Opioid compounds, in addition to their analgesic and behavioral effects, have an important function in the regulation of growth particularly in developing neural systems. Although it is not known which of the endogenous neuropeptides are involved in this process, evidence indicates a prominent role for endorphin compounds.
The aim of the proposed studies is to identify the neuropeptides involved in cell development and to elucidate the mechanism(s) by which they express this control. We propose to characterize the effects of beta-endorphin and N alpha-acetyl-beta-endorphin on basal ornithine decarboxylase (ODC) activity on brain, liver, heart and kidney during ontogeny. ODC catalyzes the initial step in the synthesis of the polyamines, which are major regulators of macromolecular synthesis. The metabolic consequences of the changes in ODC will be assessed through evaluation of nucleic acid and protein synthesis. cAMP and tyrosine amino-transferase levels will be measured to determine whether the changes in ODC reflect a general alteration in cell metabolism or a specific intracellular action distal to cAMP generation. We will determine whether opioid and/or non-opioid mechanisms mediate these actions of neuropeptides. To establish whether neuropeptides influence development through actions on trophic hormones the effects of endorphins on plasma levels of insulin and growth hormone as well as on tissue sensitivity to these substances will be determined. To investigate whether the effects of neuropeptides on peripheral tissues are mediated by endocrine/neuronal signals originating in the CNS, similar studies will be conducted in hypophysectomized animals (as young as 4 days of age). These studies will clarify the role of the pituitary gland on developmental effects of neuropeptides. Finally, we will characterize the structural requirements of neuropeptides to elicit their actions on growth. Identification of the """"""""minimal"""""""" fragment of the neuropeptide molecule required to influence development as well as small peptide forms with potential growth-regulatory properties are expected from this part of the investigation. In summary, these studies will identify endogenous neuropeptides capable of regulating specific biochemical/endocrine/physiological processes intimately related to cell growth and development. These findings should provide important information for understanding events involved in normal and abnormal growth.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
5R01NS025738-03
Application #
3411128
Study Section
Neurological Sciences Subcommittee 1 (NLS)
Project Start
1988-02-01
Project End
1991-11-30
Budget Start
1990-02-01
Budget End
1991-11-30
Support Year
3
Fiscal Year
1990
Total Cost
Indirect Cost
Name
Duke University
Department
Type
Schools of Medicine
DUNS #
071723621
City
Durham
State
NC
Country
United States
Zip Code
27705
Bartolome, J V; Wang, S; Schanberg, S M et al. (1999) Involvement of c-myc and max in CNS beta-endorphin modulation of hepatic ornithine decarboxylase responsiveness to insulin in rat pups. Life Sci 64:PL87-91
Bartolome, J V; Wang, S; Greer, N L et al. (1999) Glucocorticoid regulation of ornithine decarboxylase in the postnatal rat lung. Life Sci 64:895-904
Bartolome, J V; Alicke, B; Bartolome, M B (1997) Central administration of morphine inhibits brain and liver ornithine decarboxylase activity in neonatal rats: involvement of transcription- and non-transcription-dependent mechanisms. Eur J Pharmacol 331:145-53
Wang, S; Bartolome, J V; Schanberg, S M (1996) Neonatal deprivation of maternal touch may suppress ornithine decarboxylase via downregulation of the proto-oncogenes c-myc and max. J Neurosci 16:836-42
Bartolome, J V; Chang, K J; Bartolome, M B (1995) The inhibition of ornithine decarboxylase activity in developing rat tissues by central nervous system beta-endorphin is mediated by mu-opioid receptors, but not by delta- or epsilon-opioid receptors. Eur J Pharmacol 284:43-50
Bartolome, J V; Wang, S; Bartolome, M B (1995) Transcription-dependent and -independent regulation of hepatic ornithine decarboxylase activity by CNS beta-endorphin in rat pups. Brain Res Mol Brain Res 33:149-56
Bartolome, J V; Bartolome, M B (1994) Role of the spinal cord in intracisternal beta-endorphin-evoked suppression of liver DNA synthesis in 10-day-old rats. Brain Res 642:311-5
Bartolome, J V; Lorber, B A; Bartolome, M B (1994) Brain cholecystokinin and beta-endorphin systems may antagonistically interact to regulate tissue DNA synthesis in rat pups. Brain Res 661:19-24
Bartolome, J V; Bartolome, M B; Lorber, B A et al. (1991) Effects of central administration of beta-endorphin on brain and liver DNA synthesis in preweanling rats. Neuroscience 40:289-94
Greer, N L; Schanberg, S M; Bartolome, J V (1991) Effect of central administration of beta-endorphin on lung ornithine decarboxylase activity in developing rats. Pediatr Res 29:182-6

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