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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Inorganic chemistry 4 (1965), S. 1230-1232 
    ISSN: 1520-510X
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-0428
    Keywords: Pancreatic islets ; insulin secretion ; insulin content ; glucagon secretion ; glucagon content ; wistar rats ; sand rats ; glucose ; arginine
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Isolated pancreatic islets of normoglycemic sand rats do not respond to 2.5 mM glucose with an enhanced glucagon secretion, which could be observed in normal Wistar rats. Arginine stimulates glucagon release in the presence of 2.5 mM glucose in Wistar rats as well as in sand rats. The secretion pattern is not caused by insulin deficiency since sand rat islets are characterized by an increased insulin secretion rate in vitro. This paradoxical glucagon secretion is not caused by a changed glucagon content but might be related to this species which is able to develop a diabetic syndrome spontaneously.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Cellular and molecular life sciences 43 (1987), S. 1021-1022 
    ISSN: 1420-9071
    Keywords: Atrial natriuretic factor ; hemorrhage ; tachycardia
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Atrial natriuretic factor (ANF) is released in response to many stimuli which increase right atrial pressure. Following hemorrhage pigs lowered their atrial pressures, developed a tachycardia and increased ANF levels. Electrical pacing increased heart rate and ANF levels. There is a stimulus to ANF release other than atrial stretch, probably heart rate.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1432-0428
    Keywords: Keywords Type I (insulin-dependent) diabetes ; prediction ; screening approach ; schoolchildren ; normal population ; autoantibodies ; GADA ; IA2A ; IAA ; ICA.
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Aims/hypothesis. The Karlsburg Type I (insulin-dependent) diabetes risk study on schoolchildren aims to evaluate the predictive diagnostic value of diabetes-associated autoantibodies in the general population. Methods. We took capillary serum from 9419 schoolchildren, aged 6–17 years, for testing of autoantibodies (AAbs) to glutamic acid decarboxylase (GADA), protein tyrosine phosphatase (IA2A) and insulin (IAA) by 125I-antigen binding. We also tested for autoantibodies to cytoplasmic islet cell antigens (ICA) immunohistochemically. Results. By testing of 9419 sera for the four AAbs at cut-off at or greater than the 98th centile for the radioassayed AAbs and at or greater than 10 Juvenile Diabetes Foundation (JDF) units for ICA, 8.1 % of schoolchildren had at least one AAb. We found that 3.04, 2.97, 2.35, and 0.86 % had IAA, GADA, IA2A or ICA, respectively. 7.3 % had only one AAb and 0.8 % (75) had two or more AAbs, reflecting a risk to develop diabetes. Thus, by primary screening by combined testing of GADA and IA2A, 98.7 % (74/75) would be identified. At high AAb levels, cut-off at or greater than the 99.8th centile and at or greater than 40 JDF units for ICA, 0.23 % (22/9419) of schoolchildren, similar to the disease prevalence of 0.3 %, had two or more AAbs. Ten of 17 children tested had reduced (p 〈 0.001) first-phase insulin secretion by intravenous glucose tolerance test. Six of 22 subjects developed Type I diabetes within a follow-up of 19 ± 10 months. Conclusion/interpretation. For children older than 5 years the combined anti-GAD/IA2 test with cut-off at or greater than the 98th centile should be used for primary screening followed by testing for IAA and ICA. Subjects at risk for diabetes have two or more AAbs at or greater than the 98th centile. Subjects at risk for rapid progression to Type I diabetes have two or more AAbs at or greater than the 99.8th centile. [Diabetologia (1999) 42: 661–670]
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1432-0428
    Keywords: Isolated islets of Langerhans ; insulin secretion ; feed-back mechanism ; isolated insulin antibodies
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Mouse islets of Langerhans, isolated by microdissection after treatment with collagenase, were incubated either with pure insulin antibodies (IAB), which were prepared by immune precipitation, or with exogenous insulin. Insulin release was enhanced with increased concentrations of IAB and was inhibited by exogenous insulin. The results suggest that it was not the insulin per se, but probably its biological effect on the β-cells that influenced insulin secretion.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1432-0428
    Keywords: Monoclonal islet cell surface antibodies (mcICSA) ; anti-islet cell toxicity ; application in vivo ; pancreatic insulin content ; rat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Two monoclonal Beta-cell surface antibodies M10H6 und K14D10 were obtained by fusion of spleen cells of Balb/c mice with the myeloma cell line P30. The monoclonal antibody M10H6 was induced by immunization with rat insulinoma cells finally boostered with disintegrated rat islets, whereas the K14D10 was generated after immunization with porcine proinsulin. Both monoclonals belong to the IgG2A isotype and were screened with insulin-producing rat insulinoma cells by an indirect immunofluorescence test as well as by a cellular enzyme linked immunosorbent assay. In addition to the cell surface binding on living Beta cells the monoclonals react with islets on cryostat sections of rat pancreas. The anti-islet cytotoxic potential of these monoclonals was measured by 51Chromium-release in the presence of complement or Fc-receptor bearing leucocytes using 51Chromium-labelled rat islet cells as target. Both antibody secreting hybridomas were propagated in syngeneic mice resulting in high levels of islet cell surface antibodies in ascites and sera from the recipient. High anti-islet cytotoxicity was mediated by ascites fluid, but no mouse developed hyperglycaemia. Furthermore, the repeated injections of the monoclonals into rats did not exert a diabetogenic action and failed to reduce the pancreatic insulin content although the attraction of the K14D10 to the pancreatic islets in vivo could be demonstrated. We conclude that islet cell surface antibody-mediated Beta-cell lysis in vitro may not be relevant to Beta-cell destruction in vivo.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1432-0428
    Keywords: Insulin antibodies ; immunotolerance ; mode of insulin application
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Résumé 1. Après une adaption lentement progressive à l'insuline (insuline normale du commerce, mélange d'insulines de boeuf et de porc), deux chiens n'ont montré aucun anticorps circulant contre l'insuline, malgré l'application quotidienne sous-cutanée de 4 IU/kg durant plus de deux ans. — 2. La non-apparition d'anticorps circulants contre l'insuline a été confirmée par plusieurs expériencesin vitro etin vivo, en particulier par autoradiographie — immunoélectrophorèse et détermination d'IBC aussi bien avant qu'après avoir retiré l'insuline du sérum. — 3. L'activité biologique de l'insuline de boeuf non marquée, après l'injection intra-veineuse, n'a pas diminué chez les chiens adaptés à l'insuline.
