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  • Oxford University Press (OUP)  (2)
  • Lahlou, Saad  (2)
  • 1
    In: Journal of Pharmacy and Pharmacology, Oxford University Press (OUP), Vol. 64, No. 8 ( 2012-07-09), p. 1155-1164
    Abstract: The effects of rel-(1S,4aS,7S,8aS)-7-(1-vinyl)-tetradecahydro-1,4a-dimethylphenanthrene-7,8a-carbolactone-1-carboxylic acid (TCCA), a new ent-kaurene diterpene isolated from Croton argyrophylloides, on rat tracheal preparations were investigated. Methods Tracheae were removed and cut into two-cartilage segments that were mounted in organ baths containing Tyrode's solution. Results TCCA reduced the contractions induced by electrical field stimulation, relaxed K+-induced contractions, and inhibited both phasic and tonic components of the K+- and ACh-induced contractions. TCCA reduced the serotonin-induced contraction, abolished that evoked by K+ in the presence of epinephrine, and also reduced the ACh-induced contractions under Ca2+-free conditions. TCCA blocked contractions that depend on divalent cation inflow through voltage-operated Ca2+ channels (VOCCs) and receptor-operated Ca2+ channels (ROCCs), but had greater potency to block VOCC- than ROCC-dependent contractions or contractions induced by ACh in Ca2+-free conditions. TCCA relaxed the phorbol 12,13 dibutyrate (1 µm) induced contraction, but with slight potency. Conclusions TCCA induces an antispasmodic effect through several mechanisms including blockade of either VOCCs (with greater potency) or ROCCs, blockade of IP3-induced Ca2+ release from sarcoplasmic reticulum (with intermediate potency) and reduction of the sensitivity of contractile proteins to Ca2+.
    Type of Medium: Online Resource
    ISSN: 2042-7158 , 0022-3573
    Language: English
    Publisher: Oxford University Press (OUP)
    Publication Date: 2012
    detail.hit.zdb_id: 2041988-0
    detail.hit.zdb_id: 2050532-2
    SSG: 15,3
    Location Call Number Limitation Availability
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  • 2
    Online Resource
    Online Resource
    Oxford University Press (OUP) ; 2010
    In:  Journal of Pharmacy and Pharmacology Vol. 62, No. 8 ( 2010-07-21), p. 1045-1053
    In: Journal of Pharmacy and Pharmacology, Oxford University Press (OUP), Vol. 62, No. 8 ( 2010-07-21), p. 1045-1053
    Abstract: Croton nepetaefolius is a medicinal plant useful against intestinal disorders. In this study, we elucidate the effects of its essential oil (EOCN) on sympathetic neurons, with emphasis on the interaction of EOCN- and histamine-induced effects. Methods The effects of EOCN and histamine were studied in guinea-pig celiac ganglion in vitro. Key findings Histamine significantly altered the resting potential (Em) and the input resistance (Ri) of phasic neurons (from −56.6 ± 1.78 mV and 88.6 ± 11.43 MΩ, to −52.9 ± 1.96 mV and 108.6 ± 11.00 MΩ, respectively). Em, Ri and the histamine-induced alterations of these parameters were not affected by 200 µg/ml EOCN. The number of action potentials produced by a 1-s (two-times threshold) depolarising current and the current threshold (Ith) for eliciting action potentials (rheobase) were evaluated. Number of action potentials and Ith were altered by histamine (from 2.6 ± 0.43 action potentials and 105.4 ± 11.15 pA to 6.2 ± 1.16 action potentials and 67.3 ± 8.21 pA, respectively). EOCN alone did not affect number of action potentials and Ith but it fully blocked the histamine-induced modifications of number of action potentials and Ith. All the effects produced by histamine were abolished by pyrilamine. Conclusions EOCN selectively blocked histamine-induced modulation of active membrane properties.
    Type of Medium: Online Resource
    ISSN: 0022-3573 , 2042-7158
    Language: English
    Publisher: Oxford University Press (OUP)
    Publication Date: 2010
    detail.hit.zdb_id: 2041988-0
    detail.hit.zdb_id: 2050532-2
    SSG: 15,3
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
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