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Stjernström Ne

Bio: Stjernström Ne is an academic researcher from Astra. The author has contributed to research in topics: Methyl group & Antidepressant. The author has an hindex of 5, co-authored 17 publications receiving 63 citations.

Papers
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Patent
Carnmalm B1, Tomas de Paulis1, Svante B. Ross1, Rämsby S1, Stjernström Ne1, Sven-Ove Ögren1 
27 Dec 1974
TL;DR: In this paper, the authors present a list of compounds of the formula "STR1" and pharmaceutically acceptable salts thereof; processes for their preparation; intermediates useful for their extraction; pharmaceutical preparations containing at least one of these compounds; and the use thereof as a tranquilizing or neuroleptic agent.
Abstract: Compounds of the formula ##STR1## and pharmaceutically acceptable salts thereof; processes for their preparation; intermediates useful for their preparation; pharmaceutical preparations containing at least one of these compounds; and the use thereof as a tranquilizing or neuroleptic agent

5 citations


Cited by
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Journal ArticleDOI
Svante B. Ross1, A. L. Renyi1
TL;DR: The role of protein binding and diffusion barriers in the causation of the difference in the results obtained with the two preparations is discussed.
Abstract: The simultaneous uptake of 3-H-l-noradrenaline (NA) and 14-C-5-hydroxytryptamine (5-HT) in slices from the midbrain-hypothalamus region of the rat brain was compared with the corresponding uptake in crude synaptosome preparations of the same brain region. In both preparations the uptake of the two amines was selective at the concentration used (1 times 10- minus 7 M or lower). The KM values for the amines (NA: 2 times 10- minus 7 M in synaptosomes and 5 times 10- minus 7 M in slices; 5-HT: 8 times 10- minus 8 M in synaptosomes and 6 times 10- minus 7 M in slices) and the inhibitory concentrations (IC50) of the antidepressant agents were lower in the synaptosome experiments than in the slices experiments. Moreover the order of the inhibitory activities differed between the two preparations. In the slices experiments the NA uptake was inhibited most markedly by desipramine followed by imipramine greater than chlorimipramine = nortriptyline greater than or equal to amitriptyline greater than or equal to chlordesipramine whereas in the synaptosome experiments the order was desipramine greater than nortriptyline greater than or equal to chlordesipramine greater than or equal to imipramine greater than amitriptyline greater than or equal to chlorimipramine. For the 5-HT uptake in slices the order of activity was: chlorimipramine greater than imipramine greater than or equal to amitriptyline greater than or equal to chlordesipramine = desipramine greater than or equal to nortriptyline whereas in the synaptosome preparations the order was: chlorimipramine greater than imipramine greater than or equal to amitriptyline greater than or equal to chlordesipramine greater than nortriptyline = desipramine. The role of protein binding and diffusion barriers in the causation of the difference in the results obtained with the two preparations is discussed.

198 citations

Journal ArticleDOI
TL;DR: The study of drug-induced changes in body temperature has expanded greatly within the past decade and the cited literature is a readily available source of information on interactions between certain drugs and the thermoregulatory system.

196 citations

Journal ArticleDOI
Svante B. Ross1, A. L. Renyi1
TL;DR: It was found that H was rapidly transformed to A 24356 in vivo and that the main effect in vivo was caused by the secondary amine derivative.

167 citations

Journal ArticleDOI
TL;DR: This survey, the second in a series, presents extensive tabulations of literature on thermoregulatory effects of cholinergic agonists and antagonists, histamine and H1- and H2-receptor antagonists, narcotic analgesics and antagonists in both non-tolerant and tolerant subjects and of prostaglandins and related agents.

167 citations

Journal ArticleDOI
TL;DR: The ratio between the degree of alkylation of DNA in various organs and of hemoglobin was approximately the same, supporting a previous conclusion that ethene oxide is the reactive intermediate formed in vivo from e thene.

164 citations