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
Objective: To evaluate the lymphocyte apoptotic impact of yellow laser light in vitro.
Methods: The experimental study was conducted from November 2021 to April 2022 at the Postgraduate Medical Physics Laboratory, Mustansiriyah University, Baghdad, Iraq, and comprised blood samples from healthy volunteers. The samples were subjected to 1:1 dilution in isotonic phosphate buffered saline, and each sample was divided into two equal aliquots; one for irradiation, and other as control.The percentage of apoptotic lymphocyte was estimated before and after radiation exposure with low-level laser 589nm at 30J/cm², 50J/cm² and 70J/cm² energy intensities. Post-exposure evaluation was done immediately, and 1 and 2 hours after radiation on the viability of normal human cells. The vitality of the cells was determined using the trypan blue exclusion test. Data was analysed using SPSS 24.
Results: There were 26 healthy volunteers (16 male, 10 females) with an age range of (20-40) years. After the exposure, the percentage of lymphocytes that apoptose increased significantly when cells were irradiated at 70J/cm2 immediately compared to the controls (p≤ 0.05), but there was no significant differences with the 30J/cm² dose. After 1 and 2 hours, a significant reduction in the proportion of apoptotic lymphocytes was observed (p<0.05).
Conclusions: Yellow low-level laser showed a noticeable protective effect on lymphocytes by decreasing the percentage of dead cells.
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Source |
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http://dx.doi.org/10.47391/JPMA-BAGH-16-45 | DOI Listing |
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