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Article

Metabolomic Profile, Plasmatic Levels of Losartan and EXP3174, Blood Pressure Control in Hypertensive Patients and Their Correlation with COVID-19

by
Kamila A. Queiroz
1,2,
Everton P. Vale
2,3,
Manuel Martín-Pastor
4,
Lílian G. S. Sólon
1,2 and
Francisco F. O. Sousa
1,2,3,*
1
Graduate Program on Pharmaceutical Sciences, Department of Biological & Health Sciences, Federal University of Amapa, Macapa 68903-419, Brazil
2
Laboratory of Quality Control, Bromatology and Microbiology, Department of Biological & Health Sciences, Federal University of Amapa, Macapa 68903-419, Brazil
3
Graduate Program on Pharmaceutical Innovation, Department of Biological & Health Sciences, Federal University of Amapa, Macapa 68903-419, Brazil
4
Unidade de Resonancia Magnetica, Área de Infraestruturas de Investigación, Campus Vida, Universidad de Santiago de Compostela, 15782 Santiago de Compostela, Spain
*
Author to whom correspondence should be addressed.
Pharmaceuticals 2023, 16(9), 1290; https://doi.org/10.3390/ph16091290
Submission received: 20 June 2023 / Revised: 21 July 2023 / Accepted: 27 July 2023 / Published: 13 September 2023
(This article belongs to the Special Issue Pharmacological Advances for Treatment in Hypertension)

Abstract

Systemic arterial hypertension (SAH) is one of the most prevalent chronic diseases worldwide and is related to serious health complications. It has been pointed out as a major risk factor for COVID-19. This study aimed to determine the impact of COVID-19 on the metabolomic profile, the correlation with the plasmatic levels of losartan and its active metabolite (EXP3174), biochemical markers, and blood pressure (BP) control in hypertensive patients. 1H NMR metabolomic profiles of hypertensive and normotensive patients with and without previous COVID-19 diagnosis were identified. Plasmatic levels of LOS and EXP3174 were correlated with BP, biochemical markers, and the metabolomic fingerprint of the groups. Biomarkers linked to important aspects of SAH and COVID-19 were identified, such as glucose, glutamine, arginine, creatinine, alanine, choline, erythritol, homogentisate, 0-tyrosine, and 2-hydroxybutyrate. Those metabolites are indicative of metabolic alterations, kidney damage, pulmonary dysfunction, and persistent inflammation, which can be found in both diseases. Some hypertensive patients did not reach the therapeutic levels of LOS and EXP3174, while the BP control was also limited among the normotensive patients with previous COVID-19 diagnoses. Metabolomics proved to be an important tool for assessing the effectiveness of losartan pharmacotherapy and the damage caused by SAH and COVID-19 in hypertensive patients.
Keywords: hypertension; COVID-19; metabolomics; losartan; EXP3174; plasmatic level hypertension; COVID-19; metabolomics; losartan; EXP3174; plasmatic level
Graphical Abstract

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MDPI and ACS Style

Queiroz, K.A.; Vale, E.P.; Martín-Pastor, M.; Sólon, L.G.S.; Sousa, F.F.O. Metabolomic Profile, Plasmatic Levels of Losartan and EXP3174, Blood Pressure Control in Hypertensive Patients and Their Correlation with COVID-19. Pharmaceuticals 2023, 16, 1290. https://doi.org/10.3390/ph16091290

AMA Style

Queiroz KA, Vale EP, Martín-Pastor M, Sólon LGS, Sousa FFO. Metabolomic Profile, Plasmatic Levels of Losartan and EXP3174, Blood Pressure Control in Hypertensive Patients and Their Correlation with COVID-19. Pharmaceuticals. 2023; 16(9):1290. https://doi.org/10.3390/ph16091290

Chicago/Turabian Style

Queiroz, Kamila A., Everton P. Vale, Manuel Martín-Pastor, Lílian G. S. Sólon, and Francisco F. O. Sousa. 2023. "Metabolomic Profile, Plasmatic Levels of Losartan and EXP3174, Blood Pressure Control in Hypertensive Patients and Their Correlation with COVID-19" Pharmaceuticals 16, no. 9: 1290. https://doi.org/10.3390/ph16091290

APA Style

Queiroz, K. A., Vale, E. P., Martín-Pastor, M., Sólon, L. G. S., & Sousa, F. F. O. (2023). Metabolomic Profile, Plasmatic Levels of Losartan and EXP3174, Blood Pressure Control in Hypertensive Patients and Their Correlation with COVID-19. Pharmaceuticals, 16(9), 1290. https://doi.org/10.3390/ph16091290

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