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- IRMS - Nicolae Testemitanu SUMPh
- REVISTE MEDICALE NEINSTITUȚIONALE
- The Moldovan Medical Journal
- Curierul Medical 2009 - 2016
- Curierul Medical, 2014
- Curierul Medical, 2014, Vol. 57, Nr. 3
Please use this identifier to cite or link to this item:
http://hdl.handle.net/20.500.12710/7358
Title: | Нейрофармакологическое изучение эффектов диуманкала и декурсинола – антагонистов кальция нового поколения |
Other Titles: | The neuropharmacological study of diumancal and decursinol – a new generation of calcium antagonists |
Authors: | Abdullayeva, Rena Agaev, E. |
Keywords: | diumancal;decursinol;behavioral activity;catecholaminergic system;lipid peroxidation |
Issue Date: | 2014 |
Publisher: | The Scientific Medical Association of the Republic of Moldova |
Citation: | ABDULLAYEVA, R.; AGAEV, E. Нейрофармакологическое изучение эффектов диуманкала и декурсинола –антагонистов кальция нового поколения. In: Curierul Medical. 2014, vol. 57, no 3, pp. 48-53. ISSN 1875-0666. |
Abstract: | Background: The present study investigated the influence of diumancal and decursinol on the level of monoamines and products of lipid peroxidation
within the different brain structures (hypothalamus, frontal cortex, striatum) and the importance of presynaptic and postsynaptic parts of catecholaminergic
system of the brain in their mechanism of action.
Material and methods: The study was conducted on 520 white male rats, 150-220 g weight. The substances were administered intraperitoneally in the
following dosages: diumancal – 0.1 mg/kg; 0.5 mg/kg; 1 mg/kg; decursinol – 1 mg/ kg; 5 mg/kg; 10 mg/kg and verapamil – 5 mg/kg; 15 mg/kg.
Results: The study revealed that diumancal and decursinol have dose dependent, two-phase action: in low dosage they activate, while in high dosage they
suppress behavioral activity of rats. The use of pharmacological analyzers (cлонидин 0.05 мг/кg, апоморфин 0.1 mg/kg; 1 мг/кg, a-methyltyrosine 200
мг/кg, propranolol 15 м/кg) allowed to reveal the importance of pre- and postsynaptic catecholaminergic mechanisms of the brain in the mechanism of
action of diumancal and decursinol. During trials both drugs increased serotonin level in hypothalamus, corpus striatum and frontal cortex, decreased
norepinephrine in hypothalamus and frontal cortex and dopamine in corpus striatum. The level of dopamine in hypothalamus and frontal cortex
decreased after administration of low doses of diumancal and decursinol and did not change under the influence of high doses.
Conclusions: Diumancal and decursinol decrease the formation of products of lipid per oxidation, increased during stress, and possibly have antioxidant
action. |
metadata.dc.relation.ispartof: | Curierul Medical |
URI: | http://repository.usmf.md/handle/20.500.12710/7358 http://moldmedjournal.md/wp-content/uploads/2016/09/Cm-3-57-Electornic-PDF-version.pdf |
ISSN: | 1857-0666 |
Appears in Collections: | Curierul Medical, 2014, Vol. 57, Nr. 3
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