1990
DOI: 10.1016/0024-3205(90)90563-7
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Oral activity of the growth hormone releasing peptide His-D-Trp-Ala-Trp-D-Phe-Lys-NH2 in rats, dogs and monkeys

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Cited by 87 publications
(35 citation statements)
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“…These observations are compatible with findings in humans, showing that not only the GH-releasing effect of ghrelin (Broglio et al, 2003) but also that of GHRH and peptidyl or non-peptidyl synthetic GHSs undergoes an age-related decrease (Aloi et al, 1994;Bowers et al, 1992;Broglio et al, 2003;Chapman et al, 1996;Muccioli et al, 2002). In old rats, the GH response to synthetic GHSs is impaired as well (Ceda et al, 1986;Walker et al, 1990). Also in old dogs, the GH responsiveness to the synthetic GHS hexarelin has been reported to be low (Cella et al, 1995).…”
Section: Discussionsupporting
confidence: 85%
See 1 more Smart Citation
“…These observations are compatible with findings in humans, showing that not only the GH-releasing effect of ghrelin (Broglio et al, 2003) but also that of GHRH and peptidyl or non-peptidyl synthetic GHSs undergoes an age-related decrease (Aloi et al, 1994;Bowers et al, 1992;Broglio et al, 2003;Chapman et al, 1996;Muccioli et al, 2002). In old rats, the GH response to synthetic GHSs is impaired as well (Ceda et al, 1986;Walker et al, 1990). Also in old dogs, the GH responsiveness to the synthetic GHS hexarelin has been reported to be low (Cella et al, 1995).…”
Section: Discussionsupporting
confidence: 85%
“…GHRH, despite the availability of a remarkable GHreleasable pool (Giustina and Veldhuis, 1998;Ghigo et al, 1999;Muccioli et al, 2002). These observations support the idea that the somatopause is driven primarily by the hypothalamus and that the pituitary somatotropes retain their capacity to synthesise and secrete adequate levels of GH (Cella et al, 1993;Corpas et al, 1992;Franchimont et al, 1989;Muccioli et al, 2002;Muller et al, 1999;Walker et al, 1990).…”
Section: Discussionmentioning
confidence: 84%
“…The activity of GHRP in releasing GH was observed when administered directly into the gastrointestinal tract in rats, dogs and monkeys [27]. In man, GHRP infusion resulted in a selective and dose-dependent increase in serum GH concentrations [28].…”
Section: Discussionmentioning
confidence: 97%
“…The [20]; however, no correction was made for the molar ratio. In monkeys, orally administered GHRP was reported to be 5-20 times more effective than in rats or dogs [43].…”
Section: Introductionmentioning
confidence: 99%
“…GHRP also stimulates release of GH in rat, primate, chick, porcine, ovine and bovine species [8,10,19,20,31]. Furthermore the peptide is efficient if orally administered in rats, dogs and monkeys [43], and in man [14,27]; however, its effect is about 300-fold less potent than when administered i.v.…”
Section: Introductionmentioning
confidence: 99%