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: 1057
Function: getPubMedXML
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3175
Function: GetPubMedArticleOutput_2016
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
In 52 patients with labile hypertension and also in experimental hypertension in 52 rats dynamics of kallikrein-kinin system in the blood during obsidan and hemiton treatment has been studied to find relationship between the hypotensive action of these drugs and the blood kinins activity. It was found that there exist counter-directional shifts in the kallikrein-kinin system of the blood as a result of treatment depending on their initial level. Adequate therapy contributed to the maintenance of optimum kinin concentration for preservation of homeostasis. With hypertensive syndrome supervening in rats increase of kinin predecessor synthesis has been recorded. Chronic administration of obsidan (0.5 mg/kg) and hemiton (0.1 mg/kg for 20 days increased kininogenesis).
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