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  • 1
    Online Resource
    Online Resource
    Oxford University Press (OUP) ; 1980
    In:  Acta Endocrinologica Vol. 93, No. 3 ( 1980-03), p. 315-321
    In: Acta Endocrinologica, Oxford University Press (OUP), Vol. 93, No. 3 ( 1980-03), p. 315-321
    Abstract: In order to compare the acute effects of three methods of treatment in hyperthyroid patients with diffuse goitre, values of thyroxine (T 4 ), triiodothyronine (T 3 ) in serum, T 3 -resin uptake (T 3 -U), free thyroxine index (FT 4 I) and free triiodothyronine index (FT 3 I) were employed as thyroid function parameters. In iodide (I − ) group given iodine (3 or 6 mg/day) as iodinated lecithine once daily, the parameters were reduced acutely within one week after the start of treatment, reaching a plateau during the next week. In contrast to the changes in I − group, the thyroid function was decreased gradually and consistently for two weeks in the propylthiouracil (PTU 300 mg/day) group. In PTU + I − (300 mg/PTU plus 3 or 6 mg/iodide/day) group, the parameters were reduced acutely and progressively for two weeks. These results indicate that PTU +I − therapy is much more effective than PTU or I − alone in early phase treatment of hyperthyroidism. Another new finding was that the thyroid function increased again during the later addition of PTU (300 mg/day) in the patients treated with I − (3 or 6 mg/day) for one or two weeks. The well-known escape phenomenon from iodide inhibition took place counteracted the effect of PTU. Since blocking of thyroidal secretion by I − is only transient while synthesis of T 3 and T 4 continues, leading to greater amount of hormone stored in the gland, the treatment of hyperthyroidism with I − alone is a risky procedure.
    Type of Medium: Online Resource
    ISSN: 0804-4643 , 1479-683X
    RVK:
    Language: Unknown
    Publisher: Oxford University Press (OUP)
    Publication Date: 1980
    detail.hit.zdb_id: 1485160-X
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  • 2
    Online Resource
    Online Resource
    Oxford University Press (OUP) ; 1987
    In:  Acta Endocrinologica Vol. 114, No. 3 ( 1987-03), p. 396-401
    In: Acta Endocrinologica, Oxford University Press (OUP), Vol. 114, No. 3 ( 1987-03), p. 396-401
    Abstract: Abstract. The nature of epidermal growth factor (EGF) receptors in normal and pathological thyroid membranes was studied on a crude membrane fraction (10 000 × g pellet) of tissue homogenate. Optimal binding of 125 I-EGF to human thyroid membranes was obtained at 25°C with 1-h incubation at pH 7.4. The study revealed the presence of both high and low affinity receptors in normal and pathological thyroid membranes. The association constants of high affinity receptor (3.2 × 10 −9 mol/l) and of low affinity receptor (1.8 × 10 −8 mol/l) observed in normal thyroid membranes were similar to those of thyroid membranes from neoplastic as well as thyrotoxic thyroid tissues. [ 3 H]thymidine incorporation into DNA of cultured human thyroid cells was stimulated by EGF in a dose-dependent manner. A half-maximal stimulation was found around 1 × 10 −10 mol/l. These results suggest that EGF may have a possible role in the regulation of thyroid growth and function in physiological and pathological situations.
    Type of Medium: Online Resource
    ISSN: 0804-4643 , 1479-683X
    RVK:
    Language: Unknown
    Publisher: Oxford University Press (OUP)
    Publication Date: 1987
    detail.hit.zdb_id: 1485160-X
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  • 3
    Online Resource
    Online Resource
    Oxford University Press (OUP) ; 1985
    In:  Acta Endocrinologica Vol. 108, No. 2 ( 1985-02), p. 200-205
    In: Acta Endocrinologica, Oxford University Press (OUP), Vol. 108, No. 2 ( 1985-02), p. 200-205
    Abstract: Abstract. Forskolin stimulates adenylate cyclase in human thyroid membranes approximately 7-fold with halfmaximal stimulation occurring at 5–10 μ m . Guanine nucleotides are not required for stimulation of the enzyme by forskolin. Forskolin-stimulation is additive or greater than additive with that of TSH or Gpp(NH)p-(above 1 μ m ). Different from TSH- or Gpp(NH)p-stimulation of adenylate cyclase, uncoupling of the guanine nucleotide-binding regulatory component by increasing concentrations of MnCl 2 did not result in uncoupling of forskolin stimulation. The finding indicates that forskolin may mainly act on the catalytic component of adenylate cyclase. From the present study, it is suggested that the diterpene forskolin stimulates adenylate cyclase in human thyroid membranes by a novel mechanism that differs from TSH- or Gpp(NH)p-stimulation, and that the diterpene may be a useful tool to investigate the metabolism of thyroid and its regulation in normal and pathological situations.
