Changes in Pharmacokinetics and Pharmacodynamics of Losartan in Experimental Diseased Rats Treated with <i>Curcuma longa</i> and <i>Lepidium sativum</i>

The current study investigated “pharmacodynamics and pharmacokinetics interactions” of losartan with <i>Curcuma longa</i> (CUR) and <i>Lepidium sativum</i> (LS) in hypertensive rats. Hypertension was induced by oral administration of L-NAME (40 mg/kg) for two weeks. Oral admi...

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Main Authors: Abdul Ahad, Mohammad Raish, Ibrahim Abdelsalam Abdelrahman, Yousef A. Bin Jardan, Mohd Aftab Alam, Abdullah M. Al-Mohizea, Fahad I. Al-Jenoobi
Format: Article
Language:English
Published: MDPI AG 2022-12-01
Series:Pharmaceuticals
Subjects:
Online Access:https://www.mdpi.com/1424-8247/16/1/33
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author Abdul Ahad
Mohammad Raish
Ibrahim Abdelsalam Abdelrahman
Yousef A. Bin Jardan
Mohd Aftab Alam
Abdullah M. Al-Mohizea
Fahad I. Al-Jenoobi
author_facet Abdul Ahad
Mohammad Raish
Ibrahim Abdelsalam Abdelrahman
Yousef A. Bin Jardan
Mohd Aftab Alam
Abdullah M. Al-Mohizea
Fahad I. Al-Jenoobi
author_sort Abdul Ahad
collection DOAJ
description The current study investigated “pharmacodynamics and pharmacokinetics interactions” of losartan with <i>Curcuma longa</i> (CUR) and <i>Lepidium sativum</i> (LS) in hypertensive rats. Hypertension was induced by oral administration of L-NAME (40 mg/kg) for two weeks. Oral administration of CUR or LS shows some substantial antihypertensive activity. The systolic blood pressure (SBP) of hypertensive rats was decreased by 7.04% and 8.78% 12 h after treatment with CUR and LS, respectively, as compared to rats treated with L-NAME alone. LS and CUR display the ability to potentiate the blood pressure-lowering effects of losartan in hypertensive rats. A greater decrease in SBP, by 11.66% and 13.74%, was observed in hypertensive rats treated with CUR + losartan and LS + losartan, respectively. Further, both the investigated herbs, CUR and LS, caused an increase in plasma concentrations of losartan in hypertensive rats. The AUC<sub>0-t</sub>, AUC<sub>0-inf</sub> and AUMC<sub>0-inf</sub> of losartan were increased by 1.25-fold, 1.28-fold and 1.09-fold in hypertensive rats treated with CUR + losartan. A significant (<i>p</i> < 0.05) increase in AUC<sub>0-t</sub> (2.41-fold), AUC<sub>0-inf</sub> (3.86-fold) and AUMC<sub>0-inf</sub> (8.35-fold) of losartan was observed in hypertensive rats treated with LS + losartan. The present study affirms that interactions between CUR or LS with losartan alter both “pharmacokinetics and pharmacodynamics” of the drug. Concurrent administration of losartan with either CUR or LS would require dose adjustment and intermittent blood pressure monitoring for clinical use in hypertensive patients. Additional investigation is necessary to determine the importance of these interactions in humans and to elucidate the mechanisms of action behind these interactions.
