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P021

Peptide 021, GLXC-21260

Quick Stats
Studies 37
Trials 57
Score 1
2013 pubmed 24 citations

Postnatal development of brain-derived neurotrophic factor (BDNF) and tyrosine protein kinase B (TrkB) receptor immunoreactivity in multiple brain stem respiratory-related nuclei of the rat.

Liu. Qiuli Q; Wong-Riley. Margaret T T MT

Key Findings

  • BDNF and TrkB levels fall significantly at post‑natal day 12 in several brain‑stem breathing centers
  • Levels return to near‑baseline by day 14, suggesting a brief critical window
  • Non‑respiratory brain area (cuneate nucleus) shows only minor changes

Practical Outcomes

  • For now, the study is mostly basic science and doesn’t give direct actions for health‑optimizers. It hints that BDNF may play a role in breathing control, but there’s no proven way to use this information for human protocols yet.

Summary

In baby rats, the brain chemicals BDNF and its receptor TrkB drop sharply around day 12 in brain areas that control breathing, which may explain why their response to low oxygen is weakest then. The levels bounce back by day 14, and other brain regions show different patterns of change.

Abstract

Previously, we found a transient imbalance between suppressed excitation and enhanced inhibition in the respiratory network of the rat around postnatal days (P) 12-13, a critical period when the hypoxic ventilatory response is at its weakest. The mechanism underlying the imbalance is poorly understood. Brain-derived neurotrophic factor (BDNF) and its tyrosine protein kinase B (TrkB) receptors are known to potentiate glutamatergic and attenuate gamma-aminobutyric acid (GABA)ergic neurotransmission, and BDNF is essential for respiratory development. We hypothesized that the excitation-inhibition imbalance during the critical period stemmed from a reduced expression of BDNF and TrkB at that time within respiratory-related nuclei of the brain stem. An in-depth, semiquantitative immunohistochemical study was undertaken in seven respiratory-related brain stem nuclei and one nonrespiratory nucleus in P0-21 rats. The results indicate that the expressions of BDNF and TrkB: 1) in the pre-Bötzinger complex, nucleus ambiguus, commissural and ventrolateral subnuclei of solitary tract nucleus, and retrotrapezoid nucleus/parafacial respiratory group were significantly reduced at P12, but returned to P11 levels by P14; 2) in the lateral paragigantocellular nucleus and parapyramidal region were increased from P0 to P7, but were strikingly reduced at P10 and plateaued thereafter; and 3) in the nonrespiratory cuneate nucleus showed a gentle plateau throughout the first 3 postnatal weeks, with only a slight decline of BDNF expression after P11. Thus, the significant downregulation of both BDNF and TrkB in respiratory-related nuclei during the critical period may form the basis of, or at least contribute to, the inhibitory-excitatory imbalance within the respiratory network during this time.

Study Information

Provider

pubmed

Year

2013

Date

2013-01-01T00:00:00.000Z

DOI

10.1002/cne.23164

Citations

24

References

98