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  • 1
    In: Diabetologia, Springer Science and Business Media LLC, Vol. 8, No. 5 ( 1972-11), p. 362-370
    Type of Medium: Online Resource
    ISSN: 0012-186X , 1432-0428
    RVK:
    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 1972
    detail.hit.zdb_id: 1458993-X
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  • 2
    In: Acta Medica Scandinavica, Wiley, Vol. 189, No. 1-6 ( 1971-01-12), p. 415-422
    Abstract: Abstract. Twohundred and thirty‐one subjects with borderline glucose tolerance, detected during a diabetes survey performed in Malmöhus County 1962–1965, have been followed up for 3–5 years. In the newly discovered state selected cases were studied with determinations of seruminsulin‐like activity (SILA) in the fasting state and during oral glucose tolerance tests (OGTT), and with determinations of plasma free fatty acids (FFA), fasting and during a short exercise test. It was found that the SILA values of the borderline cases did not differ from those of normal subjects. In the fasting state the plasma FFA level of the borderline cases was somewhat elevated, but during the exercise test no difference was noticed in comparison with normal subjects. Intravenous glucose tolerance tests (IGTT) were performed in the subjects in groups II‐IV and in a control group. The K‐values in the borderline groups were significantly lower than that of the control group. The borderline cases were separated into four groups: group I was given no instructions at all, group II dietary instructions, group III diet and tolbutamide 1.5 g daily, and group IV diet and placebo tablets. In none of the groups did any individual pass into a state of clinical overt diabetes during the observation period, and no deterioration of the carbohydrate tolerance was observed as judged by repeated OGTTs. It is concluded that the progress of glucose intolerance, if any, is slow and that further observation of the borderline cases is necessary to reveal whether such subjects are candidates for clinical diabetes.
    Type of Medium: Online Resource
    ISSN: 0001-6101
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 1971
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  • 3
    In: Cell Metabolism, Elsevier BV, Vol. 10, No. 4 ( 2009-10), p. 309-315
    Type of Medium: Online Resource
    ISSN: 1550-4131
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2009
    detail.hit.zdb_id: 2174469-5
    SSG: 12
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  • 4
    Online Resource
    Online Resource
    Oxford University Press (OUP) ; 1967
    In:  Acta Endocrinologica Vol. 56, No. 4 ( 1967-12), p. 713-725
    In: Acta Endocrinologica, Oxford University Press (OUP), Vol. 56, No. 4 ( 1967-12), p. 713-725
    Abstract: The hypoglycaemic effect of synthetic tetraicosapeptide corticotrophin was investigated in NMRI mice in order to determine its physiological significance as well as its mechanism of action. It was found that in normal non-fasting mice corticotrophin produced a maximal hypoglycaemic response at a dose level of about 5 μg per 20 g mouse (1250 milliunits per 20 g mouse). The ED 50 of the hypoglycaemic effect was about 1000 times larger than the ED 50 for adrenal cortical stimulation. Immunoassayable insulin was markedly increased 15 minutes following 5 μg of corticotrophin, whereas following a maximal steroidogenic dose (1.6 nanogram) or following ether stress the plasma insulin levels were normal. In adrenalectomized mice the administration of 5 μg of corticotrophin had practically no effect on the blood glucose level, whereas pretreatment with a glucocorticosteroid in adrenalectomized mice markedly restored the hypoglycaemic response. Acutely hypophysectomized mice showed a hypoglycaemic response to corticotrophin indistinguishable from that found in normal mice, whereas animals hypophysectomized 3–7 days before corticotrophin injection showed a smaller response. Corticotrophin in a dose of 5 μg per 20 g mouse had no hypoglycaemic effect in mice with manifest alloxan diabetes. Corticotrophin injected 5 minutes following a diabetogenic dose of alloxan hardly had any measurable effect on the acute initial alloxan hyperglycaemia, whereas the latter was greatly reduced when corticotrophin was given 5 minutes before alloxan administration. Pretreatment with corticotrophin did not change the frequency or intensity of the ensuing diabetic condition in mice. It is concluded that the corticotrophin induced hypoglycaemia is dependent on 1) the presence of normally functioning pancreatic beta-cells; and 2) the presence of glucocorticosteroids. It is doubtful whether the observed hypoglycaemia has any physiological significance.
