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  • 11
    ISSN: 1433-8580
    Keywords: H2-Receptor ; Somatostatin ; Pancreatic polypeptide ; Gastrin ; Insulin
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The effect of histamine H2-receptor stimulation via the infusion of impromidine was assessed with regard to postprandial plasma insulin, pancreatic polypeptide (PP), somatostatin, and gastrin levels. The effect of impromidine was assessed in the postprandial state during a liver extract/sucrose test meal which had a buffer capacity to maintain the intragastric pH at a constant level for the time impromidine was infused. Postprandial plasma insulin and gastrin levels were not changed by impromidine (10µg/kg·h−1). Plasma somatostatin levels rose significantly, whereas the postprandial increase of plasma PP levels was attenuated. The effects on somatostatin and PP were antagonized by the infusion of cimetidine, a specific histamine H2-receptor blocker. In conclusion the present data demonstrate that in the postprandial state activation of H2-receptors stimulates somatostatin and inhibits PP release while insulin and gastrin release are not affected.
    Type of Medium: Electronic Resource
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  • 12
    Electronic Resource
    Electronic Resource
    Springer
    Research in experimental medicine 180 (1982), S. 223-228 
    ISSN: 1433-8580
    Keywords: Synthetic human gastrin I ; Gastrin-like pentapeptide ; Intestinal absorption ; Zollinger-Ellison syndrome
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The effects of synthetic human gastric I (SHG I) and gastrin-like pentapeptide (PG) on jejunal water, electrolyte, and glucose absorption were studied in 11 normal subjects. The i.v. administration of graded doses of SHG I increased plasma gastrin levels similar to those after food intake and in the Zollinger-Ellison syndrome. SHG I and PG caused no significant changes in the net movement of water and solute. The findings indicate that gastrin has no direct effect on intestinal absorption in normal man, and does not account for the mechanism of diarrhea in the Zollinger-Ellison syndrome.
    Type of Medium: Electronic Resource
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  • 13
    ISSN: 1432-0428
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 14
    ISSN: 1432-0428
    Keywords: β-Casomorphin ; enkephalin ; naloxone ; insulin release ; exorphins ; opiates ; dog
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary We have previously demonstrated that opiate-like substances in food protein (exorphins), contained in the peptic digest of gluten, stimulate insulin and glucagon release in dogs and that this effect is inhibited by the opiate antagonist naloxone. The present study was designed to evaluate the possible rôle of ingested opiate-like substances in the modulation of post-prandial insulin release. Similarly, the addition of synthetic β-casomorphins, which are the opioid-active material of bovine casein peptone, elicit a stimulation of post-prandial insulin release during a liver extract-sucrose test meal. The addition of met-enkephalin to a liver extract-sucrose test meal also augmented the post-prandial insulin response. Both stimulatory effects were reversed by oral naloxone, as was the post-prandial increase of insulin following ingestion of bovine casein peptone (casopeptone). The post-prandial insulin response to digested and undigested liver extract was not affected by naloxone, suggesting that the foregoing effects are likely to be specific to opiate-like materials contained in foodstuff (exorphins). In view of previous findings, the present data are compatible with a role of opiate-like substances contained in ingested nutrients in the regulation of post-prandial insulin secretion.
    Type of Medium: Electronic Resource
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  • 15
    ISSN: 1432-0428
    Keywords: C-peptide ; insulin secretion ; effect of insulin ; alloxan-diabetic rats ; C-peptide effect in vivo ; somatostatin
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The effects of synthetic rat C-peptide 1 and C-peptide 2 on plasma insulin and blood glucose concentrations in the rat were studied. Infusion of rat C-peptide (500μg·h-1· kg-1) diminished glucose induced increase of plasma insulin by 56% (15.2±0.9 versus 6.6± 0.6 ng/ml, p〈0.01, mean±SEM). Somatostatin infused at a rate of 50 μg·h-1·kg-1 body weight inhibited glucose-induced insulin secretion by 33%. In the presence of a mixture of both C-peptides or somatostatin, blood glucose after intravenous glucose was higher than in the control experiments. In alloxan-diabetic rats, C-peptide (160 μg/kg) significantly increased and prolonged the hypoglycaemic effect of exogenous insulin. It is suggested that C-peptide may not be a biologically inert substance.
