Khalid Mehmood’s research while affiliated with Islamia University of Bahawalpur and other places

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Publications (1)


Cell viability (%) after the exposure of the series of concentration of ivermectin
X-axis showing the concentration of ivermectin and y-axis representing the Cell viability (%). Different alphabets showing the level of significance (p≤0.05).
DNA damage findings after the exposure of Ivermectin
x-axis showing the concentration of ivermectin and y-axis representing the DNA damage. Different alphabets showing the level of significance (p≤0.05).
A. Comet formation observed under fluorescent microscope in MDBK cell line (Left side). B. Formation of Micronuclei in MDBK cell line (Right side). Scale bar 20 um.
Micronuclei formation along with different doses of IVM concentration
x-axis showing the concentration of ivermectin and y-axis representing the DNA damage. Different alphabets showing the level of significance (p≤0.05).
Gene expression of OGG1 and HPRT1 gene between control and treated samples

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Evaluation of genotoxic effect via expression of DNA damage responsive gene induced by ivermectin on MDBK cell line
  • Article
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May 2024

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2 Citations

Muhammad Muddassir Ali

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Zainab Farhad

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Khalid Mehmood

Ivermectin (IVM) is an anti-parasitic drug which is used for treating parasitic infestations. It has been used in humans for treating intestinal strongyloidiasis and onchocerciasis however, currently researchers are investigating its potential for treating coronavirus SARS-CoV-2. Due to its broad-spectrum activities, IVM is being used excessively in animals which has generated an interest for researchers to investigate its toxic effects. Cytotoxic and genotoxic effects have been reported in animals due to excessive usage of IVM. Therefore, this study aims to evaluate the cytotoxic and genotoxic effects of IVM on the Madin-Darby-Bovine-Kidney (MDBK) cell line by examining the expression of a DNA damage-responsive gene (OGG1). Cytotoxicity of IVM was tested using an assay (MTT 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide), whereas the genotoxicity was evaluated using comet assay along with micronucleus assay. Moreover, the gene expression of DNA damage response gene (OGG1) was measured by qRT-PCR, after extraction of RNA from the MDBK cell line using the TRIzol method and its conversion to cDNA by reverse-transcriptase PCR. During the experiment, cell viability percentage was measured at different doses of IVM i.e., 25%, 50%, 75%, along with LC50/2, LC50 and LC50*2. It was observed that the gene expression of OGG1 increased as the concentration of IVM increased. It was concluded that IVM has both cytotoxic and genotoxic effects on the MDBK cell line. Furthermore, it is recommended that studies related to the toxic effects of IVM at molecular level and on other model organisms should be conducted to combat its hazardous effects.

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Citations (1)


... Numerous xenobiotics can lead to genotoxic effects via direct DNA damage, indirect DNA damage, and epigenetic changes (Han et al., 2018;Ambreen et al., 2023;Al-Saeed et al., 2023;Ali et al., 2024). Several studies have assessed neonicotinoid genotoxicity by examining chromosomal aberrations (CAs), sister chromatid exchanges (SCEs), comet assays, and micronucleus tests (MN) in vitro and in vivo (Han et al., 2018). ...

Reference:

FUCOIDAN FROM Fucus vesiculosus, REGULATES OXIDATIVE AND TRANSCRIPTIONAL RESPONSES IN THE SULFOXAFLOR EXPOSED MICE LIVER: ASSESMENT OF DNA DAMAGE GENES, THAT REPAIR DNA DAMAGE (XRCC1, OGG1, APE1, AND PARP1), AND THE ANTIOXIDANT STATUS
Evaluation of genotoxic effect via expression of DNA damage responsive gene induced by ivermectin on MDBK cell line