Antihypertensive Potential of Pistacia lentiscus var. Chia: Molecular Insights and Therapeutic Implications

Author:

Efentakis Panagiotis1,Symeonidi Lydia1,Gianniou Despoina D.2ORCID,Mikropoulou Eleni V.3ORCID,Giardoglou Panagiota4,Valakos Dimitrios5ORCID,Vatsellas Giannis6ORCID,Tsota Maria4ORCID,Kostomitsopoulos Nikolaos5ORCID,Smyrnioudis Ilias7ORCID,Trougakos Ioannis P.2ORCID,Halabalaki Maria3ORCID,Dedoussis Georgios V.4ORCID,Andreadou Ioanna1ORCID

Affiliation:

1. Laboratory of Pharmacology, Faculty of Pharmacy, National and Kapodistrian University of Athens, Panepistimiopolis, 15771 Zografou, Greece

2. Department of Cell Biology and Biophysics, Faculty of Biology, National and Kapodistrian University of Athens, 15784 Athens, Greece

3. Division of Pharmacognosy and Natural Products Chemistry, Department of Pharmacy, National and Kapodistrian University of Athens, 15771 Athens, Greece

4. Department of Nutrition and Dietetics, School of Health Science and Education, Harokopio University of Athens, 17671 Athens, Greece

5. Center of Basic Research, Biomedical Research Foundation of the Academy of Athens, 11527 Athens, Greece

6. Greek Genome Centre, Biomedical Research Foundation of the Academy of Athens, 11527 Athens, Greece

7. Mastiha Research Center, Seleperos Kallimasia, 82150 Chios, Greece

Abstract

Background: Hypertension poses a significant global health burden and is associated with cardiovascular morbidity. Chios mastic gum (CMG), derived from Pistacia lentiscus var. Chia, shows potential as a phytotherapeutic agent, due to its multifaceted beneficial effects. However, its anti-hypertensive effects and vascular, circulatory, and renal-related dysfunction, have not been thoroughly investigated. Herein, we aimed to explore the antihypertensive potential of CMG, focusing on vascular and renal endothelium, in vivo. Methods: Two models of hypertension in male rats, induced by Angiotensin II and Deoxycorticosterone acetate (DOCA)–high-salt administration, were utilized. CMG was administered at 220 mg/kg daily for four weeks after hypertension onset and blood pressure was measured non-invasively. Whole blood RNA sequencing, metabolomics, real-time PCR, and Western blot analyses of kidney and aorta tissues were additionally performed. Results: CMG significantly lowered systolic, diastolic, and mean blood pressure in both models. RNA sequencing revealed that CMG modulated immunity in the Angiotensin II model and metabolism in the DOCA–HS model. CMG downregulated genes related to oxidative stress and endothelial dysfunction and upregulated endothelial markers such as Vegfa. Metabolomic analysis indicated improved endothelial homeostasis via lysophosphatidylinositol upregulation. Conclusions: CMG emerges as a potent natural antihypertensive therapy, demonstrating beneficial effects on blood pressure and renal endothelial function.

Funder

European Union and the Operational Program for Competitiveness, Entrepreneurship and Innovation

Publisher

MDPI AG

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