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: 1075
Function: getPubMedXML
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3195
Function: GetPubMedArticleOutput_2016
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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Persistent arterial hypertension (AHT) plays a very important role in the development of cardiovascular diseases (CVD). The present study assessed the vasodilator activities of the methanol extract (ME) and its fractions obtained from leaves of a Mexican plant. The fat- and tannin-free ME fraction (FTFME) produced the most potent vasodilator effect [EC 8.253 (4.672 to 14.58 μg/mL)], that was 6.7-fold higher than that of the ME [EC = 55.49 (29.78 to 68.69) μg/mL], which was similar to that of ACh used as a positive control. This effect was dependent on the nitric oxide/cGMP pathway. Six triterpene acids (ursolic, oleanolic, euscaphic, maslinic, corosolic, and alphitolic) were identified as the main constituents of this fraction. In contrast to the commercially available extracts, these compounds must be the most suitable chemical and pharmacological markers for this methanol extract in research into obtaining a standardised antihypertensive extract.
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http://dx.doi.org/10.1080/14786419.2025.2486334 | DOI Listing |