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Drug Development Research

ISSN 0272-4391

3 papers in the library · 197 citations · publishing 1983-2007

Papers

Pharmacological profile of ritanserin: A very specific central serotonin S2‐antagonist

Drug Development Research January 1, 1988 F. Awouters, C. J. E. Niemegeers, Anton A. H. P. Megens et al. 139 citations

Ritanserin, a novel methylenepiperidine derivative, acts as a potent, long-lasting, and specific central serotonin S2 antagonist in rats. It inhibits tryptamine-induced cyanosis at 0.0070 mg/kg and bilateral clonic seizures at 0.037 mg/kg, and it blocks mescaline- and 5-HTP-induced head twitches at doses up to 0.11 mg/kg. The compound does not generalize with LSD but weakly antagonizes the LSD discriminative stimulus. It reverses mast cell serotonin cyanosis at 0.012 mg/kg and inhibits gastric lesions at 0.028 mg/kg. Ritanserin shows no central dopamine antagonism or interference with norepinephrine or acetylcholine at doses up to 40 mg/kg. Peripheral histamine antagonism requires 270 times the central S2-antagonism dose.

Mescaline‐induced head‐twitches in the rat: An in vivo method to evaluate serotonin S2 antagonists

Drug Development Research January 1, 1983 C. J. E. Niemegeers, Françis C. Colpaert, J.e. Leysen et al. 58 citations

An intravenous dose of 20.0 mg/kg of mescaline reliably caused head-twitching in rats. Many drugs with different pharmacological actions were tested for their ability to block this response, including numerous serotonin antagonists and two selective S2 antagonists: ketanserin and pirenperone. The same compounds were also examined in six in vivo tests measuring antagonism at serotonin, dopamine, norepinephrine, histamine, or acetylcholine sites. Inhibition of mescaline-induced head-twitches did not correlate with blocking dopamine, norepinephrine, histamine, or acetylcholine receptors, but did correlate with in vivo antagonism of tryptamine and 5-hydroxytryptophan, and with inhibition of 3H-spiperone binding to rat prefrontal cortex in...

Accelerating drug development: Methodology to support first-in-man pharmacokinetic studies by the use of drug candidate microdosing

Drug Development Research February 1, 2007

Microdosing—giving a very small, sub-pharmacological dose of a new chemical entity—allows early evaluation of human pharmacokinetics under an exploratory Investigational New Drug application. This can help select a lead compound, determine the amount of material needed for early development, and set the initial Phase I dose. The pharmaceutical industry has been slow to adopt microdosing because of concerns about analytical sensitivity and possible non-linear pharmacokinetics at low doses. Accelerator mass spectrometry, the usual detection method, is expensive and requires radiolabeling. This report presents an example using LC/MS/MS after microdosing an experimental agent in cynomolgus monkeys.