4.5 Article

Differential Effects of Insufflated, Subcutaneous, and Intravenous Growth Hormone on Bone Growth, Cognitive Function, and NMDA Receptor Subunit Expression

Journal

ENDOCRINOLOGY
Volume 151, Issue 9, Pages 4418-4427

Publisher

OXFORD UNIV PRESS INC
DOI: 10.1210/en.2010-0152

Keywords

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Funding

  1. Ministry for Health, Welfare, and Family Affairs, Republic of Korea [A080588]
  2. Samsung Biomedical Research Institute [SBRI C-A6-227-3, C-A9-240-2]
  3. Cystic Fibrosis Foundation
  4. American Association of Pharmaceutical

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The objective of this study was to characterize the effect of inhalable growth hormone (GH) delivered by an insufflator to the lungs of hypophysectomized Sprague Dawley rats. In the first cohort, the safety and efficacy of the insufflated GH were evaluated. Three experimental groups (n = 7 per group) were treated with GH for 15 d: One group received sc injection of GH daily at 200 mu g/kg (SC200). Two other groups received GH by insufflation daily: 200 mu g/kg (INS 200) and 600 mu g/kg (INS 600). In the second set of experiments, GH was administered in three routes[SC200, INS200, intravenous (IV200)] (n = 10) for 5 d, and escape latency and N-methyl D-aspartate (NMDA) receptor expression were evaluated. In the first cohort, INS200 showed similar bioactivity as SC200 in growth promotion, tibial growth, as well as escape latency on the 12th day of treatment. Insufflated GH was well tolerated without significant inflammatory responses. In the second cohort, expression of the NMDA receptor 1 and 2B in hippocampus measured after 3 or 6 d of daily treatments were significantly higher in INS200 as compared to IV200, consistent with the improvement of the escape latency. In summary, the inhalable form of GH delivered by intratracheal insufflation was safe, and its bioactivity was comparable to sc injection both in promotion of growth and acquisition of learning ability. If applied properly to human, inhalable GH would be effective for growth promotion and possibly for several disorders caused by under expression of NMDA receptors.(Endocrinology 151: 4418-4427,2010)

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