PubMed Health⌕ Search

PubMed · 8094257

Differential training sequence effect upon psychostimulant discrimination.

Abstract

1. Previous studies indicate that rats trained to discriminate either cathinone or cathine from its vehicle have a diminished discriminative performance when tested 24 hours after a drug administration when compared to tests conducted after a vehicle administration. The phenomenon of rapid tolerance may occur to produce a lessened interceptive cue on the test day following administration of the drug. It would, therefore, be probable that when rats are trained with consecutive cathinone or cathine administrations they would perform less well than if they were trained with these drugs never given in consecutive training sessions. 2. To test this hypothesis, rats were trained with 0.8 mg/kg 1-cathinone or 4.8 mg/kg d-cathine in a two-lever, food motivated operant task. Each of these groups were divided into two subgroups with the one receiving consecutive drug administrations and the second never receiving two consecutive administrations of the drug. 3. Results indicate that in the cathine-trained group, there was a significant increase in the time that was necessary to train the animals when consecutive administrations were used in training. This, however, did not occur in the cathinone-treated group. There was, however, no significant difference between the differentially trained groups as to ED50 values. 4. It, thus, appears that there may not be a correlative relationship between speed of acquisition, as documented by sessions-to-criterion, and sensitivity, as indicated by ED50 values.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

M D Schechter. 1993. Differential training sequence effect upon psychostimulant discrimination.. https://doi.org/10.1016/0278-5846(93)90051-s

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related citations

Enantioselective total synthesis of (+)-gliocladin C.

The first total synthesis of gliocladin C, a fungal-derived marine alkaloid containing a rare trioxopiperazine fragment, is reported. This asymmetric synthesis establishes the absolute configuration of this structurally novel natural product. [reaction: see text].

Alkaloids↗

Two novel glycosidic triterpene alkaloids from the stem barks of Machilus yaoshansis.

[structure: see text] Two unusual glycosidic triterpene alkaloids, machilaminosides A (1) and B (2), have been isolated from the stem barks of Machilus yaoshansis. Their structures were elucidated by detailed spectroscopic analysis. A possible biogenetic origin of 1 and 2 mediated by the coupling of 2-O-beta-D-glucopyranosyl-cucurbitacin I, respectively, with urea and adenosine was postulated. 1 and 2 showed nonselective cytotoxic activities against several human cancer cell lines as well as TNF-alpha secretion inhibitory activities.

Alkaloids↗

Functional analysis of norcoclaurine synthase in Coptis japonica.

(S)-Norcoclaurine is the entry compound in benzylisoquinoline alkaloid biosynthesis and is produced by the condensation of dopamine and 4-hydroxyphenylacetaldehyde (4-HPAA) by norcoclaurine synthase (NCS) (EC 4.2.1.78). Although cDNA of the pathogenesis-related (PR) 10 family, the translation product of which catalyzes NCS reaction, has been isolated from Thalictrum flavum, its detailed enzymological properties have not yet been characterized. We report here that a distinct cDNA isolated from Coptis japonica (CjNCS1) also catalyzed NCS reaction as well as a PR10 homologue of C. japonica (CjPR10A). Both recombinant proteins stereo-specifically produced (S)-norcoclaurine by the condensation of dopamine and 4-HPAA. Because a CjNCS1 cDNA that encoded 352 amino acids showed sequence similarity to 2-oxoglutarate-dependent dioxygenases of plant origin, we characterized the properties of the native enzyme. Sequence analysis indicated that CjNCS1 only contained a Fe(2+)-binding site and lacked the 2-oxoglutarate-binding domain. In fact, NCS reaction of native NCS isolated from cultured C. japonica cells did not depend on 2-oxoglutarate or oxygen, but did require ferrous ion. On the other hand, CjPR10A showed no specific motif. The addition of o-phenanthroline inhibited NCS reaction of both native NCS and recombinant CjNCS1, but not that of CjPR10A. In addition, native NCS and recombinant CjNCS1 accepted phenylacetaldehyde and 3,4-dihydroxyphenylacetaldehyde, as well as 4-HPAA, for condensation with dopamine, whereas recombinant CjPR10A could use 4-hydroxyphenylpyruvate and pyruvate in addition to the above aldehydes. These results suggested that CjNCS1 is the major NCS in C. japonica, whereas native NCS extracted from cultured C. japonica cells was more active and formed a larger complex compared with recombinant CjNCS1.

Alkaloids↗