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
Objective: To study the effect of excited dopamine type I receptor on the production of nitric oxide/nitric oxide synthase(NO/NOS)in ox-LDL activated THP-1 cells and the possible mechanism.
Methods: Cultured THP-1 cells activated by PMA were randomly assigned in the following groups:control group (control), oxidized low density lipoprotein group (ox-LDL), dopamine receptor 1(DR1) agonist group (SKF), DR1 antagonist group (SCH), ERK blocker group (PD98059). Oil Red O staining was used to identify the accumulation of cellular lipid. The levels of NO and NOS in the supernatant of THP-1 were assayed by nitrate reductase method. The protein expression of DR1, p-ERK and ERK were obtained by Western blot and immunity fluorescence.
Results: After 48 h of incubation of ox-LDL, accumulation of lipid in the cytoplasm was found in most THP-1 cells. Compared with control group, DR1 protein expression was reduced in ox-LDL-induced cells(<0.01). Activation of DR1 agonist decrease the production of NO and iNOS(<0.01), and PD98059 partly reversed the above effect.
Conclusions: Activation of DR1 can inhibit the production of NO/NOS in ox-LDL-induced THP-1 cells, which may be related with ERK pathway.
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Source |
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http://dx.doi.org/10.13459/j.cnki.cjap.2016.03.022 | DOI Listing |
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