    Type of Medium: Online Resource
    ISSN: 0804-4643 , 1479-683X
    RVK:
    Language: Unknown
    Publisher: Oxford University Press (OUP)
    Publication Date: 1967
    detail.hit.zdb_id: 1485160-X
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  • 5
    Online Resource
    Online Resource
    Oxford University Press (OUP) ; 1979
    In:  Acta Endocrinologica Vol. 92, No. 1 ( 1979-09), p. 166-173
    In: Acta Endocrinologica, Oxford University Press (OUP), Vol. 92, No. 1 ( 1979-09), p. 166-173
    Abstract: It has recently been suggested from experiments in dogs that somatostatin suppresses insulin release via a stimulation of the inhibitory α-adrenoceptors of the pancreatic B-cell. The effect of somatostatin on insulin secretion during α-adrenergic blockade with phentolamine was therefore studied in three different species; the rat, the cat and the mouse. It was found that somatostatin significantly depressed insulin release during α-adrenoceptor blockade in all three species. In the rat, infusion of somatostatin at a dose of 0.3 μg/kg/min decreased basal plasma insulin concentration by 92 %. In the presence of phentolamine, the same dose of somatostatin lowered plasma insulin by 85 %. In the cat, a similar infusion of somatostatin lowered basal plasma insulin concentration by 87 %, but its depressive effect during α-adrenergic blockade was comparatively less pronounced (68 %) than in the rat. In the mouse, a single iv injection of somatostatin induced a short-lasting depression of plasma insulin concentration during α-adrenergic blockade. From these results it seems unlikely that somatostatin should inhibit insulin release simply by stimulation of α-adrenoceptors on the B-cell. It cannot be ruled out, however, that a more complex interaction exists between somatostatin and the sympatho-adrenal system with regard to the control of insulin secretion.
    Type of Medium: Online Resource
    ISSN: 0804-4643 , 1479-683X
    RVK:
    Language: Unknown
    Publisher: Oxford University Press (OUP)
    Publication Date: 1979
    detail.hit.zdb_id: 1485160-X
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  • 6
    Online Resource
    Online Resource
    Oxford University Press (OUP) ; 1981
    In:  Acta Endocrinologica Vol. 97, No. 4 ( 1981-08), p. 508-513
    In: Acta Endocrinologica, Oxford University Press (OUP), Vol. 97, No. 4 ( 1981-08), p. 508-513
    Abstract: The influence of long-term changes in thyroid state on insulin secretion was investigated in vivo in mice. Hyperthyroidism was induced by daily injections of i .-triiodothyronine and hypothyroidism by a single injection of 131 I. Four different insulin secretagogues were used to characterize the insulin secretory response, i.e. glucose, the β 2 -adrenoceptor agonist terbutaline, the cholinergic agonist carbachol and the synthetic C-terminal octapeptide of cholecystokinin, CCK-8. In the hyperthyroid mice the plasma glucose level was moderately decreased. Despite this lower glucose level the insulin response to terbutaline and glucose were potentiated by about 200%. Insulin response to CCK-8 and carbachol was less enhanced, by about 100 and 50%, respectively. Liver and muscle glycogen levels were markedly reduced. The hypothyroid animals showed reduced insulin responses to all secretagogues; after terbutaline by 100%, after carbachol by 70%, after glucose and CCK-8 by 50%. Plasma glucose and muscle glycogen levels were normal, whereas liver glycogen levels were moderately enchanced. Insulin release induced by β-adrenoceptor stimulation was most markedly affected by the thyroid state, which thus may be of importance for the balance between the β- and α-adrenoceptors of the insulin cell. Since thyroid activity influenced the insulin response to all secretagogues it cannot be excluded that the thyroid state also exerts effects not related to the adrenoceptors.
    Type of Medium: Online Resource
    ISSN: 0804-4643 , 1479-683X
    RVK:
    Language: Unknown
    Publisher: Oxford University Press (OUP)
    Publication Date: 1981
    detail.hit.zdb_id: 1485160-X
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  • 7
    In: Journal of Endocrinology, Bioscientifica, Vol. 190, No. 3 ( 2006-09), p. 681-693
    Abstract: We have studied the influence of nitric oxide (NO) and carbon monoxide (CO), putative messenger molecules in the brain as well as in the islets of Langerhans, on glucose-stimulated insulin secretion and on the activities of the acid α-glucoside hydrolases, enzymes which we previously have shown to be implicated in the insulin release process. We have shown here that exogenous NO gas inhibits, while CO gas amplifies glucose-stimulated insulin secretion in intact mouse islets concomitant with a marked inhibition (NO) and a marked activation (CO) of the activities of the lysosomal/vacuolar enzymes acid glucan-1,4-α-glucosidase and acid α-glucosidase (acid α-glucoside hydrolases). Furthermore, CO dose-dependently potentiated glucose-stimulated insulin secretion in the range 0.1–1000 μM. In intact islets, the heme oxygenase substrate hemin markedly amplified glucose-stimulated insulin release, an effect which was accompanied by an increased activity of the acid α-glucoside hydrolases. These effects were partially suppressed by the guanylate cyclase inhibitor 1H-[1,2,4]oxadiazolo-[4,3-a] quinoxalin-1-one. Hemin also inhibited inducible NO synthase (iNOS)-derived NO production probably through a direct effect of CO on the NOS enzyme. Further, exogenous CO raised the content of both cGMP and cAMP in parallel with a marked amplification of glucose-stimulated insulin release, while exogenous NO suppressed insulin release and cAMP, leaving cGMP unaffected. Emiglitate, a selective inhibitor of α-glucoside hydrolase activities, was able to markedly inhibit the stimulatory effect of exogenous CO on both glucose-stimulated insulin secretion and the activityof acid glucan-1,4-α-glucosidase and acid α-glucosidase, while no appreciable effect on the activities of other lysosomal enzyme activities measured was found. We propose that CO and NO, both produced in significant quantities in the islets of Langerhans, have interacting regulatory roles on glucose-stimulated insulin secretion. This regulation is, at least in part, transduced through the activity of cGMP and the lysosomal/vacuolar system and the associated acid α-glucoside hydrolases, but probably also through a direct effect on the cAMP system.
