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Ifanosine: Olea europaea L. and Hyphaene thebaica L. combination, from traditional utilization to rational formulation: Preclinical and clinical efficacy on hypertensives patients.
Zakraoui, Mariem; Outman, Ahlam; Kinambamba, Milène Simone; Bouhrim, Mohamed; Ndjib, Rosette Christelle; Al Kamaly, Omkulthom; Alshawwa, Samar Zuhair; Seid, Abakar Bechir; Cordier, Janine; Ngoupayo, Joseph; Longo-Mbenza, Benjamin; Gressier, Bernard; Parvez, Mohammad Khalid; Paskovic, Igor; Hamrouni, Lamia; Eto, Bruno.
Afiliação
  • Zakraoui M; Laboratories TBC, Laboratory of Pharmacology, Pharmacokinetics and Clinical Pharmacy, Faculty of Phamacy, University of Lille, 3, rue du Professeur Laguesse, B.P. 83, F-59000, Lille, France; Faculty of Sciences of Tunis, University of Tunis El Manar, 2092, Tunis, Tunisia; Laboratory for the Manageme
  • Outman A; Laboratories TBC, Laboratory of Pharmacology, Pharmacokinetics and Clinical Pharmacy, Faculty of Phamacy, University of Lille, 3, rue du Professeur Laguesse, B.P. 83, F-59000, Lille, France. Electronic address: ahlam.outman.etu@univ-lille.fr.
  • Kinambamba MS; Laboratories TBC, Laboratory of Pharmacology, Pharmacokinetics and Clinical Pharmacy, Faculty of Phamacy, University of Lille, 3, rue du Professeur Laguesse, B.P. 83, F-59000, Lille, France. Electronic address: milenas242008@hotmail.com.
  • Bouhrim M; Laboratories TBC, Laboratory of Pharmacology, Pharmacokinetics and Clinical Pharmacy, Faculty of Phamacy, University of Lille, 3, rue du Professeur Laguesse, B.P. 83, F-59000, Lille, France; Laboratory of Biological Engineering, Team of Functional and Pathological Biology, Faculty of Sciences and Te
  • Ndjib RC; Laboratories TBC, Laboratory of Pharmacology, Pharmacokinetics and Clinical Pharmacy, Faculty of Phamacy, University of Lille, 3, rue du Professeur Laguesse, B.P. 83, F-59000, Lille, France; Laboratory of Botany and Traditional Medicine, Institute of Medical research and Medicinal Plants Studies, B0
  • Al Kamaly O; Department of Pharmaceutical Sciences, College of Pharmacy, Princess Nourah Bint Abdulrahman University, P.O. Box 84428, Riyadh, 11671, Saudi Arabia. Electronic address: omalkmali@pnu.edu.sa.
  • Alshawwa SZ; Department of Pharmaceutical Sciences, College of Pharmacy, Princess Nourah Bint Abdulrahman University, P.O. Box 84428, Riyadh, 11671, Saudi Arabia. Electronic address: SZAlshawwa@pnu.edu.sa.
  • Seid AB; Direction of Pharmacopeia and Traditional Medicine, Ministry of Health and Prevention, B.P. 440, N'djamena, Chad; Faculty of Medicine and Biomedical Sciences, University of Yaoundé 1, Bo 1634, Yaoundé, Cameroon. Electronic address: seidabakaraldahby@yahoo.fr.
  • Cordier J; Chad-China Friendship Hospital Center, N'djamena. Chad, Chad. Electronic address: cordier@laboratoire-tbc.com.
  • Ngoupayo J; Faculty of Medicine and Biomedical Sciences, University of Yaoundé 1, Bo 1634, Yaoundé, Cameroon. Electronic address: ngoupayo@gmail.com.
  • Longo-Mbenza B; Faculty of Medicine, The University of Kinshasa, Democratic Republic of Congo and LOMO University for research, LIMETE, RDC, Kinshasa, Congo. Electronic address: longombenza@gmail.com.
  • Gressier B; Laboratory of Pharmacology, Pharmacokinetics and Clinical Pharmacy, University of Lille, Faculty of Pharmacy, 3, rue du Professeur Laguesse, B.P. 83, F-59000, Lille, France. Electronic address: bernard.gressier@univ-lille.fr.
  • Parvez MK; Department of Pharmacognosy, College of Pharmacy King Saud University, Riyadh, Saudi Arabia. Electronic address: mohkhalid@ksu.edu.sa.
  • Paskovic I; Department of Agriculture and Nutrition, Institute of Agriculture and Tourism, Karla Huguesa 8, 52440, Porec, Croatia. Electronic address: paskovic@iptpo.hr.
  • Hamrouni L; Laboratory for the Management and development of Forest resources INRGREF, University of Carthage, Tunisia. Electronic address: hamrounilam@yahoo.fr.
  • Eto B; Laboratories TBC, Laboratory of Pharmacology, Pharmacokinetics and Clinical Pharmacy, Faculty of Phamacy, University of Lille, 3, rue du Professeur Laguesse, B.P. 83, F-59000, Lille, France. Electronic address: etobr@laboratoires-tbc.com.
J Ethnopharmacol ; 325: 117834, 2024 May 10.
Article em En | MEDLINE | ID: mdl-38309486
ABSTRACT
ETHNOPHARMACOLOGICAL RELEVANCE Olea europaea L. and Hyphaene thebaica L. are commonly employed by traditional healers in Africa for treating and preventing hypertension, either individually or in a polyherbal preparation (Ifanosine). AIM OF THE STUDY The primary aim was to assess the antihypertensive effects of Olea europaea L. leaves aqueous extract (OEL), Hyphaene thebaica L. mesocarp extract (HT), and the Ifanosine on isolated rat aorta rings. The secondary objective was to evaluate the clinical benefits of a new oral formulation of Ifanosine. MATERIALS AND

METHODS:

In vitro studies using an isometric transducer examined the antihypertensive effects of HT, OEL, and Ifanosine on rat aorta. Ussing chambers technic were employed to measure mucosal to serosal fluxes and total transepithelial electrical conductance (Gt) to assess the intestinal bioavailability of HT, OEL, and Ifanosine. HPLC was utilized to determine the phytochemical composition of OEL and HT extracts. Subchronic toxicity investigations involved two groups of rats, treated with either water (control) or Ifanosine at 5 g/kg for 28 days. Clinical benefits of the new Ifanosine formulation were evaluated in an observational study with 32 hypertensive patients receiving a fixed oral dose of 3.5 mg three times a day for 30 days.

RESULTS:

Aqueous extracts induced dose-dependent relaxation of rat aorta rings, with HT and OEL having higher IC50 values than Ifanosine (IC50 = 44.76 ± 1.35 ng/mL, 58.67 ± 1.02 ng/mL, and 29.46 ± 0.26 ng/mL, respectively). The pA2 values of OEL and HT were 1 and 0.6, respectively, while Ifanosine was 0.06. Intestinal bioavailability studies revealed better Prazosin bioavailability than plant extracts. Toxicological studies demonstrated the safety of Ifanosine, supported by histological examinations and biochemical parameters in rat blood. Biochemical analyses indicated flavonoids and phenolic acids as dominant active constituents. Clinical benefits in humans included reduced SBP, DBP, LDL-c, VLDL-c, and TAG, and increased HDL-c without overt adverse effects.

CONCLUSION:

This study validates the traditional use of OEL and HT for hypertension and advocates for alternative and combinatorial polyphytotherapy (ACP) to enhance traditional remedies.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Olea / Hipertensão Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Olea / Hipertensão Idioma: En Ano de publicação: 2024 Tipo de documento: Article