21 research outputs found
Plasmapheresis in the treatment of myasthenia gravis: retrospective study of 26 patients
Glaucoma correlates with increased risk of Parkinson’s disease in the elderly: a national-based cohort study in Taiwan
Repeated visual hallucinations in Parkinson's disease as disturbed external/internal perceptions: Focused review and a new integrative model
L-Type Cav1.2 Calcium Channel is Involved in 6-Hydroxydopamine-Induced Neurotoxicity in Rats
Behavioural Assessment of the A2a/NR2B Combination in the Unilateral 6-OHDA-Lesioned Rat Model: A New Method to Examine the Therapeutic Potential of Non-Dopaminergic Drugs
Antiparkinsonian Effects of Aqueous Methanolic Extract of Hyoscyamus niger Seeds Result From its Monoamine Oxidase Inhibitory and Hydroxyl Radical Scavenging Potency
Hyoscyamus species is one of the four plants
used in Ayurveda for the treatment of Parkinson’s disease
(PD). Since Hyoscyamus niger was found to contain negligible
levels of L-DOPA, we evaluated neuroprotective
potential, if any, of characterized petroleum ether and
aqueous methanol extracts of its seeds in 1-methyl-4-phenyl-
1,2,3,6-tetrahydropyridine (MPTP) model of PD in
mice. Air dried authenticated H. niger seeds were
sequentially extracted using petroleum ether and aqueous
methanol and were characterized employing HPLC-electrochemistry
and LCMS. Parkinsonian mice were treated
daily twice with the extracts (125–500 mg/kg, p.o.) for two
days and motor functions and striatal dopamine levels were
assayed. Administration of the aqueous methanol extract
(containing 0.03% w/w of L-DOPA), but not petroleum ether extract, significantly attenuated motor disabilities
(akinesia, catalepsy and reduced swim score) and striatal
dopamine loss in MPTP treated mice. Since the extract
caused significant inhibition of monoamine oxidase activity
and attenuated 1-methyl-4-phenyl pyridinium (MPP?)-
induced hydroxyl radical (�OH) generation in isolated
mitochondria, it is possible that the methanolic extract of
Hyoscyamus niger seeds protects against parkinsonism in
mice by means of its ability to inhibit increased �OH
generated in the mitochondria
