD<sup>+</sup>/NADH, and ATP/ADP.</p>Results<p>The UCMS group showed marked elevations in oxidative-stress markers, accompanied by significantly reduced antioxidant enzyme activities and downregulated antioxidant gene expression.
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In parallel, all TCA-cycle and OXPHOS enzyme activities were significantly decreased, and their relative gene transcripts were markedly downregulated. The cellular GSH/GSSG and ATP/ADP ratios were significantly lowered, whereas the NAD<sup>+</sup>/NADH ratio was increased. Each of these changes was either fully reversed or significantly attenuated in unstressed and stressed rats receiving candesartan.</p>Conclusion<p>Candesartan clearly mitigates cellular oxidative stress and the disruption of energy metabolism in the myocardial tissue of UCMS-subjected rats.
Because blood pressure, cardiac function and systemic haemodynamics were not measured, these findings should be interpreted as biochemical evidence of a cytoprotective action of AT1R blockade in myocardial tissue, and they provide a preliminary rationale for further evaluation of candesartan in stress-related cardiovascular disorders.</p>
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Where it is published
- DOI doi.org/10.3389/fphar.2026.1876050.s001 ↗
DOI / persistent id · from figshare com
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- OAI-PMH record api.figshare.com/v2/oai?verb=GetRecord&metadataPrefix=oai_dc&identifier=oai%3Af… ↗
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Topics
Provenance · 1 source records, 18 field assertions
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