ritanserin has been researched along with Anochlesia in 8 studies
Ritanserin: A selective and potent serotonin-2 antagonist that is effective in the treatment of a variety of syndromes related to anxiety and depression. The drug also improves the subjective quality of sleep and decreases portal pressure.
ritanserin : A thiazolopyrimidine that is 5H-[1,3]thiazolo[3,2-a]pyrimidin-5-one which is substituted at position 7 by a methyl group and at position 6 by a 2-{4-[bis(4-fluorophenyl)methylidene]piperidin-1-yl}ethyl group. A potent and long-acting seratonin (5-hydroxytryptamine, 5-HT) antagonist of the subtype 5-HT2 (Ki = 0.39 nM), it is used in the treatment of a variety of disorders including anxiety, depression and schizophrenia. It has little sedative action.
Excerpt | Relevance | Reference |
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"Catalepsy was defined as rats remaining immobile over a horizontal metal bar for at least 30 s, 90 min after dosing." | 1.30 | Attenuation of haloperidol-induced catalepsy by a 5-HT2C receptor antagonist. ( Blackburn, TP; Holland, V; Kettle, A; Reavill, C; Riley, G, 1999) |
"In this study, both catalepsy and changes in extracellular levels of striatal dopamine (DA) and dihydroxyphenyl acetic acid (DOPAC) induced by the typical neuroleptic haloperidol (HAL) were simultaneously assessed, using intracerebral microdialysis in freely moving rats, in the presence of either the 5-HT1A agonist 8-OH-DPAT or the 5-HT2A/C antagonist ritanserin." | 1.30 | 8-OH-DPAT, a 5-HT1A agonist and ritanserin, a 5-HT2A/C antagonist, reverse haloperidol-induced catalepsy in rats independently of striatal dopamine release. ( Bonhomme, N; De Deurwaerdère, P; Le Moal, M; Lucas, G; Spampinato, U, 1997) |
"120 min)." | 1.28 | Antagonism by 8-OH-DPAT, but not ritanserin, of catalepsy induced by SCH 23390 in the rat. ( Wadenberg, ML, 1992) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 7 (87.50) | 18.2507 |
2000's | 1 (12.50) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Reavill, C | 1 |
Kettle, A | 1 |
Holland, V | 1 |
Riley, G | 1 |
Blackburn, TP | 1 |
Chang, PY | 1 |
Chuang, CH | 1 |
Chen, JC | 1 |
Tung, CS | 1 |
Kulikov, AV | 2 |
Kolpakov, VG | 1 |
Maslova, GB | 1 |
Kozintsev, I | 1 |
Popova, NK | 2 |
Wadenberg, ML | 2 |
Ahlenius, S | 1 |
Lucas, G | 1 |
Bonhomme, N | 1 |
De Deurwaerdère, P | 1 |
Le Moal, M | 1 |
Spampinato, U | 1 |
Nucci-da-Silva, LP | 1 |
Guimarães, FS | 1 |
Del Bel, EA | 1 |
Barykina, NN | 1 |
Alekhina, TA | 1 |
Naumenko, KS | 1 |
8 other studies available for ritanserin and Anochlesia
Article | Year |
---|---|
Attenuation of haloperidol-induced catalepsy by a 5-HT2C receptor antagonist.
Topics: Animals; Binding, Competitive; Catalepsy; Cell Line; Dopamine Antagonists; Fluorobenzenes; Haloperid | 1999 |
Behavioral and biochemical effects of amperozide and serotonin agents on nigrostriatal and mesolimbic dopamine systems.
Topics: Amphetamines; Animals; Behavior, Animal; Catalepsy; Corpus Striatum; Dopamine; Haloperidol; Limbic S | 2008 |
Effect of selective 5-HT1A agonists and 5-HT2 antagonists on inherited catalepsy in rats.
Topics: 8-Hydroxy-2-(di-n-propylamino)tetralin; Animals; Behavior, Animal; Catalepsy; Dose-Response Relation | 1994 |
Antagonism by the 5-HT2A/C receptor agonist DOI of raclopride-induced catalepsy in the rat.
Topics: 5-Hydroxytryptophan; Amphetamines; Animals; Benserazide; Benzazepines; Catalepsy; Dopamine Agents; D | 1995 |
8-OH-DPAT, a 5-HT1A agonist and ritanserin, a 5-HT2A/C antagonist, reverse haloperidol-induced catalepsy in rats independently of striatal dopamine release.
Topics: 8-Hydroxy-2-(di-n-propylamino)tetralin; Animals; Catalepsy; Dopamine; Haloperidol; Male; Rats; Rats, | 1997 |
Serotonin modulation of catalepsy induced by N(G)-nitro-L-arginine in mice.
Topics: Adrenergic alpha-Antagonists; Animals; Bridged Bicyclo Compounds, Heterocyclic; Catalepsy; Dose-Resp | 1999 |
[Effect of 5HT2 receptor blockade on the startle reflex and its prepulse inhibition in mice and rats of various strains].
Topics: Animals; Catalepsy; Cyproheptadine; Ketanserin; Mice; Mice, Inbred CBA; Rats; Rats, Wistar; Receptor | 1999 |
Antagonism by 8-OH-DPAT, but not ritanserin, of catalepsy induced by SCH 23390 in the rat.
Topics: 8-Hydroxy-2-(di-n-propylamino)tetralin; Animals; Avoidance Learning; Benzazepines; Catalepsy; Dopami | 1992 |