TY - JOUR
T1 - Cytotoxicity and oxidative damage in kidney cells exposed to the mycotoxins ochratoxin A and citrinin
T2 - Individual and combined effects
AU - Bouslimi, Amel
AU - Ouannes, Zouhour
AU - Golli, Emna
AU - Bouaziz, Chayma
AU - Hassen, Wafa
AU - Bacha, Hassen
N1 - Funding Information:
Received 14 February 2007; accepted 20 May 2007. This research was supported by the “Ministère Tunisien de l’Enseignement Supérieur, de la Recherche Scientifique et de la Technologie” through the “Laboratoire de Recherche sur les Substances Biologiquement Compatibles.” This article is not subject to United States copyright laws. Address correspondence to Pr Hassen Bacha, Laboratory for Research on Biologically Compatible Compounds, Faculty of Dentistry, Rue Avicenne, 5019 Monastir, Tunisia. E-mail: [email protected]
PY - 2008/5
Y1 - 2008/5
N2 - Ochratoxin A (OTA) and citrinin (CTN) are two mycotoxins, quite common contaminants, that can occur jointly in a wide range of food commodities. Both mycotoxins have several toxic effects but both share a significant nephrotoxic potential since OTA and CTN were reported to be responsible for naturally occurring human and animal kidney diseases. Considering the concomitant production of OTA and CTN, it is very likely that humans and animals are always exposed to the mixture rather than to individual compounds. Therefore, the aim of the present study was to investigate, using kidney cell culture (Vero cells), whether cytotoxicity and essentially oxidative cell damage (a key determinant of renal diseases) are enhanced by combination of both mycotoxins as compared to their effect separately. To this end, we have assessed their effects individually or combined on cell proliferation using three different cell viability assays (MTT, Trypan Blue, and Neutral Red). In addition, the role of oxidative stress was investigated by measuring the malondialdehyde (MDA) level and the expression of the heat shock protein Hsp 70. Our results clearly showed that cultured renal cells respond to OTA and CTN exposure by a moderate and weak inhibition of cell proliferation and induction of oxidative stress, respectively. However, when combined, they exert a significant increase in inhibition of cell viability as well as the induction of MDA level and Hsp 70 expression. OTA and CTN combination effects are clearly of synergistic nature. The enhanced induction of oxidative stress observed with OTA and CTN simultaneously could be relevant to explain the molecular basis of the renal diseases induced by these mycotoxins.
AB - Ochratoxin A (OTA) and citrinin (CTN) are two mycotoxins, quite common contaminants, that can occur jointly in a wide range of food commodities. Both mycotoxins have several toxic effects but both share a significant nephrotoxic potential since OTA and CTN were reported to be responsible for naturally occurring human and animal kidney diseases. Considering the concomitant production of OTA and CTN, it is very likely that humans and animals are always exposed to the mixture rather than to individual compounds. Therefore, the aim of the present study was to investigate, using kidney cell culture (Vero cells), whether cytotoxicity and essentially oxidative cell damage (a key determinant of renal diseases) are enhanced by combination of both mycotoxins as compared to their effect separately. To this end, we have assessed their effects individually or combined on cell proliferation using three different cell viability assays (MTT, Trypan Blue, and Neutral Red). In addition, the role of oxidative stress was investigated by measuring the malondialdehyde (MDA) level and the expression of the heat shock protein Hsp 70. Our results clearly showed that cultured renal cells respond to OTA and CTN exposure by a moderate and weak inhibition of cell proliferation and induction of oxidative stress, respectively. However, when combined, they exert a significant increase in inhibition of cell viability as well as the induction of MDA level and Hsp 70 expression. OTA and CTN combination effects are clearly of synergistic nature. The enhanced induction of oxidative stress observed with OTA and CTN simultaneously could be relevant to explain the molecular basis of the renal diseases induced by these mycotoxins.
KW - Citrinin
KW - Combined Effects
KW - Cytotoxicity
KW - Mycotoxins
KW - Ochratoxin A
KW - Oxidative Damage
KW - Renal Toxicity
UR - http://www.scopus.com/inward/record.url?scp=45949099123&partnerID=8YFLogxK
U2 - 10.1080/15376510701556682
DO - 10.1080/15376510701556682
M3 - Article
AN - SCOPUS:45949099123
SN - 1537-6516
VL - 18
SP - 341
EP - 349
JO - Toxicology Mechanisms and Methods
JF - Toxicology Mechanisms and Methods
IS - 4
ER -