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  • 1
    ISSN: 1553-3840
    Source: Berkeley Electronic Press Academic Journals
    Topics: Medicine
    Notes: Natural health products containing Echinacea have been used by many patient populations and although there are reports of adverse effects with products containing Echinacea, few clearly characterized the nature of the product with respect to constituent content, the nature of the products and the mechanism underlying the interaction. The objective of this study was to examine blended and single-entity Echinacea products containing ground plant material or extracts in commercial capsules, herbal teas, tablets, tinctures and soft gel liquid-filled capsule formulations in an attempt to correlate biomarker constituent content and effects on cellular and subcellular parameters of interest. HPLC analysis indicated significant variability in the major biomarker constituent content in extracts from these Echinacea products. These extracts were also examined for their potential to affect cytochrome P450 CYP1A1/2, 2C9*1, 2C9*2, 2C19, 2D6, 3A4, 3A5, 3A7, and flavin-containing monooxygenase 3 (FMO3); CYP3A5-mediated metabolism, and expression of CYP3A4 and ABCB1. The extracts of some products were also examined for their effect cellular processes such as cell proliferation, nitric oxide formation as a marker of immunostimulatory capacity, and lactate dehydrogenase release as a marker for cell toxicity. The present study indicated that key Echinacea constituents varied widely within and between the products tested and that these levels did not correlate with the ability of these products to markedly affect the cellular processes studied.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 338 (1988), S. 287-292 
    ISSN: 1432-1912
    Keywords: PYY ; Rat ; Non-adrenergic ; Non-cholinergic ; In vitro ; Small intestine
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The effects of peptide YY (PYY) on motor activity of the rat small intestine, were studied using isolated organ bath preparations arranged for recording muscle activity in the longitudinal axis. PYY induced TTX sensitive concentration-dependent contractions and/or relaxations of the longitudinal muscle in different regions of the small intestine. In the duodenum PYY evoked only “cholinergic” contractions (3 × 10−8−3 × 10−7 M). In the jejunum, PYY-evoked concentrations were non-cholinergic, and contractions were never seen in the ileum. In the jejunum and ileum, PYY-evoked relaxations (3 × 10−3 × 10−7 M) were unaffected by adrenoceptor or cholinergic receptor blockade, thus indicating that these relaxations were mediated by non-adrenergic, non-cholinergic (NANC) inhibitory nerves. Another action of PYY was to cause inhibition of field stimulation-evoked cholinergic concentrations. This inhibitory action was primarily due to antagonism of post-junctional, cholinergic receptor mediated events. In addition, PYY inhibited histamine evoked contractions of the longitudinal muscle. All regions of the small intestine could be desensitized to PYY. Such PYY-densensitization did not affect the ability of the longitudinal muscle to relax in response to applied ATP or papaverine. These results suggest PYY has potent concentration-dependent stimulatory actions at intrinsic inhibitory and excitatory motor nerves. In addition, PYY interferes with contractions but not relaxations of the longitudinal muscle.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Digestive diseases and sciences 34 (1989), S. 1211-1216 
    ISSN: 1573-2568
    Keywords: γ-aminobutyric acid ; GABA ; cysteamine HCl ; duodenal ulcer ; rat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Subcutaneous administration of a single dose of γ-aminobutyric acid (GABA, 10 mg/100 g) in conjunction with a pretreatment dose of aminooxyacetic acid (AOAA 2.5 mg/100 g subcutaneously) to prevent the degradation of GABA, significantly augmented the incidence and intensity of cysteamine HCl-induced duodenal ulceration in rats. This effect of GABA could be reduced by the GABA receptor antagonist, bicuculline (30 Μg/100 g subcutaneously). These results suggest peripheral GABA receptors can modulate cysteamine HCl-induced duodenal ulcer.
    Type of Medium: Electronic Resource
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