    Abstract: Zusammenfassung 1. Nach einer langsam ansteigenden Anpassung an Insulin (kommerzielles Alt-Insulin, eine Mischung von Rinder- und Schweineinsulin) zeigten 2 Hunde keine zirkulierenden Insulinantikörper, obwohl 4 IE/kg Körpergewicht über zwei Jahre täglich subcutan injiziert wurden. — 2. Das Fehlen von zirkulierenden Insulinantikörpern wurde durch verschiedene Experimentein vitro undin vivo, insbesondere durch Autoradiographie — Immunelektrophorese und Bestimmung der IBC vor und nach Entfernung des Insulins aus dem Serum bekräftigt. — 3. Die biologische Aktivität unmarkierten Rinderinsulins war nach i.v.-Injektion bei den adaptierten Hunden nicht vermindert.
    Notes: Summary 1. After a slowly increased adaptation to insulin (commercial normal insulin, i.e. a mixture of bovine-porcine insulin) two dogs showed no circulating insulin antibodies, despite daily subcutaneous application of 4 IU/kg body weight for more than 2 years. — 2. The non-appearance of circulating insulin antibodies was confirmed by several experimentsin vitro andin vivo especially by autoradiography — immunoelectrophoresis and determination of IBC before as well as after the removal of insulin from the serum. — 3. The biological activity of unlabelled bovine insulin after I.V. injection was not diminished in the dogs adapted to insulin.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Diabetologia 8 (1972), S. 104-110 
    ISSN: 1432-0428
    Keywords: Oral glucose tolerance test ; insulin secretion ; feed-forward ; enterohormones ; N.vagus ; reflex
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Résumé Chez des chiens-bergers éveillés et entraînés, après administration orale de glucose, la concentration d'IRI dans le sang veineux périphérique augmente déjà alors que la glycémie n'a pas encore changé. Après un ou deux pics durant les vingt premières minutes, l'IRI augmente parallèlement au glucose sanguin. Comparativement à l'injection intra-veineuse de glucose, le maximum d'IRI, après administration orale, se produit plus tôt. De plus, le quotient des surfaces d'IRI et de glycémie est élevé. Sans aucun changement du glucose sanguin, la concentration d'IRI augmente avec un ou deux pics après administration orale d'eau potable. Ces pics correspondent aux deux premiers pics après administration orale de glucose. Ces résultats sont discutés dans le sens d'une sécrétion d'insuline précédant la digestion via N.vague et via entérohormones. Il faut accorder plus d'attention à l'évolution d'IRI durant la première phase du test de tolérance au glucose par voie orale.
    Abstract: Zusammenfassung Bei wachen trainierten Schäferhunden steigt die Insulinkonzentration im peripheren Venenblut nach oraler Glucosegabe schon zu einem Zeitpunkt an, da die Glykämie noch nicht verändert ist. Nach Durchlaufen von 1 oder 2 Gipfeln in den ersten 20 min tritt der Anstieg ein, der parallel dem Blutzuckergipfel verläuft. Im Verhältnis zur intravenösen Glucosegabe liegt das erste IRI-Maximum nach oraler Verabfolgung zeitlich früher. Auch ist der Quotient aus IRIÜberschreitungsfläche und Blutzuckerüberschreitungsfläche erhöht. Ohne daß es zu einer Blutzucker Veränderung kommt, steigt auch nach oraler Gabe von Leitungswasser die IRI-Konzentration 1-oder 2gipflig an. Diese Gipfel entsprechen den beiden ersten Erhöhungen nach oraler Glucosegabe. Die beobachteten Phänomene werden im Sinne einer Vorwärtskopplung der Insulinsekretion nach Nahrungsaufnahme via N.vagus und Enterohormone diskutiert. Der Beurteilung des IRI-Verlaufs in der frühen Phase des oralen Glucosetoleranztests sollte größere Beachtung geschenkt werden.
