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  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    BJOG 77 (1970), S. 0 
    ISSN: 1471-0528
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Gastric emptying was measured in non-pregnant, pregnant and labouring women.The results suggest an explanation for previously conflicting studies and support the suggestion that slowing of gastric emptying contributes to heartburn in pregnancy. However, there was no clear evidence that in pregnant women generally gastric emptying is impaired.Gastric emptying times during labour were shown to be prolonged and the pattern of emptying altered.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Annals of the New York Academy of Sciences 713 (1994), S. 0 
    ISSN: 1749-6632
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Natural Sciences in General
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Inflammation research 38 (1993), S. 55-59 
    ISSN: 1420-908X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The effects of either substance P (SP) or a metabolically stable SP analogue, [pGlu5, Me-Phe8, Sar9]SP(5–11), alone or in combination with calcitonin gene-related peptide (CGRP) on blood pressure (BP) and extravasation of serum albumin were examined in normal and diabetic rats. CGRP (12 ng/kg) modified neither BP nor vascular permeability in control and diabetic rats. Both SP and its analogue (74 ng/kg) produced hypotension, and increased plasma extravasation in the respiratory tissues, urinary bladder and skin. The simultaneous injection of CGRP and SP resulted in modest potentiation of the vascular permeability actions of SP in control and diabetic rats. However, extravasatio induced by [pGlu5,Me-Phe8,Sar9]SP(5–11) was potentiated by CGRP in control animals, but not in diabetic rats. Defective neurogenic inflammatory responses in diabetic rats may result from decreased responses in the effector tissues of diabetic rats to the neuropeptides released from sensory nerves.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Digestive diseases and sciences 36 (1991), S. 1574-1581 
    ISSN: 1573-2568
    Keywords: mucin ; intestine ; secretion ; diabetes ; adrenergic ; cholinergic ; cholera toxin
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract In diabetic rats, intestinal mucin secretion is unusually high compared with that in normal rats. These studies demonstrate that mucin synthesis is also increased in the diabetic intestine. α- and β-adrenergic agonists or antagonists did not affect mucin output in either normal or diabetic animals, suggesting that altered release in diabetes was not due to goblet cells responding abnormally to adrenergic agents. The cholinergic agonist bethanechol caused a dose-dependent and atropine-sensitive increase in mucin secretion from the normal intestine but had no effect on mucin release from diabetic tissue. Atropine alone did not reduce mucin secretion from the diabetic intestine to levels found in normal tissue. Cholera toxin caused an approximately fivefold increase in mucin output from normal rats but had no effect on mucin secretion from diabetic animals. Thus, goblet cell responses to cholinergic stimulation and cholera toxin in the diabetic intestine are markedly impaired. However, loss of cholinergic control does not appear to be responsible for altered baseline mucin secretion in diabetes.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 348 (1993), S. 638-642 
    ISSN: 1432-1912
    Keywords: Guanethidine ; Rat ; Capsaicin ; Primary afferent nerves ; Nippostrongylus brasiliensis ; Ruthenium red
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Superfusion of capsaicin onto the serosal surface of jejunum of Nippostrongylus brasiliensis-sensitized rats induces a short-lasting (1–3 min), dose-dependent (2 to 20 μg) decrease in blood pressure which ranges from −5.3±1.40% to −22.6±2.20%. The hypotension evoked by capsaicin was more marked in sensitized rats than in unsensitized animals, which responded only to the highest dose (20 mg) of capsaicin tested. The hypotensive effects of capsaicin were not affected by intravenous injections of mepyramine (10 mg/kg), a histamine receptor antagonist, or by the cycloxygenase inhibitor indomethacin (10 mg/kg). However, an intravenous injection of a platelet-activating factor (PAT) antagonist, BN 52021 (20 mg/kg), or an intraperitoneal injection of guanethidine (8 mg/kg) 18 h prior to experimentation, to functionally impair the sympathetic nerves, abolished the capsaicin-induced drop in blood pressure. Treatment of neonatal rats with capsaicin reduced by 75% the hypotensive effects of capsaicin, whereas the capsaicin antagonist, ruthenium red, reduced non-significantly the hypotensive action of capsaicin. It is concluded that the activation of jejunal sensory nerves in N. brasiliensis-sensitized rats by capsaicin induced a reflex hypotension that is dependent upon PAF release from mast cells and functional sympathetic nerves. In addition, the afferent function of the sensory nerves are not totally blocked by ruthenium red as capsaicin elicits the reflex hypotension in the presence of this blocker of sensory nerve efferent function.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Digestive diseases and sciences 42 (1997), S. 2378-2383 
    ISSN: 1573-2568
    Keywords: FOOD ALLERGY ; IMMEDIATE HYPERSENSITIVITY ; MIGRATING MYOELECTRIC COMPLEXES ; SALIVARY GLANDS
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract A novel peptide, submandibular gland peptide-T(SGP-T), which reduces allergen-induced hypotension, wasexamined for effects on intestinal anaphylaxis.Hooded-Lister rats were sensitized to egg albumin and prepared for the measurement of in vivomyoelectric activity of the jejunum. The disruption ofmigrating myoelectric complexes (MMCs) that occurs uponintraluminal, duodenal challenge with antigen of sensitized rats was inhibited by 75% uponintravenous treatment with 100 μg/kg of SGP-T. Inaddition, SGP-T reduced the number of rats experiencinganaphylactic diarrhea and disrupted MMCs, but thepeptide did not alter antigen-provoked release of ratmast cell protease II. The mechanism of action of SGP-Tremains to be determined, but it apparently does not actdirectly on mast cells to exert its antianaphylactic action. These results emphasize that modulationof immediate hypersensitivity reactions is only one ofseveral gastrointestinal activities that are affected bygrowth factors and peptides released from salivary glands.
    Type of Medium: Electronic Resource
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