scholarly journals Daphnane Diterpenes from Daphne genkwa Activate Nurr1 and Have a Neuroprotective Effect in an Animal Model of Parkinson’s Disease

2016 ◽  
Vol 79 (6) ◽  
pp. 1604-1609 ◽  
Author(s):  
Baek-Soo Han ◽  
Kyoung-Shim Kim ◽  
Yu Jin Kim ◽  
Hoe-Yune Jung ◽  
Young-Mi Kang ◽  
...  
2012 ◽  
Vol 47 (1) ◽  
pp. 117-122 ◽  
Author(s):  
Hong-Hua Yuan ◽  
Ren-Jin Chen ◽  
Yu-Hua Zhu ◽  
Chang-Ling Peng ◽  
Xiao-Rong Zhu

2015 ◽  
Vol 51 (1) ◽  
pp. 111-115 ◽  
Author(s):  
Débora Dalla Vecchia ◽  
Marissa Giovanna Schamne ◽  
Marcelo Machado Ferro ◽  
Ana Flávia Chaves dos Santos ◽  
Camila Lupepsa Latyki ◽  
...  

Parkinson's disease (PD) is an age-related neurodegenerative disorder characterized by the slow and progressive death of dopaminergic neurons in the (substantia nigra pars compact). Hypericum perforatum (H. perforatum) is a plant widely used as an antidepressant, that also presents antioxidant and anti-inflammatory properties. We evaluated the effects of H. perforatum on the turning behavior of rats submitted to a unilateral administration of 6-hydroxydopamine (6-OHDA) into the medial forebrain bundle as an animal model of PD. The animals were treated with H. perforatum (100, 200, or 400 mg/kg, v.o.) for 35 consecutive days (from the 28th day before surgery to the 7th day after). The turning behavior was evaluated at 7, 14 and 21 days after the surgery, and the turnings were counted as contralateral or ipsilateral to the lesion side. All tested doses significantly reduced the number of contralateral turns in all days of evaluation, suggesting a neuroprotective effect. However, they were not able to prevent the 6-OHDA-induced decrease of tyrosine hydroxylase expression in the lesioned striatum. We propose that H. perforatum may counteract the overexpression of dopamine receptors on the lesioned striatum as a possible mechanism for this effect. The present findings provide new evidence that H. perforatum may represent a promising therapeutic tool for PD.


2015 ◽  
Vol 29 (3) ◽  
pp. 351-363 ◽  
Author(s):  
Agnieszka Wąsik ◽  
Irena Romańska ◽  
Jerzy Michaluk ◽  
Agnieszka Zelek-Molik ◽  
Irena Nalepa ◽  
...  

2016 ◽  
Vol 30 (2) ◽  
pp. 283-283
Author(s):  
Agnieszka Wasik ◽  
Irena Romańska ◽  
Jerzy Michaluk ◽  
Agnieszka Zelek-Molik ◽  
Irena Nalepa ◽  
...  

2015 ◽  
Vol 2015 ◽  
pp. 1-7 ◽  
Author(s):  
Souravh Bais ◽  
N. S. Gill ◽  
Nitan Kumar

We evaluated anti-Parkinson’s activity of methanolic extract of Juniperus communis (MEJC) leaves in chlorpromazine (CPZ) induced experimental animal model. In this study effects of Juniperus communis (100 and 200 mg/kg, i.p.) were studied using various behavior parameters like catalepsy (bar test), muscle rigidity (rotarod test), and locomotor activity (actophotometer) and its effect on neurochemical parameters (TBARS, GSH, nitrite, and total protein) in rats. The experiment was designed, by giving chlorpromazine (3 mg/kg, i.p.) for 21 days to induce Parkinson’s disease-like symptoms. Chlorpromazine significantly induced motor dysfunctions (catalepsy, muscle rigidity, and hypolocomotion) in a period of 21 days. The MEJC significantly (P<0.001) reduced catalepsy and muscle rigidity and significantly (P<0.001) increased locomotor activity in rats. The maximum reduction was observed on the 21st day at a dose of 200 mg/kg (i.p.). The MEJC extract also showed an increase in the level of reduced gutathione (GSH) (P<0.001) and total protein (P<0.001) and decreased the elevated levels of TBARS (P<0.001) and nitrite (P<0.001) preferably at a higher dose (200 mg/kg) as compared to chlorpromazine group. Thus the present study showed the neuroprotective effect of MEJC against CPZ induced Parkinson’s disease-like symptoms or anti-Parkinson’s activity.


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