Evidence map›Paper›PMID 39966363›Full record

ArticleCardiovascular & hematological disorders drug targets2025

Vasorelaxant and Antihypertensive Effects of Extracts from the Leaves of

Gabriela Perez-Barron, Samuel Estrada-Soto, Rafael Villalobos-Molina, Luis Arias-Duran, Jaime Escalante-Garcia, Irene Perea-Arango, Rogelio Hernandez-Pando

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Article in Cardiovascular & hematological disorders drug targets, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Gabriela Perez-BarronUnidad de Biomedicina, Facultad de Estudios Superiores Iztacala, Universidad Nacional Autónoma de México, Av. de los Barrios 1, Hab los Reyes de Ixtacala, C.P. 54090, Tlalnepantla, Estado de México, México.ORCID 0000-0002-7579-8278
Samuel Estrada-SotoFacultad de Farmacia, Universidad Autónoma del Estado de Morelos, Av. Universidad 1001, Col. Chamilpa, C.P. 62209, Cuernavaca, Morelos, México.ORCID 0000-0003-1860-0744
Rafael Villalobos-MolinaUnidad de Biomedicina, Facultad de Estudios Superiores Iztacala, Universidad Nacional Autónoma de México, Av. de los Barrios 1, Hab los Reyes de Ixtacala, C.P. 54090, Tlalnepantla, Estado de México, México.ORCID 0000-0001-5472-7713
Luis Arias-DuranFacultad de Farmacia, Universidad Autónoma del Estado de Morelos, Av. Universidad 1001, Col. Chamilpa, C.P. 62209, Cuernavaca, Morelos, México.ORCID 0000-0002-7258-7088
Jaime Escalante-GarciaCentro de Investigaciones Químicas, Universidad Autónoma del Estado de Morelos, Av. Universidad 1001, Col. Chamilpa, C.P. 62209, Cuernavaca, Morelos, México.ORCID 0000-0001-5485-0244
Irene Perea-ArangoCentro de Investigación en Biotecnología, Universidad Autónoma del Estado de Morelos, Av. Universidad 1001, Col. Chamilpa, C.P. 62209, Cuernavaca, Morelos, México.ORCID 0000-0003-1944-4739
Rogelio Hernandez-PandoUnidad de Patología Experimental, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zuribán, Vasco de Quiroga 15, Belisario Domínguez Secc. 16, Tlalpan, C.P. 14080, Ciudad de México, México.ORCID 0000-0003-1292-3833

Funding

CONAHCYT FORDECYT-PRONACES 377882/2020PAPIIT, DGAPA, UNAM IN210222
6 · The paper itself

Abstract

backgroundCasimiroa edulis La Llave (Rutaceae), commonly known as "zapote blanco", is a tree widely distributed in Mexico's tropical and subtropical areas. The decoction of its leaves is traditionally used as a natural remedy to treat hypertension and anxiety.

objectivesThe present study aimed to determine the vasorelaxant and antihypertensive effects of C. edulis extracts and evaluate the acute and sub-acute toxicity of one of the most active extracts.

methodsThe hydro-alcohol and organic (hexane, dichloromethane, and methanol) extracts, obtained from the leaves of C. edulis, were evaluated on isolated aorta rat rings in the presence and absence of endothelium to determine their vasorelaxant effect. Then, most active extracts were studied to evaluate the functional mechanism of their vasorelaxant action and antihypertensive effect on spontaneously hypertensive rats (SHR). The acute and sub-acute toxicity of dichloromethane extract was evaluated following the OECD 423 and 407 protocols.

resultsThe hexane (HE) and dichloromethane (DE) extracts from Casimiroa edulis induced significant vasorelaxant action on isolated rat aortic rings with (Emax 104.7 ± 1.4% and Emax 97.3 ± 6.7%, respectively) and without (Emax 94.9 ± 3.5% and Emax 67.4 ± 1.0%, respectively) endothelium, and this effect was partially endothelium-dependent. Their vasorelaxant action was modified by L-NAME (nitric oxide synthase inhibitor) and ODQ (soluble guanylyl cyclase inhibitor); however, indomethacin did not modify the effect. Also, both HE and DE significantly decreased the contraction induced by KCl in a concentration-dependent manner and the maximal effect induced by CaCl2. Moreover, DE showed a significant decrease in systolic and diastolic blood pressure in SHR at 7 hours and 15 days after treatment, respectively. Finally, the toxicity test of DE allowed classifying it in category 5, indicating it to be a non-toxic extract based on OECD guideline 423; the LD50 value was estimated to be greater than 2,000 mg/Kg and smaller than 5,000 mg/Kg in Wistar rats.

conclusionThe results demonstrated hexane and dichloromethane extracts to exert a vasorelaxant effect through endothelium-dependent NO release and cGMP increase, as well as by calcium channel blockade. Also, dichloromethane extract showed efficacy and security as a potential antihypertensive agent.

Indexed as

Antihypertensive AgentsCalcium Channel BlockersNitric OxidePlant ExtractsPlant LeavesRutaceaeVasodilator AgentsAnimalsHypertensionMaleRatsRats, Inbred SHRRats, WistarAntihypertensive AgentsCalcium Channel BlockersNitric OxidePlant ExtractsVasodilator Agentsantihypertensivecalcium channels blockadeCasimiroa edulisnitric oxidetoxicity.vasorelaxation

Identifiers

PMID39966363

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.