Severity: Warning
Message: file_get_contents(https://...@pubfacts.com&api_key=b8daa3ad693db53b1410957c26c9a51b4908&a=1): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests
Filename: helpers/my_audit_helper.php
Line Number: 176
Backtrace:
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 176
Function: file_get_contents
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 250
Function: simplexml_load_file_from_url
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3122
Function: getPubMedXML
File: /var/www/html/application/controllers/Detail.php
Line: 575
Function: pubMedSearch_Global
File: /var/www/html/application/controllers/Detail.php
Line: 489
Function: pubMedGetRelatedKeyword
File: /var/www/html/index.php
Line: 316
Function: require_once
The p-glycoprotein is a transmembrane efflux transporter found on the luminal side of the capillary endothelial cells that comprise the blood-brain barrier. This study examined the effect of CJY, an isoflavone, on the levels of a p-glycoprotein substrate, rhodamine123 (Rh123), in rat brain microvessel endothelial cells (RBMEC) and in rat brain homogenate using fluorescence spectrophotometer and high performance liquid chromatography, respectively. In the in vitro study, incubation of RBMEC cells with CJY caused a marked increase in uptake and a notable decrease in efflux of Rh123. The inhibitory effect of the agent on P-gp function was reversible and remained even after the 2.5microM agent was removed from the medium for 120 min. In the in vivo study, CJY also elevated the Rh123 levels in rat brain homogenate after the rats received a 0.45 mg/kg dose of the CJY by slow intravenous injection, indicating that CJY may be a candidate as a p-glycoprotein inhibitor.
Download full-text PDF |
Source |
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http://dx.doi.org/10.1179/joc.2008.20.3.361 | DOI Listing |
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