Anticonvulsant evaluation of aminoalkanol derivatives of 2-and 4-methylxanthone

被引:19
作者
Szkaradek, Natalia [1 ]
Gunia, Agnieszka [1 ]
Waszkielewicz, Anna M. [1 ]
Antkiewicz-Michaluk, Lucyna [2 ]
Cegla, Marek [3 ]
Szneler, Edward [4 ]
Marona, Henryk [1 ]
机构
[1] Jagiellonian Univ, Dept Bioorgan Chem, Chair Organ Chem, Fac Pharm,Med Coll, Krakow, Poland
[2] Polish Acad Sci, Inst Pharmacol, Krakow, Poland
[3] Jagiellonian Univ, Chair Organ Chem, Fac Pharm, Coll Med, Krakow, Poland
[4] Jagiellonian Univ, Fac Chem, PL-30060 Krakow, Poland
关键词
Anticonvulsant; MES; Neurotoxicity; Xanthone; Synthesis; XANTHONE DERIVATIVES; ANTIEPILEPTIC DRUGS; ACIDS;
D O I
10.1016/j.bmc.2012.12.051
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A series of 17 new aminoalkanol derivatives of 6-methoxy- or 7-chloro-2-methylxanthone as well as 6-methoxy-4-methylxanthone was synthesized and evaluated for anticonvulsant activity. All compounds were verified in mice after intraperitoneal (ip) administration in maximal electroshock (MES) and subcutaneous pentetrazole (scMet) induced seizures as well as neurotoxicity assessment. Eleven of the tested substances showed protection against electrically evoked seizures in the majority of the tested mice at the dose of 100 mg/kg. Additionally, one was effective at the dose of 30 mg/kg. Five substances were active at the dose of 300 mg/kg or at the dose of 100 mg/kg in the minority of the tested mice. The most promising compound revealed ED50 value of 47.57 mg/kg in MES (mice, ip, 1 h after administration) and at the same time its TD50 was evaluated as above 400 mg/kg. Those values gave PI (calculated as TD50/ED50) of more than 8.41. Three other synthesized xanthone derivatives also proved to act as anticonvulsants and showed ED50 values in MES test (mice, ip) ranged 80-110 mg/kg. Results were quite encouraging and suggested that in the group of xanthone derivatives new potential anticonvulsants might be found. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1190 / 1198
页数:9
相关论文
共 28 条
[1]   Pharmacological characterization of the 6 Hz psychomotor seizure model of partial epilepsy [J].
Barton, ME ;
Klein, BD ;
Wolf, HH ;
White, HS .
EPILEPSY RESEARCH, 2001, 47 (03) :217-227
[2]  
BROWN WC, 1953, J PHARMACOL EXP THER, V107, P273
[3]  
DARE P, 1968, ARZNEI-FORSCHUNG, V18, P718
[4]  
GAION RM, 1982, ARZNEIMITTELFORSCH, V32-1, P499
[5]  
Jastrzebska-Wiesek M, 2008, ACTA POL PHARM, V65, P591
[6]   Allopregnanolone analogs that positively modulate GABAA receptors protect against partial seizures induced by 6-Hz electrical stimulation in mice [J].
Kaminski, RM ;
Livingood, MR ;
Rogawski, MA .
EPILEPSIA, 2004, 45 (07) :864-867
[7]   Animal models used in the screening of antiepileptic drugs [J].
Kupferberg, H .
EPILEPSIA, 2001, 42 :7-12
[8]   CURRENT CONCEPTS Drug-Resistant Epilepsy [J].
Kwan, Patrick ;
Schachter, Steven C. ;
Brodie, Martin J. .
NEW ENGLAND JOURNAL OF MEDICINE, 2011, 365 (10) :919-926
[9]  
Librowski Tadeusz, 2004, Boll Chim Farm, V143, P267
[10]   Flavone and xanthone derivatives related to fluoroquinolones [J].
Mari, S ;
Rossi, M ;
Valenti, P ;
Da Re, P .
FARMACO, 1999, 54 (06) :411-415