» Articles » PMID: 27246998

Developmental Plasticity in the Neural Control of Breathing

Overview
Journal Exp Neurol
Specialty Neurology
Date 2016 Jun 2
PMID 27246998
Citations 16
Authors
Affiliations
Soon will be listed here.
Abstract

The respiratory control system undergoes a diversity of morphological and physiological transformational stages during intrauterine development as it prepares to transition into an air-breathing lifestyle. Following birth, the respiratory system continues to develop and may pass through critical periods of heightened vulnerability to acute environmental stressors. Over a similar time course, however, the developing respiratory control system exhibits substantial capacity to undergo plasticity in response to chronic or repeated environmental stimuli. A hallmark of developmental plasticity is that it requires an interaction between a stimulus (e.g., hypoxia, hyperoxia, or psychosocial stress) and a unique window of development; the same stimulus experienced beyond the boundaries of this critical window of plasticity (e.g., at maturity), therefore, will have little if any appreciable effect on the phenotype. However, there are major gaps in our understanding of the mechanistic basis of developmental plasticity. Filling these gaps in our knowledge may be crucial to advancing our understanding of the developmental origin of adult health and disease. In this review, we: i) begin by clarifying some ambiguities in the definitions of plasticity and related terms that have arisen in recent years; ii) describe various levels of the respiratory control system where plasticity can (or has been identified to) occur; iii) emphasize the importance of understanding the mechanistic basis of developmental plasticity; iv) consider factors that influence whether developmental plasticity is permanent or whether function can be restored; v) discuss genetic and sex-based variation in the expression of developmental plasticity; and vi) provide a translational perspective to developmental plasticity.

Citing Articles

Respiratory plasticity induced by chronic hyperoxia in juvenile and adult rats.

Bavis R, Danielson M, Dufour G, Hanus J, Pratt A, Tobin K Respir Physiol Neurobiol. 2024; 333:104386.

PMID: 39732308 PMC: 11829821. DOI: 10.1016/j.resp.2024.104386.


Recovery of ventilatory and metabolic responses to hypoxia in neonatal rats after chronic hypoxia.

Bavis R, Lee D, Kinnally A, Buxton P Respir Physiol Neurobiol. 2024; 329:104317.

PMID: 39187051 PMC: 11385746. DOI: 10.1016/j.resp.2024.104317.


Real-time changes in rib cage expansion and use of abdominal mechanical stimulation in newborns: a quasi-experimental study.

Santos J, Silva P, Cruz M, Silva B, Guerra Azevedo I, Pereira S Rev Paul Pediatr. 2023; 42:e2023032.

PMID: 38126599 PMC: 10742371. DOI: 10.1590/1984-0462/2024/42/2023032.


Maturation of cardioventilatory physiological trajectories in extremely preterm infants.

Weese-Mayer D, Di Fiore J, Lake D, Hibbs A, Claure N, Qiu J Pediatr Res. 2023; 95(4):1060-1069.

PMID: 37857848 PMC: 11580183. DOI: 10.1038/s41390-023-02839-0.


Efficacy of verbascoside, echinacoside, crenatoside on altitude-induced fatigue in rats and possible mechanism.

Ziliang G, Qingyuan Q, Xiaolin L, Yuting Z, Jun R, Maoxing L J Tradit Chin Med. 2023; 43(5):934-943.

PMID: 37679981 PMC: 10465824. DOI: 10.19852/j.cnki.jtcm.20230630.001.