Pituitary adenylate cyclase activating polypeptide protects dopaminergic neurons and improves behavioral deficits in a rat model of Parkinson's disease

被引:93
作者
Reglödi, D [1 ]
Lubics, A [1 ]
Tamás, A [1 ]
Szalontay, L [1 ]
Lengvári, I [1 ]
机构
[1] Univ Pecs, Hungarian Acad Sci, Neurohumoral Regulat Res Grp, Fac Med,Dept Anat, H-7624 Pecs, Hungary
基金
匈牙利科学研究基金会;
关键词
PACAP; neuroprotection; Parkinson's disease; tyrosine-hydroxylase; substantia nigra;
D O I
10.1016/j.bbr.2003.09.007
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
Pituitary adenylate cyclase activating polypeptide (PACAP) is a pleiotropic neuropeptide, exerting different actions in the central and peripheral nervous systems. Among others, it has neurotrophic and neuroprotective effects. In the present study, we investigated the effects of PACAP in a rat model of Parkinson's disease. Rats were given unilateral injections of 6-hydroxydopamine (6-OHDA) into the substantia nigra. PACAP-treated animals received 0.1 mug PACAP as a pretreatment. Control animals without PACAP treatment displayed severe hypokinesia at 1 and 10 days postlesion when compared to animals receiving saline only. In only I day postlesion, by contrast, PACAP-treated rats showed no hypokinesia. Asymmetrical signs, such as turning, rearing and biased thigmotaxic scanning were observed in all lesioned animals 1 day postlesion. PACAP-treated animals, however, showed better recovery as they ceased to display asymmetrical signs 10 days later and showed markedly less apomorphine-induced rotations. Tyrosine-hydroxylase immunohistochemistry revealed that control animals had more than 95% loss of the dopaminergic cells in the ipsilateral substantia nigra, while PACAP-treated animals had only approximately 50% loss of dopaminergic cells. In summary, the present results show the neuroprotective effect of PACAP in 6-OHDA-induced lesion of substantia nigra, with less severe acute neurological symptoms and a more rapid amelioration of behavioral deficits. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:303 / 312
页数:10
相关论文
共 70 条
[1]   Perspectives on pituitary adenylate cyclase activating polypeptide (PACAP) in the neuroendocrine, endocrine, and nervous systems [J].
Arimura, A .
JAPANESE JOURNAL OF PHYSIOLOGY, 1998, 48 (05) :301-331
[2]   VASOACTIVE-INTESTINAL-PEPTIDE PREVENTS LUNG INJURY DUE TO XANTHINE XANTHINE-OXIDASE [J].
BERISHA, H ;
FODA, H ;
SAKAKIBARA, H ;
TROTZ, M ;
PAKBAZ, H ;
SAID, SI .
AMERICAN JOURNAL OF PHYSIOLOGY, 1990, 259 (02) :L151-L155
[3]   1-trichloromethyl-1,2,3,4-tetrahydro-β-carboline (TaClo) and related derivatives:: Chemistry and biochemical effects on catecholamine biosynthesis [J].
Bringmann, G ;
Feineis, D ;
God, R ;
Peters, K ;
Peters, EM ;
Scholz, J ;
Riederer, F ;
Moser, A .
BIOORGANIC & MEDICINAL CHEMISTRY, 2002, 10 (07) :2207-2214
[4]   NAIP protects the nigrostriatal dopamine pathway in an intrastriatal 6-OHDA rat model of Parkinson's disease [J].
Crocker, SJ ;
Wigle, N ;
Liston, P ;
Thompson, CS ;
Lee, CJ ;
Xu, DG ;
Roy, S ;
Nicholson, DW ;
Park, DS ;
MacKenzie, A ;
Korneluk, RG ;
Robertson, GS .
EUROPEAN JOURNAL OF NEUROSCIENCE, 2001, 14 (02) :391-400
[5]  
Czlonkowska Anna, 2002, Med Sci Monit, V8, pRA165
[6]  
Delgado M, 1999, J IMMUNOL, V162, P2358
[7]   Neuroprotective effect of vasoactive intestinal peptide (VIP) in a mouse model of Parkinson's disease by blocking microglial activation [J].
Delgado, M ;
Ganea, D .
FASEB JOURNAL, 2003, 17 (03) :944-+
[8]   Vasoactive intestinal peptide and pituitary adenylate cyclase-activating polypeptide inhibit the production of inflammatory mediators by activated microglia [J].
Delgado, M ;
Leceta, J ;
Ganea, D .
JOURNAL OF LEUKOCYTE BIOLOGY, 2003, 73 (01) :155-164
[9]   Modeling Parkinsn's disease in rats: An evaluation of 6-OHDA lesions of the nigrostriatal pathway [J].
Deumens, R ;
Blokland, A ;
Prickaerts, J .
EXPERIMENTAL NEUROLOGY, 2002, 175 (02) :303-317
[10]   Caspase-3-like proteases and 6-hydroxydopamine induced neuronal cell death [J].
Dodel, RC ;
Du, YS ;
Bales, KR ;
Ling, ZD ;
Carvey, PM ;
Paul, SM .
MOLECULAR BRAIN RESEARCH, 1999, 64 (01) :141-148