Hepatoprotective effects of the n-butanol extract from Perralderia coronopifolia Coss. against PCP-induced toxicity in Wistar albino rats.
1-Butanol
/ chemistry
Alanine Transaminase
/ blood
Animals
Antioxidants
/ metabolism
Aspartate Aminotransferases
/ blood
Asteraceae
/ chemistry
Chemical and Drug Induced Liver Injury
/ metabolism
Female
Glutathione
/ metabolism
Glutathione Peroxidase
/ metabolism
Lipid Peroxidation
/ drug effects
Liver
/ drug effects
Pentachlorophenol
/ toxicity
Plant Extracts
/ chemistry
Protective Agents
/ chemistry
Rats, Wistar
Antioxidant enzymes
Glutathione
Hepatotoxicity
Lipid peroxidation level
Pentachlorphenol
Perralderia coronopifolia
Journal
Environmental science and pollution research international
ISSN: 1614-7499
Titre abrégé: Environ Sci Pollut Res Int
Pays: Germany
ID NLM: 9441769
Informations de publication
Date de publication:
Oct 2019
Oct 2019
Historique:
received:
11
11
2018
accepted:
16
08
2019
pubmed:
30
8
2019
medline:
8
1
2020
entrez:
30
8
2019
Statut:
ppublish
Résumé
In the present study, in vivo antioxidant properties of the n-butanol extract obtained from aerial parts of Perralderia coronopifolia were investigated in term of its hepatoprotective effect of female Wistar albino rats (n, 36; average age, 48 ± 5 days; weighing 150 ± 18 g) against PCP (pentachlorphenol)-induced toxicity. PCP (20 mg/kg b.w.) and plant extract (50 mg/kg b.w.) were administered daily by gavages for 2 weeks. Vitamin E (100 mg/kg b.w.) was given intraperitoneally as a positive control. Lipid peroxidation (LPO) levels, reduced glutathione (GSH) levels, and glutathione peroxidase (GPx) activities were evaluated in liver homogenates. While, aspartate aminotransferase (AST), alanine aminotransferase (ALT), cholesterol, and triglyceride parameters were analyzed in serums. The liver fragments were observed using light microscopy. Experimental results exhibited that PCP-treated group has a significant increase in the liver lipid peroxidation (LPO) levels of animals while decreased in plant extract-treated group. In addition, PCP caused significant decreases in glutathione peroxidase (GPx) activities and reduced glutathione (GSH) levels. Moreover, PCP induced hepatotoxicity by increasing serum transaminase enzymes, cholesterol, and triglyceride levels. While, these levels were restored to control value in animals treated with plant extract. The regularized levels of LPO, GSH, cholesterol, triglyceride, transaminase enzymes, and GPx activities revealed the antioxidant properties of the extract plant as well as of the vitamin E. The histological study showed the hepatoprotective effect of our extracts against PCP-induced acute intoxication, protecting the hepatic architecture and decreasing the functional and structural alterations of the liver. The plant extract had high antioxidant potential and completely prevented the toxic effect of PCP on the above of liver and serum parameters.
Identifiants
pubmed: 31463753
doi: 10.1007/s11356-019-06231-6
pii: 10.1007/s11356-019-06231-6
doi:
Substances chimiques
Antioxidants
0
Plant Extracts
0
Protective Agents
0
1-Butanol
8PJ61P6TS3
Pentachlorophenol
D9BSU0SE4T
Glutathione Peroxidase
EC 1.11.1.9
Aspartate Aminotransferases
EC 2.6.1.1
Alanine Transaminase
EC 2.6.1.2
Glutathione
GAN16C9B8O
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
31215-31224Références
Cardiovasc Hematol Disord Drug Targets. 2017 Jul 4;17(1):18-23
pubmed: 28294073
Comp Biochem Physiol C Toxicol Pharmacol. 2011 Mar;153(2):175-90
pubmed: 20959147
Chem Res Toxicol. 2009 Jun;22(6):969-77
pubmed: 19408893
Methods Enzymol. 1984;105:114-21
pubmed: 6727659
Zhongguo Zhong Yao Za Zhi. 2015 Feb;40(4):588-93
pubmed: 26137674
Chemosphere. 2017 Jun;177:44-50
pubmed: 28284116
Environ Toxicol Chem. 2014 Jan;33(1):170-6
pubmed: 24123209
J Ethnopharmacol. 2013 Jul 9;148(2):664-70
pubmed: 23707208
Food Chem Toxicol. 1995 Oct;33(10):877-82
pubmed: 7590532
Chin Med J (Engl). 1996 May;109(5):366-71
pubmed: 9208493
Environ Sci Technol. 2015 Oct 6;49(19):11894-902
pubmed: 26378342
J Biol Chem. 1951 Nov;193(1):265-75
pubmed: 14907713
Arch Biochem Biophys. 1959 May;82(1):70-7
pubmed: 13650640
Toxicol Lett. 2001 Jun 20;122(2):157-69
pubmed: 11439222
Comp Biochem Physiol C Comp Pharmacol Toxicol. 1992 Feb;101(2):353-63
pubmed: 1354112
Asian Pac J Trop Biomed. 2012 Aug;2(8):645-50
pubmed: 23569987
Gen Pharmacol. 1995 May;26(3):453-62
pubmed: 7789717
Free Radic Biol Med. 1998 Jun;24(9):1477-84
pubmed: 9641266
J Hazard Mater. 2015;283:897-904
pubmed: 25464334
Toxicology. 2005 May 15;210(1):37-44
pubmed: 15804456
Int J Toxicol. 2002 Jul-Aug;21(4):301-18
pubmed: 12171631
Chem Biol Interact. 2000 Nov 1;128(3):173-88
pubmed: 11064002
Chem Biol Interact. 1990;74(3):305-14
pubmed: 2161290
Molecules. 2019 Jan 02;24(1):
pubmed: 30609767
J Med Food. 2017 Dec;20(12):1193-1200
pubmed: 29131698
Anal Biochem. 1978 May;86(1):271-8
pubmed: 655387
J Environ Sci Health B. 2003 May;38(3):349-63
pubmed: 12716052
Toxicology. 2003 Jul 15;189(1-2):113-27
pubmed: 12821287
Comp Biochem Physiol C Toxicol Pharmacol. 2009 Aug;150(2):179-85
pubmed: 19410655
Cell Biol Toxicol. 2004 May;20(3):183-96
pubmed: 15250542
Chemosphere. 2019 Apr;220:216-226
pubmed: 30583213