A novel thiol antioxidant that crosses the blood brain barrier protects dopaminergic neurons in experimental models of Parkinson's disease

被引:56
作者
Bahat-Stroomza, M
Gilgun-Sherki, Y
Offen, D
Panet, H
Saada, A
Krool-Galron, N
Barzilai, A
Atlas, D
Melamed, E
机构
[1] Tel Aviv Univ, Sackler Sch Med, Felsenstein Med Res Ctr, Neurosci Lab, IL-49100 Petah Tiqwa, Israel
[2] Tel Aviv Univ, Sackler Sch Med, Rabin Med Ctr, Dept Neurol, IL-49100 Petah Tiqwa, Israel
[3] Hebrew Univ Jerusalem, Inst Life Sci, Dept Biol Chem, IL-91904 Jerusalem, Israel
[4] Shaare Zedek Med Ctr, Metab Dis Unit, Jerusalem, Israel
[5] Tel Aviv Univ, George S Wise Fac Life Sci, Dept Neurobiochem, IL-69978 Tel Aviv, Israel
关键词
AD4; antioxidants; MPTP; 6-OHDA; oxidative stress; Parkinson's disease; rotenone;
D O I
10.1111/j.1460-9568.2005.03889.x
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
It is believed that oxidative stress (OS) plays an important role in the loss of dopaminergic nigrostriatal neurons in Parkinson's disease (PD) and that treatment with antioxidants might be neuroprotective. However, most currently available antioxidants cannot readily penetrate the blood brain barrier after systemic administration. We now report that AD4, the novel low molecular weight thiol antioxidant and the N-acytel cysteine (NAC) related compound, is capable of penetrating the brain and protects neurons in general and especially dopaminergic cells against various OS-generating neurotoxins in tissue cultures. Moreover, we found that treatment with AD4 markedly decreased the damage of dopaminergic neurons in three experimental models of PD. AD4 suppressed amphetamine-induced rotational behaviour in rats with unilateral 6-OHDA-induced nigral lesion. It attenuated the reduction in striatal dopamine levels in mice treated with 1-methyl-4-phenyl-1,2,3,6,-tetrahydropyridine (MPTP). It also reduced the dopaminergic neuronal loss following chronic intrajugular administration of rotenone in rats. Our findings suggest that AD4 is a novel potential new neuroprotective drug that might be effective at slowing down nigral neuronal degeneration and illness progression in patients with PD.
引用
收藏
页码:637 / 646
页数:10
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