Publication:
Effect of myrtus communis extract on serum cytokines in angiotensin dependent_x000D_ hypertensive rats

dc.contributor.authorsZatiye ÇEVİKELLİ;Büşra ERTAŞ;ALİ ŞEN;Göksel ŞENER
dc.date.accessioned2022-03-15T16:59:45Z
dc.date.accessioned2026-01-11T10:24:42Z
dc.date.available2022-03-15T16:59:45Z
dc.date.issued2020
dc.description.abstractIn angiotensin dependent hypertension, high blood pressure and elevated angiotensin 2 levels lead to inflammation by increasing the pro-inflammatory cytokine levels.Since Myrtus communis have showed anti-inflammatory acvtivity in ethnobotanical researches and experimental studies, we investigated the effect of Myrtus communisextract against inflammation in a rat model of angiotensin dependent hypertension. Wistar albino rats were divided as sham-operated control, RVH and Myrtus communisextract-treated RVH groups. Left renal arteries of the rats were implanted with silver clip. Indirect blood pressure measurement of rats was provided with tail-cuff methodbefore the surgery, 3 and 9 weeks after the surgery. Myrtus communis extract (100 mg/kg, orally) or vehicle was administered for 6 weeks. At the end of the study, serumsamples were collected to investigate tumor necrosis alpha (TNF-α), interleukin-1 beta (IL-1β) and IL-6 levels. RVH resulted in significant increases in these proinflammatorycytokine levels. In the Myrtus communis extract treatment group, this increasement was abolished. The present data demonstrated that Myrtus communis attenuatesRVH-induced inflammation.
dc.identifier.doi10.5455/medscience.2019.08.9204
dc.identifier.issn2147-0634;2147-0634
dc.identifier.urihttps://hdl.handle.net/11424/253517
dc.language.isoeng
dc.relation.ispartofMedicine Science
dc.rightsinfo:eu-repo/semantics/openAccess
dc.titleEffect of myrtus communis extract on serum cytokines in angiotensin dependent_x000D_ hypertensive rats
dc.typearticle
dspace.entity.typePublication
oaire.citation.endPage407
oaire.citation.issue2
oaire.citation.startPage404
oaire.citation.titleMedicine Science
oaire.citation.volume9

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