Effect of Alcohol Consumption during Antiretroviral Therapy on HIV-1 Replication: Role of Cytochrome P3A4 Enzyme
Alcohol consumption is prevalent in HIV/AIDS infected patients. It possesses serious effects on protease inhibitors (PIs), which are used as an antiviral drug. While taking PIs, the secretion of Cytochrome P3A4 (CYP3A4) enzymes occurs from the liver and it metabolizes the drug to CYP3A4-PI complex....
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doaj-25d0266358a9447db169a13a246943542020-11-25T02:19:09ZengInternational Journal of Mathematical, Engineering and Management SciencesInternational Journal of Mathematical, Engineering and Management Sciences2455-77492455-77492019-08-014492293510.33889/IJMEMS.2019.4.4-073Effect of Alcohol Consumption during Antiretroviral Therapy on HIV-1 Replication: Role of Cytochrome P3A4 EnzymeSrijita Mondal0Priyanka Ghosh1Dibyendu Biswas2Priti Kumar Roy3Centre for Mathematical Biology and Ecology, Department of Mathematics, Jadavpur University, Kolkata - 700032, IndiaCentre for Mathematical Biology and Ecology, Department of Mathematics, Jadavpur University, Kolkata - 700032, IndiaDepartment of Mathematics, City College of Commerce and Business Administration, 13, Surya Sen Street, Kolkata-700012, IndiaCentre for Mathematical Biology and Ecology, Department of Mathematics, Jadavpur University, Kolkata - 700032, IndiaAlcohol consumption is prevalent in HIV/AIDS infected patients. It possesses serious effects on protease inhibitors (PIs), which are used as an antiviral drug. While taking PIs, the secretion of Cytochrome P3A4 (CYP3A4) enzymes occurs from the liver and it metabolizes the drug to CYP3A4-PI complex. Alcohol consumption increases the rate of metabolism of PIs. In this research article, we have formulated a set of nonlinear differential equations based on the enzymatic activity of CYP3A4 for alcoholic HIV infected patients. Here, we have analytically compared the dynamics of PIs metabolism between alcoholic and non-alcoholic HIV infected patients and also investigated how the infection is being accelerated by enhancing viral load due to alcohol consumption. Finally, our analytical results are verified by numerical findings.https://www.ijmems.in/assets//73-IJMEMS-BM-08-Vol.%204,%20No.%204,%20922%E2%80%93935,%202019.pdfHIV/AIDSViral loadAlcohol consumptionCYP3A4 enzymeProtease inhibitor |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Srijita Mondal Priyanka Ghosh Dibyendu Biswas Priti Kumar Roy |
spellingShingle |
Srijita Mondal Priyanka Ghosh Dibyendu Biswas Priti Kumar Roy Effect of Alcohol Consumption during Antiretroviral Therapy on HIV-1 Replication: Role of Cytochrome P3A4 Enzyme International Journal of Mathematical, Engineering and Management Sciences HIV/AIDS Viral load Alcohol consumption CYP3A4 enzyme Protease inhibitor |
author_facet |
Srijita Mondal Priyanka Ghosh Dibyendu Biswas Priti Kumar Roy |
author_sort |
Srijita Mondal |
title |
Effect of Alcohol Consumption during Antiretroviral Therapy on HIV-1 Replication: Role of Cytochrome P3A4 Enzyme |
title_short |
Effect of Alcohol Consumption during Antiretroviral Therapy on HIV-1 Replication: Role of Cytochrome P3A4 Enzyme |
title_full |
Effect of Alcohol Consumption during Antiretroviral Therapy on HIV-1 Replication: Role of Cytochrome P3A4 Enzyme |
title_fullStr |
Effect of Alcohol Consumption during Antiretroviral Therapy on HIV-1 Replication: Role of Cytochrome P3A4 Enzyme |
title_full_unstemmed |
Effect of Alcohol Consumption during Antiretroviral Therapy on HIV-1 Replication: Role of Cytochrome P3A4 Enzyme |
title_sort |
effect of alcohol consumption during antiretroviral therapy on hiv-1 replication: role of cytochrome p3a4 enzyme |
publisher |
International Journal of Mathematical, Engineering and Management Sciences |
series |
International Journal of Mathematical, Engineering and Management Sciences |
issn |
2455-7749 2455-7749 |
publishDate |
2019-08-01 |
description |
Alcohol consumption is prevalent in HIV/AIDS infected patients. It possesses serious effects on protease inhibitors (PIs), which are used as an antiviral drug. While taking PIs, the secretion of Cytochrome P3A4 (CYP3A4) enzymes occurs from the liver and it metabolizes the drug to CYP3A4-PI complex. Alcohol consumption increases the rate of metabolism of PIs. In this research article, we have formulated a set of nonlinear differential equations based on the enzymatic activity of CYP3A4 for alcoholic HIV infected patients. Here, we have analytically compared the dynamics of PIs metabolism between alcoholic and non-alcoholic HIV infected patients and also investigated how the infection is being accelerated by enhancing viral load due to alcohol consumption. Finally, our analytical results are verified by numerical findings. |
topic |
HIV/AIDS Viral load Alcohol consumption CYP3A4 enzyme Protease inhibitor |
url |
https://www.ijmems.in/assets//73-IJMEMS-BM-08-Vol.%204,%20No.%204,%20922%E2%80%93935,%202019.pdf |
work_keys_str_mv |
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1724878209266221056 |