    Type of Medium: Online Resource
    ISSN: 0804-4643 , 1479-683X
    RVK:
    Language: Unknown
    Publisher: Oxford University Press (OUP)
    Publication Date: 1985
    detail.hit.zdb_id: 1485160-X
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  • 4
    Online Resource
    Online Resource
    Oxford University Press (OUP) ; 1980
    In:  Acta Endocrinologica Vol. 93, No. 3 ( 1980-03), p. 283-286
    In: Acta Endocrinologica, Oxford University Press (OUP), Vol. 93, No. 3 ( 1980-03), p. 283-286
    Abstract: The influence of glycine, the simplest amino acid, on pituitary function has been investigated in the present study. Different doses (4, 8 or 12 g) of glycine were intravenously infused over 15 or 30 min in normal subjects. Serum levels of GH (growth hormone) and Prl (prolactin) were measured before and after the infusion, and also blood sugar levels were determined. The dose of 4 or 8 g glycine induced a significant increase in serum GH ( P 〈 0.05 or P 〈 0.001, respectively); however, a more pronounced and significant increase in serum GH levels was observed after infusion at a dose of 12 g glycine ( P 〈 0.001). It was clearly observed that the dose-dependent GH release to intravenous glycine occurred in normal subjects. On the contrary, serum Prl level was not changed significantly, and blood sugar level was transiently, but significantly ( P 〈 0.05), increased after the infusion of 12 g glycine. The present data suggest that glycine might play an important role in the control of hypothalamic-pituitary function.
    Type of Medium: Online Resource
    ISSN: 0804-4643 , 1479-683X
    RVK:
    Language: Unknown
    Publisher: Oxford University Press (OUP)
    Publication Date: 1980
    detail.hit.zdb_id: 1485160-X
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  • 5
    Online Resource
    Online Resource
    The Electrochemical Society ; 1994
    In:  Journal of The Electrochemical Society Vol. 141, No. 8 ( 1994-08-01), p. 2265-2265
    In: Journal of The Electrochemical Society, The Electrochemical Society, Vol. 141, No. 8 ( 1994-08-01), p. 2265-2265
    Type of Medium: Online Resource
    ISSN: 0013-4651 , 1945-7111
    RVK:
    Language: Unknown
    Publisher: The Electrochemical Society
    Publication Date: 1994
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  • 6
    Online Resource
    Online Resource
    The Electrochemical Society ; 1994
    In:  Journal of The Electrochemical Society Vol. 141, No. 5 ( 1994-05-01), p. 1334-1338
    In: Journal of The Electrochemical Society, The Electrochemical Society, Vol. 141, No. 5 ( 1994-05-01), p. 1334-1338
    Type of Medium: Online Resource
    ISSN: 0013-4651 , 1945-7111
    RVK:
    Language: Unknown
    Publisher: The Electrochemical Society
    Publication Date: 1994
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  • 7
    Online Resource
    Online Resource
    Walter de Gruyter GmbH ; 1998
    In:  Pteridines Vol. 9, No. 1 ( 1998-02), p. 8-12
    In: Pteridines, Walter de Gruyter GmbH, Vol. 9, No. 1 ( 1998-02), p. 8-12
    Abstract: Cardiac myocytes are known to express the high-capacity inducible isoform of nitric oxide (NO) synthase (iNOS). Since tetrahydrobiopterin (BH 4 ) is an essential cofactor for NO formation, we investigated whether BH 4 synthesis is required for cytokine-induced NO production in cultutred rat cardiac myocytes. The total biopterin content of untreated cardiac myocytes was below our limit of detection. However, treatment with inter-leukin-1α. and interferon-γ (IL-1/IFN) caused a significant rise in biopterin levels and induced NO synthesis. iNOS mRNA and GTP cyclohydrolase I (GTPCH) mRNA were induced by IL-1/IFN in parallel. 2,4-Diamino-6-hydroxypyridine (DAHP), a selective inhibitor of GTPCH, inhibited both the increase in cellular levels of BH 4 as well as the concomitant formation of NO caused by IL-1/IFN. This inhibition by DAHP was reversed by coaddition of sepiapterin which is a substrate for BH 4 synthesis. Thus BH 4 synthesis is an absolute requirement for induction of NO synthesis by cytokines in cardiac myocytes.
    Type of Medium: Online Resource
    ISSN: 2195-4720 , 0933-4807
    Language: Unknown
    Publisher: Walter de Gruyter GmbH
    Publication Date: 1998
    detail.hit.zdb_id: 2279565-0
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