Volume 11, Issue 3 (September 2024)                   Avicenna J Neuro Psycho Physiology 2024, 11(3): 125-131 | Back to browse issues page

XML Print


Download citation:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:

Ionov I, Krasilova M, Pushinskaya I, Gorev N, Tulchinskiy V, Gabov S. Synergy of somatostatin – substance P receptors antagonists in the initiation of catalepsy in rats. Avicenna J Neuro Psycho Physiology 2024; 11 (3) :125-131
URL: http://ajnpp.umsha.ac.ir/article-1-486-en.html
1- 1 Head, Department of Neurometabolic Analysis, Centre on Theoretical Problems in Physical and Chemical Pharmacology, Russian Academy of Sciences, Moscow, 109029, Russia , newrology@yandex.ru
2- Senior Researcher, Department of Neurometabolic Analysis, Centre on Theoretical Problems in Physical and Chemical Pharmacology, Russian Academy of Sciences, Moscow, 109029, Russia
3- Researcher, Department of Neurometabolic Analysis, Centre on Theoretical Problems in Physical and Chemical Pharmacology, Russian Academy of Sciences, Moscow, 109029, Russia
4- Senior Technical Expert, Timpharm LTD, Moscow, 117513, Russia
Abstract:   (335 Views)
The parkinsonian brain undergoes a decrease in  levels of somatostatin (SST) and substance P (SP). According to previous studies, brain SST deficit in rats simulated by i.c.v. injections of SST receptor antagonist, cyclosomatostatin (cSST), increases the speed of catalepsy development. Nevertheless, it is not clear how the SP, a natural ligand of neurokinin-1 (NK1) receptors, contributes to the growth of catalepsy.
The present study aimed to find out whether simultaneous blockade of central somatostatin and NK1 receptors can lead to catalepsy, a model for parkinsonian bradykinesia and rigidity. The experiments were conducted on Wistar rats. The blockade of somatostatin and NK1 receptors was simulated by intracerebroventricular injections of cSST and substance L-733,060,  respectively. Bar test was used to evaluate the catalepsy. No catalepsy was induced by cSST at 1.0 µg  and  L-733,060 at 10.0 ng injected separately. Nevertheless, co-administration of these agents led to a clear cataleptic response. Cataleptogenic action  of the combination was reversed by SP. Based on such results, cSST and L-733,060 can synergistically induce catalepsy in the rat. According to these findings, Parkinson’s disease-associated  brain deficit in SST and SP could be relevant for pathogenesis of  extrapyramidal dysfunctions. Considering the aforementioned findings, the processes mediated by central SST  and NK1 receptors could be possible therapeutic targets for parkinsonism.
     
Article Type: Research Article | Subject: Movement disorders
Received: 2024/05/17 | Accepted: 2024/09/20 | Published: 2025/02/24

Add your comments about this article : Your username or Email:
CAPTCHA

Send email to the article author


Rights and permissions
Creative Commons License This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.

© 2025 CC BY 4.0 | Avicenna Journal of Neuro Psycho Physiology

Designed & Developed by : Yektaweb