Activity, Motor Control & Coordination
Pain - Thermal Allodynia / Hyperalgesia
Pain - Spontaneous Pain - Postural Deficit
Pain - Mechanical Allodynia / Hyperalgesia
Anxiety & Depression Disorder
Learning/Memory - Attention - Addiction
Physiology & Respiratory Research
Metabolism - Food & Drink Intake
Pain
Central Nervous System (CNS)
Neurodegeneration
Sensory system
Motor control
Mood Disorders
Other disorders
Muscular system
Joints
Metabolism
Cross-disciplinary subjects
Preclinical studies and opioids: role in crisis management in the United States Authors
F Nishida, CN Zanuzzi, MS Sisti, E Falomir Lockhart et al
Lab
Facultad de Ciencias Veterinarias, Universidad Nacional de La Plata, La Plata, Argentina.
Journal
European Journal of Neuroscience
Abstract
Development of alternative therapies for treating functional deficits after different neurological damages is a challenge in neuroscience. Insulin_like growth factor_1 (IGF_1) is a potent neurotrophic factor exerting neuroprotective actions in brain and spinal cord. It is used to prevent or treat injuries of the central nervous system using different administration routes in different animal models. In this study, we evaluated whether intracisternal (IC) route for IGF_1 gene therapy may abrogate or at least reduce the structural and behavioral damages induced by the intraparenchymal injection of kainic acid (KA) into the rat spinal cord. Experimental (Rad_IGF_1) and control (Rad_DsRed_KA) rats were evaluated using a battery of motor and sensory tests before the injection of the recombinant adenovector (day _3), before KA injection (day 0) and at every post_injection (pi) time point (days 1, 2, 3 and 7 pi). Histopathological changes and neuronal and glial counting were assessed. Pretreatment using IC delivery of RAd_IGF_1 improved animal's general condition and motor and sensory functions as compared to Rad_DsRed_KA_injected rats. Besides, IC Rad_IGF_1 therapy abrogated later spinal cord damage and reduced the glial response induced by KA as observed in Rad_DsRed_KA rats. We conclude that the IC route for delivering RAd_IGF_1 prevents KA_induced excitotoxicity in the spinal cord.