    Type of Medium: Electronic Resource
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  • 16
    Electronic Resource
    Electronic Resource
    Springer
    Diabetologia 19 (1980), S. 406-408 
    ISSN: 1432-0428
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 17
    Electronic Resource
    Electronic Resource
    Springer
    Diabetologia 24 (1983), S. 69-70 
    ISSN: 1432-0428
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 18
    ISSN: 1432-1106
    Keywords: Hypothalamus in vitro ; CRH ; Neurotransmitters ; Norepinephrine
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Effects of neurotransmitters on in vitro release of CRH from rat hypothalamic tissue were investigated. Three whole hypothalami or three mediobasal hypothalami from male rats, adrenalectomized 7 days before, were incubated for 10 min in a medium similar to cerebrospinal fluid at 37 ° C under 95% O2, 5% CO2. CRH activity was assayed by radioimmunological measurement of ACTH released by isolated pituitary cells from adrenalectomized rats. Norepinephrine (NE) at a concentration of 0.02×10−6 M to 2×10−6 M stimulated dose-related CRH release. At larger concentrations the response decreased again (bell-shaped dose-response relationship). The action of norepinephrine was completely blocked by coincubation with phentolamine. Similar results were obtained whether whole hypothalami or mediobasal hypothalami were incubated with norepinephrine. This suggests that the site of action of NE was within the mediobasal hypothalamus. The possibility that the observed effects were due to the CRH-like activity of vasopressin released from the hypothalamic tissue was excluded by simultaneous measurements of CRH activity and arginine-vasopressin concentrations in the medium. Dopamine at very large concentrations (17.6×10−6 M) also stimulated CRH release. Acetylcholine, serotonin, histamine and GABA did not influence the basal CRH release at any of the concentrations tested. These results suggest that in the rat, norepinephrine may have a physiological role as stimulator of CRH-release at the level of the mediobasal hypothalamus. However, in view of the conflicting results obtained with similar and other methods, no definite conclusions should yet be drawn.
    Type of Medium: Electronic Resource
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  • 19
    Electronic Resource
    Electronic Resource
    Springer
    European archives of psychiatry and clinical neuroscience 191 (1954), S. 493-507 
    ISSN: 1433-8491
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Zusammenfassung Die Beziehungen zwischen der Behandlung mit adrenocorticotropem Hormon des Hypophysenvorderlappens und dem Auftreten von Veränderungen des Hirnstrombildes (EEG) wurden bei Rheumakranken untersucht. Dabei fand sich, daß alle Arten von Veränderungen in gehäuftem Maße bei Kranken auftreten, deren Ausgangshirnstrombild stärkere Abweichungen aufweist. Im einzelnen ließ sich feststellen: 1. Bei bestimmten Personen kam es kurzfristig nach einmaliger intramuskulärer ACTH-Injektion zu Dysrhythmien, die sich bei einer Kranken bis zur Bildung von Krampfpotentialen steigerten. 2. Unter ACTH-Dauerbehandlung war im wesentlichen eine Rückbildung der von der Norm abweichenden Veränderungen des Vorbehandlungs-EEG zu beobachten. 3. Nach Absetzen des ACTH ließ sich eine über Wochen andauernde Labilität des Hirnstrombildes feststellen. Die Veränderungen des Hirnstrombildes waren weder mit dem klinischen Behandlungserfolg noch mit Stoffwechselveränderungen in Beziehung zu bringen. Für die Sofortreaktion nach einmaliger ACTH-Injektion müssen noch unbekannte, möglicherweise nervöse Faktoren verantwortlich gemacht werden. Eine Relation zwischen Psyche und EEG- Veränderungen bestand nicht.
    Type of Medium: Electronic Resource
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  • 20
    ISSN: 1591-9528
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Zusammenfassung Durch die 15 Tage andauernde, kontinuierliche parabiotische Vereinigung von an frischer, leichter Nephrotoxinnephritis erkrankten Ratten mit nierengesunden Partnern ließen sich bei den letzteren eine Dysproteinämie und Proteinurie erzeugen, die denen der nephritischen Parabionten weitgehend glichen. Histologisch waren an den Nieren der primär gesunden Tiere ähnliche Veränderungen wie bei den nephritischen Partnern, teils in schwächerem, teils im gleichen Ausmaß festzustellen. Bei den Kontrollpaaren fehlte bei quantitativ ähnlicher Dysproteinämie eine kontinuierliche Eiweißausscheidung. Histologisch fanden sich nur bei zwei Drittel der Tiere leichte und fast ausschließlich regressive Veränderungen an den Glomerula bei geringen degenerativen Tubulusschädigungen. Bei dem restlichen Drittel waren keine pathologischanatomischen Veränderungen zu beobachten. Für die Entstehung der qualitativ und quantitativ stärkeren funktionellen und morphologischen Veränderungen der primär nierengesunden Parabionten der Nephritisserie werden zwei Möglichkeiten zur Diskussion gestellt.
    Type of Medium: Electronic Resource
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