Passiflora caerulea L. fruit extract and its metabolites ameliorate epileptic seizure, cognitive deficit and oxidative stress in pilocarpine-induced epileptic mice

被引:26
作者
Aseervatham, G. Smilin Bell [1 ,2 ]
Abbirami, E. [3 ]
Sivasudha, T. [3 ]
Ruckmani, K. [1 ,4 ]
机构
[1] Anna Univ, Ctr Excellence Nanobio Translat REs Ctr, Natl Facil Drug Dev Acad Pharmaceut & Allied Ind, BIT Campus, Tiruchirappalli 620024, Tamil Nadu, India
[2] Bharathidasan Univ, Holy Cross Coll Autonomous, PG & Res Dept Biotechnol & Bioinformat, Tiruchirappalli 620002, Tamil Nadu, India
[3] Bharathidasan Univ, Dept Environm Biotechnol, Tiruchirappalli 620024, Tamil Nadu, India
[4] Anna Univ, Dept Pharmaceut Technol, BIT Campus, Tiruchirappalli 620024, Tamil Nadu, India
关键词
Epilepsy; Passiflora caerulea; Antioxidant; Hippocampus; Y-maze; ANTIOXIDANT ACTIVITY; ELECTRICAL-STIMULATION; PHENOLIC-COMPOUNDS; BRAIN; FLAVONOIDS; MEMORY; PLANTS; POLYPHENOLS; NARINGENIN; MECHANISMS;
D O I
10.1007/s11011-019-00501-5
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The anticonvulsant potential of aqueous fruit extract of Passiflora caerulea (PCAE) was evaluated in swiss albino mice induced by pilocarpine. The antioxidant activities of PCAE were determined which showed strong antioxidant activity and the polyphenol compounds such as ginsenoside, naringenin, chrysoeriol 8-c-glucoside, luteolin-6-C-glucoside, apigenin-6,8-di-C-beta-D-glucopyranoside were profiled through RP-HPLC and UPLC-ESI-MS/MS. Chronic effects of PCAE on pilocarpine (85 mg/kg; i.p)-induced convulsions were evaluated in Swiss adult male albino mice. PCAE at 100 and 200 mg/kg, (p.o.) and diazepam (5 mg/kg, i.p) were administered once daily for 15 days. In Y-maze test, percentage of correct entry by pilocarpine administered animals were significantly lower when compared to control, whereas PCAE at both doses improved the alteration score significantly. Administration of higher dose (200 mg/kg) of PCAE significantly delayed onset of convulsions and decreased duration of clonic convulsions. Association of ROS production during seizure period was further confirmed by histopathological studies revealing loss of normal neuronal cells in hippocampus region. The data obtained showed anticonvulsant activity and improved cognitive function; reduced the oxidative damage and significantly activated the cholinergic neurotransmission in a dose dependent manner similar to diazepam which is evident in the biochemical parameters and histopathological study, suggesting therapeutic potential for epilepsy and neurodegeneration.
引用
收藏
页码:159 / 173
页数:15
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