The previous study showed that chronic treatment with Withania somnifera extract (WS) inhibited haloperidol-induced catalepsy. It is suggested that caffeine and WS may be useful adjuvants in pharmacotherapy of Parkinson's disease. There are no studies on the effect of haloperidol on mice withdrawn from caffeine or W. somnifera. We therefore studied the effect of a single administration of standardised WS containing 5.1% total withanolides (WS, 30 or 100 mg kg(-1) i.p.) and/or caffeine (3 mg kg(-1) i.p.) and withdrawal from 6 days treatment with WS and/or caffeine, on haloperidol-induced catalepsy in albino mice. Single administration of both WS and caffeine, used either alone or in combination, significantly inhibited catalepsy. Mice withdrawn from caffeine significantly inhibited haloperidol-induced catalepsy, but mice withdrawn from WS showed increased catalepsy. The study indicated that withdrawal from WS does not retain anticataleptic activity, and caffeine but not WS may be a good adjuvant in pharmacotherapy of Parkinson's disease.

Download full-text PDF

Source
http://dx.doi.org/10.1080/14786410802346215DOI Listing

Publication Analysis

Top Keywords

haloperidol-induced catalepsy
16
catalepsy mice
12
mice withdrawn
12
caffeine
8
anticataleptic activity
8
withania somnifera
8
inhibited haloperidol-induced
8
pharmacotherapy parkinson's
8
parkinson's disease
8
withdrawn caffeine
8

Similar Publications

Objective: Acetylcholine modulates the activity of the direct and indirect pathways within the striatum through interaction with muscarinic M and M receptors. M receptors are uniquely positioned to regulate plasticity within the direct pathway and play a substantial role in reward and addiction-related behaviors. However, the role of M receptors on cholinergic neurons has been less explored.

View Article and Find Full Text PDF

Background/objectives: Antipsychotic medicines are used to treat several psychological disorders and some symptoms caused by dementia and schizophrenia. Haloperidol (Hal) is a typical antipsychotic usually used to treat psychosis; however, its use causes motor or extrapyramidal symptoms (EPS) such as catalepsy. Hal blocks the function of presynaptic D2 receptors on cholinergic interneurons, leading to the release of acetylcholine (ACh), which is hydrolyzed by the enzyme acetylcholinesterase (AChE).

View Article and Find Full Text PDF

Clavulanic acid (ClvA), a beta-lactamase inhibitor, is being explored for its significant neuroprotective potential. The effects of ClvA were assessed both individually and in combination with crocin (Cr), an antioxidant derived from saffron, in the context of tardive dyskinesia (TD). In rat haloperidol (Hp)-induced-TD (1 mg/kg, i.

View Article and Find Full Text PDF

Opposite regulation by L-DOPA receptor GPR143 of the long and short forms of the dopamine D2 receptors.

J Pharmacol Sci

October 2024

Department of Molecular Pharmacology and Neurobiology, Yokohama City University Graduate School of Medicine, 3-9 Fukuura, Kanazawa-ku, Yokohama, 236-0004, Japan. Electronic address:

Article Synopsis
  • Dopamine D2 receptors (D2Rs) exist in two isoforms, D2L (long form) primarily in postsynaptic locations, and D2S (short form) mainly acting as presynaptic autoreceptors.
  • L-DOPA enhances the function of D2L by interacting with GPR143, which was initially linked to ocular albinism, showing that GPR143 affects D2L and D2S oppositely.
  • Experiments on mice lacking Gpr143 showed reduced catalepsy from haloperidol and increased dopamine release in the striatum, indicating that GPR143 modulates D2 receptor signaling differently based on the specific isoform involved.
View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!