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: 1034
Function: getPubMedXML
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3152
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
Osteoporosis is one of the main health problems in the world today characterized by low bone mass and deterioration in bone microarchitecture. In recent years, the use of natural products approach to treat it has been in the increase. In this study, antiosteoporosis activity and hepatotoxicity of . bark extracts were evaluated. . Mouse bone marrow macrophage (BMM) cells were incubated with tartrate-resistant acid phosphate (TRAP) buffers and -nitrophenyl phosphate and cultured with different . bark extracts at concentrations of 0, 6.25, 12.5, 25, and 50 g/ml in the presence of the receptor activator of nuclear factor kappa-Β ligand (RANKL) for 6 days. The osteoclast TRAP activity and cell viability were measured. Nitric oxide (NO) assay was conducted using murine macrophage-like RAW 264.7 cells treated with . ethanolic and methanolic bark extracts at concentrations of 0, 6.25, 12.5, 25, 50, 100, and 200 g/ml. For hepatotoxicity assessment, zebrafish larvae were exposed to . bark extracts, 0.05% dimethyl sulfoxide as a negative control, and 5 M tamoxifen as a positive control. The surviving larvae were anesthetized and assessed for hepatocyte apoptosis. . TRAP activity was significantly inhibited ( < 0.001) at all concentrations of . extracts compared to the control treatment. At 50 g/ml, both ethanolic and methanolic extracts of . exhibited significant ( < 0.01) BMM cell viability compared to the control treatment. . ethanolic and methanolic extracts had significant inhibitory ( < 0.01) effects on lipopolysaccharide (LPS)-induced NO production at 200 g/ml and exhibited significant ( < 0.01) and ( < 0.05) stimulative effects, respectively, on RAW 264.7 cell viability. No overt hepatotoxicity was observed in the liver of zebrafish larvae in any of the treatments. . The TRAP activity of . bark gives a foundation for further studies to enhance future development of antiosteoporosis drug.
Download full-text PDF |
Source |
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7532380 | PMC |
http://dx.doi.org/10.1155/2020/8582318 | DOI Listing |
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