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spelling doaj.art-712af78b788b410bb66c3f7a2b8a7b6d2023-11-30T23:54:50ZengMDPI AGPharmaceuticals1424-82472022-12-011613310.3390/ph16010033Changes in Pharmacokinetics and Pharmacodynamics of Losartan in Experimental Diseased Rats Treated with <i>Curcuma longa</i> and <i>Lepidium sativum</i>Abdul Ahad0Mohammad Raish1Ibrahim Abdelsalam Abdelrahman2Yousef A. Bin Jardan3Mohd Aftab Alam4Abdullah M. Al-Mohizea5Fahad I. Al-Jenoobi6Department of Pharmaceutics, College of Pharmacy, King Saud University, Riyadh 11451, Saudi ArabiaDepartment of Pharmaceutics, College of Pharmacy, King Saud University, Riyadh 11451, Saudi ArabiaDepartment of Pharmaceutics, College of Pharmacy, King Saud University, Riyadh 11451, Saudi ArabiaDepartment of Pharmaceutics, College of Pharmacy, King Saud University, Riyadh 11451, Saudi ArabiaDepartment of Pharmaceutics, College of Pharmacy, King Saud University, Riyadh 11451, Saudi ArabiaDepartment of Pharmaceutics, College of Pharmacy, King Saud University, Riyadh 11451, Saudi ArabiaDepartment of Pharmaceutics, College of Pharmacy, King Saud University, Riyadh 11451, Saudi ArabiaThe current study investigated “pharmacodynamics and pharmacokinetics interactions” of losartan with <i>Curcuma longa</i> (CUR) and <i>Lepidium sativum</i> (LS) in hypertensive rats. Hypertension was induced by oral administration of L-NAME (40 mg/kg) for two weeks. Oral administration of CUR or LS shows some substantial antihypertensive activity. The systolic blood pressure (SBP) of hypertensive rats was decreased by 7.04% and 8.78% 12 h after treatment with CUR and LS, respectively, as compared to rats treated with L-NAME alone. LS and CUR display the ability to potentiate the blood pressure-lowering effects of losartan in hypertensive rats. A greater decrease in SBP, by 11.66% and 13.74%, was observed in hypertensive rats treated with CUR + losartan and LS + losartan, respectively. Further, both the investigated herbs, CUR and LS, caused an increase in plasma concentrations of losartan in hypertensive rats. The AUC<sub>0-t</sub>, AUC<sub>0-inf</sub> and AUMC<sub>0-inf</sub> of losartan were increased by 1.25-fold, 1.28-fold and 1.09-fold in hypertensive rats treated with CUR + losartan. A significant (<i>p</i> < 0.05) increase in AUC<sub>0-t</sub> (2.41-fold), AUC<sub>0-inf</sub> (3.86-fold) and AUMC<sub>0-inf</sub> (8.35-fold) of losartan was observed in hypertensive rats treated with LS + losartan. The present study affirms that interactions between CUR or LS with losartan alter both “pharmacokinetics and pharmacodynamics” of the drug. Concurrent administration of losartan with either CUR or LS would require dose adjustment and intermittent blood pressure monitoring for clinical use in hypertensive patients. Additional investigation is necessary to determine the importance of these interactions in humans and to elucidate the mechanisms of action behind these interactions.https://www.mdpi.com/1424-8247/16/1/33garden cressherb–drug interactionhypertensionL-NAMElosartanpharmacodynamic
spellingShingle Abdul Ahad
Mohammad Raish
Ibrahim Abdelsalam Abdelrahman
Yousef A. Bin Jardan
Mohd Aftab Alam
Abdullah M. Al-Mohizea
Fahad I. Al-Jenoobi
Changes in Pharmacokinetics and Pharmacodynamics of Losartan in Experimental Diseased Rats Treated with <i>Curcuma longa</i> and <i>Lepidium sativum</i>
Pharmaceuticals
garden cress
herb–drug interaction
hypertension
L-NAME
losartan
pharmacodynamic
title Changes in Pharmacokinetics and Pharmacodynamics of Losartan in Experimental Diseased Rats Treated with <i>Curcuma longa</i> and <i>Lepidium sativum</i>
title_full Changes in Pharmacokinetics and Pharmacodynamics of Losartan in Experimental Diseased Rats Treated with <i>Curcuma longa</i> and <i>Lepidium sativum</i>
title_fullStr Changes in Pharmacokinetics and Pharmacodynamics of Losartan in Experimental Diseased Rats Treated with <i>Curcuma longa</i> and <i>Lepidium sativum</i>
title_full_unstemmed Changes in Pharmacokinetics and Pharmacodynamics of Losartan in Experimental Diseased Rats Treated with <i>Curcuma longa</i> and <i>Lepidium sativum</i>
title_short Changes in Pharmacokinetics and Pharmacodynamics of Losartan in Experimental Diseased Rats Treated with <i>Curcuma longa</i> and <i>Lepidium sativum</i>
title_sort changes in pharmacokinetics and pharmacodynamics of losartan in experimental diseased rats treated with i curcuma longa i and i lepidium sativum i
topic garden cress
herb–drug interaction
hypertension
L-NAME
losartan
pharmacodynamic
url https://www.mdpi.com/1424-8247/16/1/33
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