From cerebral palsy to developmental coordination disorder: Development of preclinical rat models corresponding to recent epidemiological changes

Jacques-Olivier Coq (1) , Marine Kochmann (1) , Diego Lacerda (1, 2) , Hanane Khalki (1, 3) , Maxime S Delcour (4) , Ana Toscano (2) , Florence Cayetanot (1, 5) , Marie-Hélène Canu (6) , Mary F Barbe (7) , Masahiro Tsuji (8)

1 INT - Institut de Neurosciences de la Timone
2 UFPE - Universidade Federal de Pernambuco [Recife]
3 USMS - Université Sultan Moulay Slimane
4 UdeM - Université de Montréal
5 UMRS 1158 - Neurophysiologie Respiratoire Expérimentale et Clinique
6 URePSSS - Unité de Recherche Pluridisciplinaire Sport, Santé, Société (URePSSS) - ULR 7369 - ULR 4488
7 Temple University [Philadelphia]
8 Kyoto Women's University

Cerebral palsy (CP) is a complex syndrome of various sensory, motor and cognitive deficits. Its prevalence has recently decreased in some developed countries and its symptoms have also shifted since the 1960s. From the 1990s, CP has been associated with prematurity, but recent epidemiologic studies show reduced or absent brain damage, which recapitulates developmental coordination disorder (DCD). In previous studies, we developed a rat model based on mild intrauterine hypoperfusion (MIUH) that recapitulated the diversity of symptoms observed in preterm survivors. Briefly, MIUH led to early inflammatory processes, diffuse brain damage, minor locomotor deficits, musculoskeletal pathologies, neuroanatomical and functional disorganization of the primary somatosensory (S1) cortex but not in the motor cortex (M1), delayed sensorimotor reflexes, spontaneous hyperactivity, deficits in sensory information processing, and memory and learning impairments in adult rats. Adult MIUH rats also exhibited changes in muscle contractile properties and phenotype, enduring hyperreflexia and spasticity, as well as hyperexcitability in the sensorimotor cortex. We recently developed a rat model of DCD based on postnatal sensorimotor restriction (SMR) without brain damage. Briefly, SMR led to digitigrade locomotion (i.e., “toe walking”) related to ankle-knee overextension, degraded musculoskeletal tissues (e.g., gastrocnemius atrophy), and lumbar hyperreflexia. The postnatal SMR then led to secondary degradation of the hind-limb maps in S1 and M1 cortices, altered cortical response properties and cortical hyperexcitability, but no brain damage. Thus, our 2 rat models appear to recapitulate the diversity of symptoms ranging from CP to DCD and contribute to understanding the emergence and mechanisms underlying the corresponding neurodevelopmental disorders. These preclinical models seem promising for testing strategies of rehabilitation based on both physical and cognitive training to promote adaptive brain plasticity and to improve physical body conditions.

Mots clés: Cerebral palsy; Developmental Coordination Disorder; Hypoperfusion; Intrauterine growth retardation; Prematurity; Sensorimotor restriction; White matter injury

Domaines: Neurobiologie

Jacques-Olivier Coq, Marine Kochmann, Diego Lacerda, Hanane Khalki, Maxime S Delcour, et al.. From cerebral palsy to developmental coordination disorder: Development of preclinical rat models corresponding to recent epidemiological changes. Annals of Physical and Rehabilitation Medicine, 2019, ⟨10.1016/j.rehab.2019.10.002⟩. ⟨hal-02389594v2⟩