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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Zeitschrift für Rheumatologie 57 (1998), S. S72 
    ISSN: 0340-1855
    Keywords: Key words Fibromyalgia ; growth hormone ; IGF-1 ; somatostatin ; GH deficiency ; GH treatment ; Schlüsselwörter Fibromyalgie ; Wachstumshormone ; IGF-1-Somatostatin ; GH-Mangel ; GH-Behandlung
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Zusammenfassung Eine reduzierte Produktion von Wachtumshormonen (GH) wird bei 30% der Fibromyalgie-Patienten beobachtet. Die Behandlung dieser Fibromyalgie-Patienten mit rekombiniertem Wachstumshormon verbessert verschiedene klinische Symptome einschließlich der Zahl der Hauptschmerzpunkte. Die reduzierte GH-Sekretion dürfte durch einen erhöhten Tonus der Somatostatin-Freisetzung im Hypothalamus bedingt sein. Es wird die Hypothese vorgestellt, daß diese gestörte GH-Sekretion verursacht wird durch intermittierende Phasen erhöhter Cortisolspiegel, die wiederum die Dichte der β-adrenergen Rezeptoren im Hypothalamus erhöhen. Die daraus resultierende Erhöhung des β-adrenerrgen Tonus stimuliert die Freisetzung von Somatostatin mit der Folge der reduzierten GH-Sekretion.
    Notes: Summary Growth hormone (GH) deficiency occurs in about 30% of fibromyalgia patients. Treatment of GH deficient fibromyalgia patients with recombinant growth hormone improves several clinical features, including the tender point count. Defective GH secretion in these patients appears to be due to increased somatostatin tone in the hypothalamus. An hypothesis is presented which relates dysfunctional GH secretion to the effects of intermittent hypercortisolemia on upregulating the density of β-adrenergic receptors in the hypothalamus. The resulting augmentation of β-adrenergic tone stimulates the release of somatostatin, thus, impairing GH secretion.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-041X
    Keywords: Key words Tribolium castaneum ; TGF-β superfamily ; Decapentaplegic ; Dorsal/ventral axis ; Appendage development
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract  We are characterizing members of the Transforming Growth Factor-β (TGF-β) superfamily in the red flour beetle, Tribolium castaneum, in order to examine the evolutionary conservation of the structure and function of TGF-β-like genes during insect development. A decapentaplegic-like gene of the TGF-β superfamily was isolated in Tribolium (Tc dpp) that is similar in sequence, organization, and expression to the Drosophila melanogaster dpp gene (Dm dpp). Conserved features include a high degree of sequence similarity in both the pro-domain and mature domains of the encoded polypeptide. In addition, the position of an intron within the protein-coding region is conserved in Tc dpp, Dm dpp, and two bone morphogenetic protein genes of the TGF-β superfamily in humans, BMP2 and BMP4. Consensus binding sites for the dorsal transcription factor are found within this intron in Tc dpp similar to the intronic location of several dorsal binding sites in Dm dpp. During embryogenesis, Tc dpp is expressed in an anterior cap of serosa cells at the blastoderm stage, in the dorsal ectoderm at the lateral edges of the developing and extended germ band, and in the distal tips of developing embryonic appendages. Several aspects of embryonic expression, similar in both flies and beetles, suggest conserved roles for dpp in cellular communication during the development of these distantly related insects.
    Type of Medium: Electronic Resource
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