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Food and Chemical ToxicologyVolume 88, February 01, 2016, Pages 105-111

Curcumin attenuates Mancozeb-induced toxicity in rat thymocytes through mitochondrial survival pathway(Article)

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  • aInstitute of Physiology, Medical Faculty University of Nis, Bulevar Dr. Zorana Djindjica 81, Nis, 18000, Serbia
  • bMedical Faculty University of Nis, Bulevar Dr. Zorana Djindjica 81, Nis, Serbia
  • cInstitute for Treatment and Rehabilitation Niska Banja, Srpskih Junaka 2, Niska Banja, 18205, Serbia

Abstract

The widely used fungicide Mancozeb (Man) has been shown to cause genotoxic effects in rodents and toxicological manifestations in different cells, mainly by altering the antioxidant defense in cells. On the other hand, curcumin (Cur), a natural phenolic compound, is thought to possess anti-inflammatory and antioxidant properties. Here, we investigated the possible protective role of Cur on Man-induced toxicity in rat thymocytes and potential mechanism involved. Rat thymocytes were treated with Man(0.01 μg/ml) and/or increasing Cur(0.3, 1, 3 μM) concentrations and levels of cell viability, apoptosis, mitochondrial membrane potential (MMP),Bcl-2, Bax protein expression, caspase-3 and -9 activity and p38 MAPK signaling involvement were examined. Cells treated with Man displayed increased cell toxicity, hypodiploid cells, caspase-3 and -9 activity, Bax protein expression, followed with decreased MMP and Bcl-2 protein expression. Inhibition of p38 MAPK signaling pathway markedly reduced apoptosis rate and caspase-3 activity in thymocytes exposed to Man. Application of increasing Cur (1, 3 μM) concentrations resulted with significantly reduced cytotoxicity, apoptosis, caspase-3, -9 activity, Bax protein expression, together with increased MMP and Bcl-2 protein expression in rat thymocytes. These result suggest that certain Cur concentrations may mediate Man-induced rat thymocytes toxicity through mitochondrial survival pathway, which may be useful in preventing possible secondary immunological consequences induced by Man. © 2016 Elsevier Ltd.

Author keywords

CurcuminMancozebMitochondrial survival pathwayThymocytesToxicity

Indexed keywords

EMTREE drug terms:caspase 3caspase 9curcuminmancozebmitogen activated protein kinase p38protein Baxprotein bcl 2curcuminfungicidemancozebmanebzineb
EMTREE medical terms:adultanimal cellapoptosisArticlecell damagecell protectioncell survivalcell viabilityconcentration responsecontrolled studycytotoxicitydisorders of mitochondrial functionsdown regulationdrug effectdrug mechanismenzyme activityhypodiploid cellmalemitochondrial membrane potentialmitochondrionnonhumanprotein expressionprotein functionratsignal transductionthymocyteanimalcell culturedose responsedrug effectsmitochondrionthymocyte
MeSH:AnimalsCells, CulturedCurcuminDose-Response Relationship, DrugFungicides, IndustrialMaleManebMitochondriaRatsThymocytesZineb

Chemicals and CAS Registry Numbers:

caspase 3, 169592-56-7; caspase 9, 180189-96-2; curcumin, 458-37-7; mancozeb, 8018-01-7; protein bcl 2, 219306-68-0; maneb, 12427-38-2; zineb, 12122-67-7;

Curcumin; Fungicides, Industrial; mancozeb; Maneb; Zineb

Manufacturers:

Drug manufacturer:

Sigma Aldrich, United States

  • ISSN: 02786915
  • CODEN: FCTOD
  • Source Type: Journal
  • Original language: English
  • DOI: 10.1016/j.fct.2015.12.029
  • PubMed ID: 26763609
  • Document Type: Article
  • Publisher: Elsevier Ltd

  Pavlovic, V.; Institute of Physiology, Medical Faculty University of Nis, Bulevar Dr. Zorana Djindjica 81, Nis, Serbia;
© Copyright 2017 Elsevier B.V., All rights reserved.

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View details of all 17 citations
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