    Type of Medium: Online Resource
    ISSN: 0022-0795 , 1479-6805
    Language: Unknown
    Publisher: Bioscientifica
    Publication Date: 2006
    detail.hit.zdb_id: 1474892-7
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  • 8
    In: PLoS ONE, Public Library of Science (PLoS), Vol. 3, No. 5 ( 2008-5-20)
    Type of Medium: Online Resource
    ISSN: 1932-6203
    Language: English
    Publisher: Public Library of Science (PLoS)
    Publication Date: 2008
    detail.hit.zdb_id: 2267670-3
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  • 9
    Online Resource
    Online Resource
    American Physiological Society ; 1998
    In:  American Journal of Physiology-Endocrinology and Metabolism Vol. 275, No. 3 ( 1998-09-01), p. E500-E506
    In: American Journal of Physiology-Endocrinology and Metabolism, American Physiological Society, Vol. 275, No. 3 ( 1998-09-01), p. E500-E506
    Abstract: Nitric oxide (NO) produced by islet constitutive NO synthase (cNOS) is a putative modulator of islet hormone secretion. We show here for the first time that the release of insulin induced byl-arginine orl-homoarginine is inhibited and that of glucagon stimulated in parallel with the rate of islet NO production. It was found thatl-homoarginine was ≈25–30% less potent thanl-arginine as an insulin secretagogue but equally potent as a glucagon secretagogue. Biochemical determination of islet cNOS activity revealed that the NO production with l-homoarginine as substrate was only ≈40% of that ofl-arginine. Selective inhibition of islet cNOS potentiated insulin release during amino acid stimulation. Moreover, inhibition of cNOS suppressed glucagon release, more so with l-arginine than with l-homoarginine as secretagogue, reflecting the relative rates of their NO production. In K + -depolarized islets, inhibition of cNOS enhanced the insulin response tol-arginine by 50% and that tol-homoarginine by 23%, largely corresponding to their relative NO production. The intracellular NO donor hydroxylamine dose dependently inhibited insulin but increased glucagon secretion in K + -depolarized and amino acid-stimulated islets. We conclude that both amino acids have a dual action on insulin release, since their stimulatory effects are reduced in parallel with the rates of their NO production. Furthermore, the greater NO production induced byl-arginine relative tol-homoarginine corresponds to NO-mediated increases in glucagon release. These NO effects are mainly exerted independently of membrane depolarization events.
    Type of Medium: Online Resource
    ISSN: 0193-1849 , 1522-1555
    Language: English
    Publisher: American Physiological Society
    Publication Date: 1998
    detail.hit.zdb_id: 1477331-4
    SSG: 12
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  • 10
    Online Resource
    Online Resource
    Oxford University Press (OUP) ; 1966
    In:  Acta Endocrinologica Vol. 52, No. 3 ( 1966-07), p. 357-367
    In: Acta Endocrinologica, Oxford University Press (OUP), Vol. 52, No. 3 ( 1966-07), p. 357-367
    Abstract: Multiple serial blood glucose level determinations in individual mice were performed on small blood samples (10–25 μl) using the orbital bleeding technique. Glucose was determined specifically by a known enzymatic reaction. Blood glucose determined in this way was found a parameter of high reproducibility and precision, the latter being shown by the finding that differences between individual animals were highly significant in practically all the experiments. The standard deviation of the single measurement in normal mice was ± 8.2 mg/100 ml as determined from 600 samples, which indicated that the technique allows of the detection of blood sugar level changes of about 15 mg/100 ml or more with very high significance, in a group of 5 mice. In the sampling procedure as such, intravenous or subcutaneous saline injections did not necessarily have any effect on the blood glucose level, but interpretation of slight blood sugar changes under experimental conditions should always be based on a comparison with control groups, since the latter may sometimes show a slight but significant change. In normal non-fasting mice (NMRI strain) significant differences in homoeostatic blood glucose level adjustments were demonstrated. In acutely adrenalectomized mice blood glucose levels were lower and more variable than in normals. Alloxan injection (70 mg/kg) was followed in individual mice by a triphasic blood sugar response, as is known from other species.
    Type of Medium: Online Resource
    ISSN: 0804-4643 , 1479-683X
    RVK:
    Language: Unknown
    Publisher: Oxford University Press (OUP)
    Publication Date: 1966
    detail.hit.zdb_id: 1485160-X
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