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1.
FASEB J ; 35(2): e21214, 2021 02.
Artículo en Inglés | MEDLINE | ID: mdl-33236396

RESUMEN

Neonatal brachial plexus injury (NBPI) causes disabling and incurable contractures, or limb stiffness, which result from proteasome-mediated protein degradation impairing the longitudinal growth of neonatally denervated muscles. We recently showed in a mouse model that the 20S proteasome inhibitor, bortezomib, prevents contractures after NBPI. Given that contractures uniquely follow neonatal denervation, the current study tests the hypothesis that proteasome inhibition during a finite window of neonatal development can prevent long-term contracture development. Following neonatal forelimb denervation in P5 mice, we first outlined the minimum period for proteasome inhibition to prevent contractures 4 weeks post-NBPI by treating mice with saline or bortezomib for varying durations between P8 and P32. We then compared the ability of varying durations of longer-term proteasome inhibition to prevent contractures at 8 and 12 weeks post-NBPI. Our findings revealed that proteasome inhibition can be delayed 3-4 days after denervation but is required throughout skeletal growth to prevent contractures long term. Furthermore, proteasome inhibition becomes less effective in preventing contractures beyond the neonatal period. These therapeutic effects are primarily associated with bortezomib-induced attenuation of 20S proteasome ß1 subunit activity. Our collective results, therefore, demonstrate that temporary neonatal proteasome inhibition is not a viable strategy for preventing contractures long term. Instead, neonatal denervation causes a permanent longitudinal growth deficiency that must be continuously ameliorated during skeletal growth. Additional mechanisms must be explored to minimize the necessary period of proteasome inhibition and reduce the risk of toxicity from long-term treatment.


Asunto(s)
Bortezomib/uso terapéutico , Contractura/prevención & control , Parálisis Neonatal del Plexo Braquial/tratamiento farmacológico , Inhibidores de Proteasoma/uso terapéutico , Animales , Bortezomib/administración & dosificación , Bortezomib/farmacología , Contractura/tratamiento farmacológico , Ratones , Parálisis Neonatal del Plexo Braquial/prevención & control , Complejo de la Endopetidasa Proteasomal/metabolismo , Inhibidores de Proteasoma/administración & dosificación , Inhibidores de Proteasoma/farmacología , Sarcómeros/efectos de los fármacos , Sarcómeros/metabolismo
2.
Medicine (Baltimore) ; 99(34): e21830, 2020 Aug 21.
Artículo en Inglés | MEDLINE | ID: mdl-32846828

RESUMEN

Brachial plexus birth palsy (BPBP) is a neurologic injury that can result in mild to full paralysis of the affected upper extremity. In severe cases, nerve surgery is often performed before age 1 year. Several studies report gains in elbow flexion with onabotulinum toxin type A (OBTT-A) injections to the triceps; however, its use in infants is not widely reported. The purpose of this study is to present our experience using these injections before 6 months of age to therapeutically unmask elbow flexion and diagnostically guide surgical decision making.This is a retrospective observational cohort study. The cohort included infants with BPBP who received OBTT-A injection to the triceps before age 6 months. Indications for the injections include trace elbow flexion and palpable co-contraction of the biceps and triceps. Elbow flexion was evaluated using the Toronto Test score. Therapeutic success was defined as an increase in post-injection scores. These scores were then used diagnostically as an indication for surgery if the infant did not achieve full elbow flexion by 8 months. A treatment algorithm for OBTT-A triceps injection was developed based on all treatment options offered to infants with elbow flexion deficits seen in the clinic.Of the 12 infants that received OBTT-A triceps injections, 10 (83%) had improved Toronto test elbow flexion scores post-injection. Gains in elbow flexion once attained were maintained. Of the 9 OBTT-A infants with at least 2 years follow-up, 4 achieved full elbow flexion without surgery; the remainder after surgery. No complications with OBTT-A injections were noted and patients were followed on average 6 years. The average age at time of injection was 4 months (range: 2-5 months). Compared to other treatments given, OBTT-A infants tended to present with more elbow flexion than the 4 infants requiring immediate surgical intervention and less elbow flexion than the 16 infants treated conservatively.OBTT-A injection to the triceps in infants with BPBP before 6 months of age therapeutically improved elbow flexion and diagnostically guided surgical decisions when full elbow flexion was not achieved by 8 months of age with no known complications.


Asunto(s)
Toxinas Botulínicas Tipo A/uso terapéutico , Articulación del Codo/fisiopatología , Músculo Esquelético/fisiopatología , Parálisis Neonatal del Plexo Braquial/tratamiento farmacológico , Fármacos Neuromusculares/uso terapéutico , Rango del Movimiento Articular/efectos de los fármacos , Brazo , Toxinas Botulínicas Tipo A/administración & dosificación , Niño , Preescolar , Toma de Decisiones Clínicas , Estudios de Seguimiento , Humanos , Lactante , Inyecciones Intramusculares , Parálisis Neonatal del Plexo Braquial/fisiopatología , Parálisis Neonatal del Plexo Braquial/cirugía , Fármacos Neuromusculares/administración & dosificación , Estudios Retrospectivos
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