Protective effect of Calligonum comosum on haloperidol-induced oxidative stress in rat

被引:33
作者
Abdel-Sattar, Essam A. [1 ]
Mouneir, Samar M. [2 ,3 ]
Asaad, Gihan F. [4 ]
Abdallah, Hossam M. [1 ,5 ]
机构
[1] Cairo Univ, Fac Pharm, Dept Pharmacognosy, Cairo 11562, Egypt
[2] Cairo Univ, Dept Pharmacol, Fac Vet Med, Cairo 11562, Egypt
[3] Taif Univ, Fac Clin Pharm, Dept Pharmacol & Toxicol, At Taif, Saudi Arabia
[4] Natl Res Ctr, Dept Pharmacol, Giza, Egypt
[5] King Abdulaziz Univ, Fac Pharm, Dept Nat Prod & Alternat Med, Jeddah 21413, Saudi Arabia
关键词
Calligonum comosum; antioxidant; neurotoxicity; hepatotoxicity; haloperidol; neurotanmitters; dopaminergic effect; INDUCED CATALEPSY; DOPAMINE; DRUGS; LIVER;
D O I
10.1177/0748233712452601
中图分类号
R1 [预防医学、卫生学];
学科分类号
100235 [预防医学];
摘要
The aqueous and methanolic extracts of Calligonum comosum were investigated for their antioxidant and dopaminergic effects on haloperidol (HL)-induced neuro- and hepatotoxicities in male albino rat model. The total phenolics, flavonoid content and free radical-scavenging activity of the extracts were determined. The results showed that the antioxidant activity of the methanolic extract was higher than the aqueous one. HL significantly reduced GSH and increased MDA in brain and liver tissues. These values were nearly normalized, in the examined tissues, on concomitant administration of C. comosum methanolic extract with HL. Superoxide dismutase activity in the examined tissues was significantly decreased by HL administration that was normalized by the coadministration of the methanolic extract and, to a less extent, the water extract. Determination of the brain neurotransmitter contents revealed a marked decrease in norepinephrine, dopamine and serotonin, which were restored to near control values by concomitant administration of both C. comosum extracts with HL. The results of this study showed that C. comosum methanolic and aqueous extracts ameliorated HL-induced neuro- and hepatotoxicities in rats.
引用
收藏
页码:147 / 153
页数:7
相关论文
共 29 条
[1]
Arjuman A, 2007, INDIAN J PHARMACOL, V39, P151
[2]
Badria FA, 2007, Z NATURFORSCH C, V62, P656
[3]
RELATIVE CYTOTOXICITY OF PSYCHOTROPIC-DRUGS IN CULTURED RAT HEPATOCYTES [J].
BOELSTERLI, UA ;
BOUIS, P ;
DONATSCH, P .
CELL BIOLOGY AND TOXICOLOGY, 1987, 3 (03) :231-250
[4]
Bogdan M, 2011, ROM J MORPHOL EMBRYO, V52, P465
[5]
Antioxidant principles from Bauhinia tarapotensis [J].
Braca, A ;
De Tommasi, N ;
Di Bari, L ;
Pizza, C ;
Politi, M ;
Morelli, I .
JOURNAL OF NATURAL PRODUCTS, 2001, 64 (07) :892-895
[6]
Ionization-reactivity relationships for cysteine thiols in polypeptides [J].
Bulaj, G ;
Kortemme, T ;
Goldenberg, DP .
BIOCHEMISTRY, 1998, 37 (25) :8965-8972
[7]
EL-HAWARY Z M, 1990, Archives of Pharmacal Research (Seoul), V13, P113, DOI 10.1007/BF02857846
[8]
Elberry AA., 2015, Int J Diabetes Mellitus, V3, P37, DOI [10.1016/j.ijdm.2011.01.004, DOI 10.1016/J.IJDM.2011.01.004]
[9]
TISSUE SULFHYDRYL GROUPS [J].
ELLMAN, GL .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1959, 82 (01) :70-77
[10]
FARDE L, 1992, ARCH GEN PSYCHIAT, V49, P538