Severity: Warning
Message: file_get_contents(https://...@gmail.com&api_key=61f08fa0b96a73de8c900d749fcb997acc09&a=1): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests
Filename: helpers/my_audit_helper.php
Line Number: 197
Backtrace:
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 197
Function: file_get_contents
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 271
Function: simplexml_load_file_from_url
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3165
Function: getPubMedXML
File: /var/www/html/application/controllers/Detail.php
Line: 597
Function: pubMedSearch_Global
File: /var/www/html/application/controllers/Detail.php
Line: 511
Function: pubMedGetRelatedKeyword
File: /var/www/html/index.php
Line: 317
Function: require_once
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Thymoquinone (THQ), a strong antioxidant and anti-inflammatory bioactive compound has been reported in numerous studies to prevent the hepatorenal toxicity caused by various xenobiotics. Similarly, the zinc oxide nanoparticles (ZnONPs) have been used to protect against the hepatorenal damages caused by oxidative stress due to their potent antioxidant properties. The aim of this study was to synthesize and investigate the possible protective effects of THQ, ZnONPs and THQ-loaded ZnONPs against CCl induced hepatorenal toxicity in albino rats. ZnONPs and THQ-loaded ZnONPs were synthesized and characterized by various techniques. For the in-vivo study, thirty albino rats were randomly divided into five groups of six rats each. The control group received normal saline and 2 group (injury group) received CCl only. The 3 group (T1-group) received CCl + ZnONPs, the 4 group (T2-group) received CCl + THQ, and the 5 group (T3-group) received CCl + THQ-loaded ZnONPs. Renal and hepatic biomarkers (total bilirubin, AST, ALT, ALP, blood urea nitrogen and creatinine), lipid profiles, antioxidant levels and histopathological studies were investigated. The synthesized NPs showed a spherical shape with an average size of 16-30 nm and exhibited hexagonal structures. Results showed that THQ-loaded ZnONPs resulted in a decrease in liver and kidney biomarkers as well as a reduction in TC, TG, and LDL levels compared to groups received ZnONPs and THQ alone. CAT, SOD, GR and DPPH-radical scavenging ability were maintained at normal levels in group T3, which received THQ-loaded ZnONPs compared to T1 and T2 groups. Hepatic histopathological analysis revealed a reduction in hydropic degeneration and hepatocyte congestion in the central veins, alongside a decrease in tubular cell swelling and normalization of renal histology in the THQ-loaded ZnONPs groups. In conclusion, results of this investigation demonstrate that THQ-loaded ZnONPs can act as an efficient protectant and antioxidant against oxidative stress and hepatorenal toxicity caused by various xenobiotics.
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Source |
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11912352 | PMC |
http://dx.doi.org/10.1093/toxres/tfaf037 | DOI Listing |