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Central nervous system, peripheral and hemodynamic effects of nanoformulated anandamide in hypertension.
- 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
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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.)
- Subjects :
- Animals
Antihypertensive Agents administration & dosage
Antihypertensive Agents chemistry
Arachidonic Acids administration & dosage
Arachidonic Acids chemistry
Blood Pressure
Endocannabinoids administration & dosage
Endocannabinoids chemistry
Hypertension metabolism
Hypertension pathology
Male
Nanoparticles administration & dosage
Oxidative Stress
Polyunsaturated Alkamides administration & dosage
Polyunsaturated Alkamides chemistry
Rats
Rats, Inbred SHR
Rats, Inbred WKY
Signal Transduction
Antihypertensive Agents pharmacology
Arachidonic Acids pharmacology
Central Nervous System drug effects
Endocannabinoids pharmacology
Hemodynamics
Hypertension drug therapy
Nanoparticles chemistry
Peripheral Nervous System drug effects
Polyunsaturated Alkamides pharmacology
Subjects
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