The Effect of Crude Extract and Fractions of Teucrium polium L. on the Brain, Liver, and Kidney of Male Rats

被引:0
作者
Nematollahi-Mahani, Seyed Noureddin [1 ,2 ,3 ]
Ganjalikhan-Hakemi, Sepideh [1 ]
Abdi, Zahra [4 ]
机构
[1] Kerman Univ Med Sci, Afzalipour Sch Med, Dept Anat, Kerman, Iran
[2] Kerman Univ Med Sci, Neurosci Res Ctr, Inst Neuropharmacol, Kerman, Iran
[3] Afzal Res Inst NGO, Kerman, Iran
[4] Zanjan Univ Med Sci, Sch Med, Dept Anat Sci, Zanjan, Iran
关键词
Teucrium polium; Toxicity; Brain; Kidney; Liver; HUMAN-CELLS; HEPATITIS; HEPATOTOXICITY; EXPRESSION; GERMANDER; GROWTH; PLANTS; TUMORS;
D O I
10.5812/jjnpp.112160
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background: Teucrium polium (TP) is a medicinal plant with a long history of consumption as a folk remedy for curing many diseases, including diabetes, common cold, obesity, anxiety, etc. Objectives: The present study aimed at investigating the effects of TP crude extracts (TPCE), as well as its diethyl ether (DE) and petroleum ether (PE) fractions, on the brain, kidney, and liver tissue of male rats in the subchronic phase. Methods: In the study, 45 adult male Wistar rats were randomly assigned to five groups as the PBS (receiving phosphate buffer saline), vehicle (receiving dimethyl sulfoxide), as well as CE, PE, and DE receiving 3 mg/kg (100 mu L) TPCE, PE, and DE, respectively, for sixweeks. Histopathological examinations by hematoxylin and eosin staining investigated morphological changes in all specimens. Also, the brain samples were stained by the immunohistochemistry(IHC) technique with Ki-67, CD31, p53, Nestin, and GFAP markers. Results: The findings showed that the prolonged consumption of TP caused the formation of histological lesions as apoptosis, degeneration, cytoplasmic vacuolization of neurons, and foamy cells in the brain. The liver, displayed cytoplasmic vacuolization, apoptosis, degeneration, and dilated sinusoids. Moreover, TP led to atrophy, vacuolization, and necrosis in renal cells. IHC studies evidenced an increase in the expression of P53, whereas the expression of Ki67 and CD31 decreased. It should be noted that TP crude extract and fractions were toxic; however, the PE fraction was more cytotoxic than others. Conclusions: The study findings indicated that long-term administration of a sublethal dose of TP impairs cellular integrity in vital orangs, including the liver, brain, and kidney, through triggering the cell death mechanisms.
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页数:10
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共 39 条
[1]   Effects of Two Types of Human Cells on Outgrowth of Human Glioma in Rats [J].
Abdi, Zahra ;
Eskandary, Hossien ;
Nematollahi-Mahani, Seyed Noureddin .
TURKISH NEUROSURGERY, 2018, 28 (01) :19-28
[2]  
Akerele O, 1993, World Health Forum, V14, P390
[3]  
Al-Ashban R. M., 2005, Journal of Herbs, Spices & Medicinal Plants, V11, P27, DOI 10.1300/J044v11n04_04
[4]  
AUTORE G, 1984, PHARMACOL RES COMMUN, V16, P21
[5]   Protective effects of four Iranian medicinal plants against free radical-mediated protein oxidation [J].
Bahramikia, Seifollah ;
Ardestani, Amin ;
Yazdanparast, Razieh .
FOOD CHEMISTRY, 2009, 115 (01) :37-42
[6]   Some aspects of toxic contaminants in herbal medicines [J].
Chan, K .
CHEMOSPHERE, 2003, 52 (09) :1361-1371
[7]   Herbal bioactivation, molecular targets and the toxicity relevance [J].
Chen, Xiao-Wu ;
Serag, Erini S. ;
Sneed, Kevin B. ;
Zhou, Shu-Feng .
CHEMICO-BIOLOGICAL INTERACTIONS, 2011, 192 (03) :161-176
[8]   Structure elucidation and hepatotoxicity evaluation against HepG2 human cells of neo-clerodane diterpenes from Teucrium polium L. [J].
Fiorentino, Antonio ;
D'Abrosca, Brigida ;
Pacifico, Severina ;
Scognamiglio, Monica ;
D'Angelo, Grazia ;
Gallicchio, Marialuisa ;
Chambery, Angela ;
Monaco, Pietro .
PHYTOCHEMISTRY, 2011, 72 (16) :2037-2044
[9]   Vascular endothelial growth factor receptor-3 (VEGFR-3): A marker of vascular tumors with presumed lymphatic differentiation, including Kaposi's sarcoma, kaposiform and Dabska-type hemangioendotheliomas, and a subset of angiosarcomas [J].
Folpe, AL ;
Veikkola, T ;
Valtola, R ;
Weiss, SW .
MODERN PATHOLOGY, 2000, 13 (02) :180-185
[10]  
Forouzandeh H, 2013, IRAN J PHARM RES, V12, P123