    Notes: Summary In conscious trained dogs (Alsatians) the IRI-concentration in the peripheral venous blood after oral administration of glucose increases when the blood glucose is still unchanged. After one or two peaks during the first 20 min IRI increases parallel to the blood sugar increase. In relation to the intravenous injection of glucose the IRI maximum after oral administration occurs earlier. Furthermore the ratio of the IRI to blood sugar areas is raised. Without any blood sugar change the IRI concentration after oral application of tap water increases with one or two peaks. These peaks correspond to the first peaks after oral administration of glucose. These findings are discussed in the sense of a “feed-forward” of insulin secretion after feeding via N.vagus as well as via enterohormones. More attention should be payed to the IRI course during the early phase of the oral glucose tolerance test.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Diabetologia 8 (1972), S. 385-390 
    ISSN: 1432-0428
    Keywords: Oral glucose tolerance test ; insulin secretion ; reflex ; glucose doses ; receptor ; mucosal anaesthesia ; cyclamate
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Résumé Des expériences préalables ont montré que dans un test oral de tolérance au glucose l'insuline est mobilisée au cours de la première phase indépendamment de l'hyperglycémie qui suit. Si l'on administre différentes doses de glucose (0.5–2.0 g/kg) à des chiens éveillés et entrainés, il apparaît que cette première phase de la sécrétion d'insuline est stimulée par des mécanismes additifs indépendamment de la charge de glucose appliquée. Ces mécanismes, au moins en partie, commencent aux terminaisons nerveuses de la cavité buccale: leur paralysie par anesthésie de la muqueuse empêche la première augmentation réflexe d'IRI chez les animaux intacts de même que l'augmentation d'IRI après alimentation simulée de glucose chez des chiens ayant des fistules de l'oesophage. Le fait de pulvériser du cyclamate de sodium dans la cavité buccale ne provoque aucune augmentation d'IRI. Cela signifie que la saveur “sucrée” n'intervient pas dans le mécanisme du réflexe. Les mécanismes des réflexes conditionnés qui sont la conséquence d'un programme d'entraînement ou d'un régime alimentaire journalier étaient exclus par des expériences de contrôle.
    Abstract: Zusammenfassung Vorangegangene Experimente hatten ergeben, daß bei einem oralen Glucosetoleranztest in einer ersten Phase Insulin unabhängig von der erst darauffolgenden Hyperglykämie freigesetzt wird. Durch Gabe unterschiedlicher Glucosedosen (0.5–2.0 g/kg) an wache, trainierte Schäferhunde wird in dieser Mitteilung gezeigt, daß diese erste Phase der Insulinsekretion von der verabfolgten Glucosedosis unabhängig durch zusätzliche Mechanismen stimuliert wird. Diese Mechanismen beginnen zumindest teilweise in Nervenendigungen der Mundhöhle: ihre Betäubung durch Schleimhautanästhesie verhindert den frühzeitigen reflektorischen IRI-Anstieg bei intakten Tieren sowie den gleichen reflektorischen IRI-Anstieg nach Glucosescheinfütterung an Hunde mit Oesophagusfisteln. Einstäuben von Natrium-Zyklamat in die Mundhöhle ruft keinen IRI-Anstieg hervor. Die Geschmacksrichtung „süß” ist also nicht an den reflektorischen Mechanismen beteiligt. Bedingt-reflektorische Vorgänge als Folge des Trainingsprogramms oder der täglichen Nahrungsaufnahme wurden durch Kontrollversuche ausgeschlossen.
    Notes: Summary Previous experiments have shown that in an oral glucose tolerance test insulin is mobilized in the first phase independent of the following hyperglycemia. By giving different amounts of glucose (0.5–2.0 g/kg) in conscious trained dogs it was shown that this early phase of insulin secretion was stimulated independently of the administered glucose load by additional mechanisms. These mechanisms, at least partly, were triggered in the nerve endings of the cavity of mouth: their paralysis by mucosal anaesthesia abolished the early IRI-increase in intact animals as well as after feeding glucose to dogs bearing oesophagus fistulas. Spraying sodium cyclamate into the mouth did not produce any IRI-increase. The results indicate that the taste modality “sweet” is not involved in this reflex response. Conditioned reflexes as a consequence of the training programme or of the daily feeding regime were excluded by control experiments.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Cellular and molecular life sciences 26 (1970), S. 906-907 
    ISSN: 1420-9071
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Subcutaneous injection of exogenous insulin always results in a production of antibodies against insulin. But after a slowly increased dose of insulin (a daily end dose of 3.5–4.2 U/kg) insulin antibodies could not be found in the serum of 2 dogs. This failure of immunogenic action of insulin is discussed as an induction of immunotolerance by the modus of initial antigen application.
    Type of Medium: Electronic Resource
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