3,4-Methylenedioxymethamphetamine (MDMA), but not morphine, alters APP processing in the rat brain

被引:4
|
作者
Kalman, Janos
Bjelik, Annamaria
Hugyecz, Marietta
Timar, Julia
Gyarmati, Zsuzsanna
Zana, Marianna
Furst, Zsuzsanna
Janka, Zoltan
Rakonczay, Zoltan
Horvath, Zoltan
Pakaski, Magdona
机构
[1] Univ Szeged, Dept Psychiat, Fac Med, Albert Schent Gyorgyi Ctr Med & Pharmaceut Sci, H-6725 Szeged, Hungary
[2] Univ Szeged, Alzheimers Dis Res Ctr, Fac Med, Albert Schent Gyorgyi Ctr Med & Pharmaceut Sci, H-6725 Szeged, Hungary
[3] Semmelweis Univ, Dept Pharmacol, H-1085 Budapest, Hungary
[4] Semmelweis Univ, Dept Pharmacotherapy, H-1085 Budapest, Hungary
[5] Semmelweis Univ, Hungarian Acad Sci, Neuropsychopharmacol Grp, H-1085 Budapest, Hungary
[6] Univ Szeged, Dept Oral Biol, Fac Med, Albert Schent Gyorgyi Ctr Med & Pharmaceut Sci, H-6725 Szeged, Hungary
来源
关键词
Alzheimer's disease; amyloid; amyloid precursor protein; immunoblotting; MDMA; morphine; mRNA; beta-secretase;
D O I
10.1017/S146114570600650X
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The abuse of drugs such as opioids and 3,4-methylenedioxymethamphetamine (MDMA or 'ecstasy') can have detrimental effects on the cognitive functions, but the exact molecular mechanism whereby these drugs promote neuroclegeneration remains to be elucidated. The major purpose of the present pilot study was to determine whether the chronic in-vivo administration of morphine (10 mg/kg) or MDMA (I mg/kg) to rats can alter the expression and processing of amyloid precursor protein (APP), the central molecule in the proposed pathomechanism of Alzheimer's disease. MDMA treatment significantly decreased the production of APP in the cytosolic fraction of the brain cortex. A concomitant 25 % increase was found both in the beta-secretase (BACE) and APP mRNA levels (108 %). In contrast, in the applied single dosage chronic morphine treatment did not influence either the APP and BACE protein levels or the APP mRNA production. These results indicate that the chronic use of 'ecstasy', but not morphine, may be harmful via a novel mode of action, i.e. by altering the APP expression and processing in the brain.
引用
收藏
页码:183 / 190
页数:8
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