Neuroprotective activity of tetramethylpyrazine against 3-nitropropionic acid induced Huntington's disease-like symptoms in rats

被引:51
作者
Danduga, Ravi Chandra Sekhara Reddy [1 ]
Dondapati, Subba Reddy [2 ]
Kola, Phani Kumar [1 ]
Grace, Lilly [1 ]
Tadigiri, Rahil Vandana Bisky [1 ]
Kanakaraju, Vijaya Kishore [3 ]
机构
[1] Acharya Nagarjuna Univ, Univ Coll Pharmaceut Sci, Dept Pharmacol, Guntur 522510, India
[2] Nirmala Coll Pharm, Dept Pharmacol, Atmakur, Andhra Prades, India
[3] Acharya Nagarjuna Univ, Univ Coll Pharmaceut Sci, Dept Pharmaceut Chem, Guntur, India
关键词
Huntington's disease; 3-nitropropionic acid; Tetramethylpyrazine; Oxidative stress; Neurochemicals; Histopathology; FOCAL CEREBRAL-ISCHEMIA; ANTI-APOPTOTIC ACTIONS; OXIDATIVE STRESS; MITOCHONDRIAL DYSFUNCTION; STRIATAL DEGENERATION; 3-NP-INDUCED NEUROTOXICITY; PARKINSONS-DISEASE; FREE-RADICALS; BRAIN-INJURY; MODEL;
D O I
10.1016/j.biopha.2018.06.079
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Huntington's disease (HD) is an autosomal neurodegenerative disease characterized by chorea, dystonia, motor ataxia, cognitive decline and psychiatric disorders with gradual loss of nerve cells and has no existing cure for the disease. In the present study, a mitochondrial toxin, 3-nitropropionic acid (3-NP) is used to induce HD like symptoms in rats. Tetramethylpyrazine is one of the active ingredients of Chuan Xiong which was reported to have neurotrophic and neuroprotective activities. The present study was designed to evaluate the role of TMP on 3-NP induced behavioral, biochemical, neurochemical, and histological alterations in the different regions of the brain. Animals were pretreated with normal saline/TMP for 7 days. From 8th day, the treatment groups were coadministered with 3-NP (10 mg/kg, i.p) and continued to the 21st day of the treatment protocol. At the end of the study, we found that the TMP improved all the behavioral performances of 3-NP induced neurotoxic rats, significantly. Further, oxidative stress parameters (lipid peroxidation, reduced glutathione, catalase, and superoxide dismutase), succinate dehydrogenase enzyme, and neurochemical (GABA and glutamate) estimations were done in the brain homogenate. In our study, the treatment with TMP ameliorated the 3-NP induced alterations, in the biochemical and neurochemical parameter in the brain homogenate, dose-dependently. The protective role of TMP further confirmed by measuring the lesion area with the 2,3,5-triphenyltetrazolium chloride staining of the brain slices and histopathological alteration in the hippocampus (CA1 and CA3) and striatal regions of the brain. Hence, the present findings suggest that the protective role of TMP against 3-NP induced behavioral, biochemical, neurochemical, and histological alterations in rats.
引用
收藏
页码:1254 / 1268
页数:15
相关论文
共 93 条
[1]   Protective effect of minocycline, a semi-synthetic second-generation tetracycline against 3-nitropropionic acid (3-NP)-induced neurotoxicity [J].
Ahuja, Manuj ;
Bishnoi, Mahendra ;
Chopra, Kanwaljit .
TOXICOLOGY, 2008, 244 (2-3) :111-122
[2]   Effect of thioperamide on modified forced swimming test-induced oxidative stress in mice [J].
Akhtar, M ;
Pillai, KK ;
Vohora, D .
BASIC & CLINICAL PHARMACOLOGY & TOXICOLOGY, 2005, 97 (04) :218-221
[3]   Effect of thioperamide on oxidative stress markers in middle cerebral artery occlusion model of focal cerebral ischemia in rats [J].
Akhtar, M. ;
Pillai, K. K. ;
Vohora, D. .
HUMAN & EXPERIMENTAL TOXICOLOGY, 2008, 27 (10) :761-767
[4]  
BEAL MF, 1993, J NEUROSCI, V13, P4181
[5]   EVALUATION OF 2, 3, 5-TRIPHENYLTETRAZOLIUM CHLORIDE AS A STAIN FOR DETECTION AND QUANTIFICATION OF EXPERIMENTAL CEREBRAL INFARCTION IN RATS [J].
BEDERSON, JB ;
PITTS, LH ;
GERMANO, SM ;
NISHIMURA, MC ;
DAVIS, RL ;
BARTKOWSKI, HM .
STROKE, 1986, 17 (06) :1304-1308
[6]   INFLUENCE OF AGING AND NEURODEGENERATION ON DENDRITIC SPINE MORPHOLOGY [J].
Bloss, Erik B. ;
Morrison, John H. ;
Hof, Patrick R. ;
Dickstein, Dara L. .
TRANSLATIONAL NEUROSCIENCE, 2011, 2 (01) :49-60
[7]   SYSTEMIC 3-NITROPROPIONIC ACID - BEHAVIORAL DEFICITS AND STRIATAL DAMAGE IN ADULT-RATS [J].
BORLONGAN, CV ;
KOUTOUZIS, TK ;
RANDALL, TS ;
FREEMAN, TB ;
CAHILL, DW ;
SANBERG, PR .
BRAIN RESEARCH BULLETIN, 1995, 36 (06) :549-556
[8]  
Bouvier E, 2017, MOL PSYCHIATR, V22, P1701, DOI 10.1038/mp.2016.144
[9]   3-Nitropropionic acid: a mitochondrial toxin to uncover physiopathological mechanisms underlying striatal degeneration in Huntington's disease [J].
Brouillet, E ;
Jacquard, C ;
Bizat, N ;
Blum, D .
JOURNAL OF NEUROCHEMISTRY, 2005, 95 (06) :1521-1540
[10]   PROFILIN-2 INCREASED EXPRESSION AND ITS ALTERED INTERACTION WITH β-ACTIN IN THE STRIATUM OF 3-NITROPROPIONIC ACID-INDUCED HUNTINGTON'S DISEASE IN RATS [J].
Chakraborty, J. ;
Pandey, M. ;
Navneet, A. K. ;
Appukuttan, T. A. ;
Varghese, M. ;
Sreetama, S. C. ;
Rajamma, U. ;
Mohanakumar, K. P. .
NEUROSCIENCE, 2014, 281 :216-228