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Kalanchoe crenata Andrews (Haw.) Improves Losartan’s Antihypertensive Activity

dc.contributor.authorAmatto, Pedro de Padua G.
dc.contributor.authorCoppede, Juliana da Silva
dc.contributor.authorKitanishi, Carla Renata
dc.contributor.authorBraga, Giovana Graça
dc.contributor.authorFaria, Thaysa Carvalho de
dc.contributor.authorRizzi, Elen
dc.contributor.authorFrança, Suzelei de Castro
dc.contributor.authorBasso, Fernanda [UNESP]
dc.contributor.authorLopes, Adriana Aparecida
dc.contributor.authorCarmona, Fábio
dc.contributor.authorContini, Silvia Helena Taleb
dc.contributor.authorPereira, Ana Maria Soares
dc.contributor.institutionUniversity of Ribeirão Preto
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.contributor.institutionBotanical Garden of Medicinal Plants Ordem e Progresso
dc.date.accessioned2025-04-29T20:07:11Z
dc.date.issued2024-12-01
dc.description.abstractBackground: Cardiovascular diseases constitute one of the leading causes of morbidity and mortality worldwide. Herbal medicines represent viable alternatives to the synthetic drugs currently employed in the control of hypertension. This study aimed to isolate and identify the chemical markers of Kalanchoe crenata and to investigate the antihypertensive and anti-matrix metalloproteinase (MMP2) activities of an aqueous extract of the leaves. Methods: The main constituents of the aqueous extract of K. crenata were separated by ultra-performance liquid chromatography–mass spectrometry, and their presence was identified by NMR spectroscopy. Renovascular hypertension was induced in male Wistar rats using the two-kidney one-clip method (HTN groups), while control animals (Sham groups) were submitted to Sham surgery. Six groups of 10 animals each were treated daily for eight weeks as follows: Sham 1 (carrier), Sham 2 (K. crenata extract), HTN.1 (carrier), HTN.2 (K. crenata extract), HTN 3 (losartan), and HTN 4 (K. crenata extract with losartan). Results: The main compounds of the extract were patuletin 3-O-(4″-O-acetyl-α-L-rhamnopyranosyl)-7-O-(3‴-O-acetyl-α-L-rhamnopyranoside) (1), patuletin 3-O-α-L-rhamnopyranosyl-7-O-L-rhamnopyranoside (2), and trans-caffeoyl-malic acid (3), with compounds 1 and 2 being chemical markers of the species. Significant reductions (p < 0.05) in systolic blood pressure and MMP2 (72kDa isoform) activity were observed in the HTN 4 group. Conclusions: The association of K. crenata extract and losartan presented in vivo effects against hypertension.en
dc.description.affiliationDepartment of Biotechnology of Medicinal Plants University of Ribeirão Preto
dc.description.affiliationSchool of Dentistry São Paulo State University Júlio de Mesquita Filho
dc.description.affiliationRibeirão Preto Medical School University of São Paulo
dc.description.affiliationBotanical Garden of Medicinal Plants Ordem e Progresso
dc.description.affiliationUnespSchool of Dentistry São Paulo State University Júlio de Mesquita Filho
dc.identifierhttp://dx.doi.org/10.3390/molecules29246010
dc.identifier.citationMolecules, v. 29, n. 24, 2024.
dc.identifier.doi10.3390/molecules29246010
dc.identifier.issn1420-3049
dc.identifier.scopus2-s2.0-85213251636
dc.identifier.urihttps://hdl.handle.net/11449/306808
dc.language.isoeng
dc.relation.ispartofMolecules
dc.sourceScopus
dc.subjecthypertension
dc.subjectmedicinal plant
dc.subjectmurine model
dc.subjectpatuletins
dc.subjectsystolic blood pressure
dc.titleKalanchoe crenata Andrews (Haw.) Improves Losartan’s Antihypertensive Activitypt
dc.typeArtigopt
dspace.entity.typePublication
unesp.author.orcid0000-0003-2229-038X[1]
unesp.author.orcid0000-0002-4197-9927[2]
unesp.author.orcid0009-0008-2046-7261[3]
unesp.author.orcid0000-0002-3823-8845[6]
unesp.author.orcid0000-0003-4864-430X[7]
unesp.author.orcid0000-0002-7170-2371[8]
unesp.author.orcid0000-0003-1107-2547[9]
unesp.author.orcid0000-0001-5743-0325[10]
unesp.author.orcid0000-0003-3817-9782[11]
unesp.author.orcid0000-0002-3478-4718[12]

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