Back to Search Start Over

Central nervous system, peripheral and hemodynamic effects of nanoformulated anandamide in hypertension.

Authors :
Martín Giménez VM
Mocayar Marón FJ
García S
Mazzei L
Guevara M
Yunes R
Manucha W
Source :
Advances in medical sciences [Adv Med Sci] 2021 Mar; Vol. 66 (1), pp. 72-80. Date of Electronic Publication: 2020 Dec 31.
Publication Year :
2021

Abstract

Purpose: Hypertensive lesions induce alterations at hemodynamic, peripheral, and central levels. Anandamide (N-arachidonoylethanolamine; AEA) protects neurons from inflammatory damage, but its free administration may cause central adverse effects. AEA controlled release by nanoformulations could reduce/eliminate its side effects. The present study aimed to evaluate the effects of nanoformulated AEA (nf-AEA) on systolic blood pressure (SBP), behavior, and central/peripheral inflammatory, oxidative, and apoptotic state in spontaneously hypertensive rats (SHR).<br />Materials/methods: Male rats were used, both Wistar Kyoto (WKY) and SHR (n ​= ​10 per group), with/without treatment with nf-AEA (obtained by electrospraying) at a weekly dose of 5 ​mg/kg IP for 4 weeks. SBP was measured and behavioral tests were performed. Inflammatory/oxidative markers were quantified at the central (brain cortex) and peripheral (serum) level.<br />Results: SHR showed hyperactivity, low anxiety, and high concentrations of central/peripheral inflammatory/oxidative markers, also higher apoptosis of brain cortical cells compared to WKY. As opposed to this group, treatment with nf-AEA in SHR significantly reduced SBP, peripheral/central inflammatory/oxidative makers, and central apoptosis. Nf-AEA also increased neuroprotective mechanisms mediated by intracellular heat shock protein 70 (Hsp70), which were attenuated in untreated SHR. Additionally, nf-AEA reversed the abnormal behaviors observed in SHR without producing central adverse effects.<br />Conclusions: Our results suggest protective properties of nf-AEA, both peripherally and centrally, through a signaling pathway that would involve the type I angiotensin II receptor, Wilms tumor transcription factor 1, Hsp70, and iNOS. Considering non-nf-AEA limitations, this nanoformulation could contribute to the development of new antihypertensive and behavioral disorder treatments associated with neuroinflammation.<br />Competing Interests: Declaration of competing interest The author(s) declare no potential conflicts of interest concerning the research, authorship, and/or publication of this article.<br /> (Copyright © 2020 Medical University of Bialystok. Published by Elsevier B.V. All rights reserved.)

Details

Language :
English
ISSN :
1898-4002
Volume :
66
Issue :
1
Database :
MEDLINE
Journal :
Advances in medical sciences
Publication Type :
Academic Journal
Accession number :
33388673
Full Text :
https://doi.org/10.1016/j.advms.2020.12.003