Carthamus tinctorius l. Inhibits proliferation of lung cancer A549 cells and tender’s mitochondrial protection (Record no. 17338)

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040 ## - CATALOGING SOURCE
Original cataloging agency AIKTC-KRRC
Transcribing agency AIKTC-KRRC
100 ## - MAIN ENTRY--PERSONAL NAME
9 (RLIN) 17617
Author Dailah, Hamad Ghaleb
245 ## - TITLE STATEMENT
Title Carthamus tinctorius l. Inhibits proliferation of lung cancer A549 cells and tender’s mitochondrial protection
250 ## - EDITION STATEMENT
Volume, Issue number Vol.56(3), Jul-Sep
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Place of publication, distribution, etc. Karnataka
Name of publisher, distributor, etc. Association of Pharmaceutical Teachers of India (APTI)
Year 2022
300 ## - PHYSICAL DESCRIPTION
Pagination 789-794p.
520 ## - SUMMARY, ETC.
Summary, etc. Background: Plant-based products are well-known as long-lasting chemo preventive and
chemotherapeutic medicines against cancer. Objectives: The purpose of this research
is to identify out how safflower extract affects A549 cells. Materials and Methods:
The antiproliferative activity was determined using the Trypan blue assay, while the
cytotoxicity was determined using the MTT assay. The ethidium bromide/acridine
orange (AO/EB) dual staining method was used to observe the apoptotic inducing effect
and the morphological assessment of A549 cells using phase contrast microscopy
was studied to discern the nuclear changes if any on treatment with safflower.
The mitochondrial membrane potential was studied using a cationic lipophilic dye
rhodamine 123 under a confocal microscope, and oxidative stress was assessed using
2’,7’-dichlorodihydrofluorescein diacetate (DCFH-DA) labelling. Results: The trypan blue
assay speculated that there was a decrease in cell viability at highest concentration and
that the effect was dose dependent. The MTT assay revealed that cytotoxicity increases
in cells treated with higher concentration. The LC50 range of the sample was found at
250 μg/ml concentration at 52.2%, whereas the viability of the cell declined to 28.19%
at 350μg/ml concentration. The morphological features like shrinkage, detachment,
membrane blebbing, and distorted shape were observed on safflower treated A549 cells
that supports the antiproliferative activity. The ethidium bromide and acridine orange
staining substantiates that safflower extract induces apoptosis wherein the untreated
A549 cells showed green fluorescence with intact nuclear morphology and cells treated
with safflower extract (200 μg and 250 μg/ml), showed apoptotic bodies, clearly
validating the apoptosis inducing effect by safflower on A549 cells. Also, the safflower
extract protects the mitochondria by decreasing the oxidative stress and by altering the
mitochondrial membrane potential. Conclusion: Thus, it is found that safflower extract
exerts its antiproliferative activity by inducing apoptosis and protects mitochondria by
combating oxidative stress.
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
9 (RLIN) 4639
Topical term or geographic name entry element PHARMACEUTICS
773 0# - HOST ITEM ENTRY
Place, publisher, and date of publication Bengluru Association of Pharmaceutical Teachers of India (APTI)
International Standard Serial Number 0019-5464
Title Indian journal of pharmaceutical education and research
856 ## - ELECTRONIC LOCATION AND ACCESS
URL https://www.ijper.org/sites/default/files/IndJPhaEdRes-56-3-789.pdf
Link text Click here
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Source of classification or shelving scheme
Koha item type Articles Abstract Database
Holdings
Withdrawn status Lost status Source of classification or shelving scheme Damaged status Not for loan Permanent Location Current Location Shelving location Date acquired Barcode Date last seen Price effective from Koha item type
          School of Pharmacy School of Pharmacy Archieval Section 2022-08-26 2022-1389 2022-08-26 2022-08-26 Articles Abstract Database
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