On the effect of chemically activated fine muscle afferents on interneurones mediating group I non-reciprocal inhibition of extensor ankle and knee muscles in humans

التفاصيل البيبلوغرافية
العنوان: On the effect of chemically activated fine muscle afferents on interneurones mediating group I non-reciprocal inhibition of extensor ankle and knee muscles in humans
المؤلفون: B. Decchi, V Groccia, S Dami, Alessandro Rossi, R Della Volpe
المصدر: Brain research. 815(1)
سنة النشر: 1999
مصطلحات موضوعية: Pain, Stimulation, Ascorbic Acid, Inhibitory postsynaptic potential, Antioxidants, Membrane Potentials, H-Reflex, Interneurons, Conditioning, Psychological, medicine, Humans, Membrane conductance, Knee, Neurons, Afferent, Muscle, Skeletal, Molecular Biology, Motor Neurons, Chemistry, musculoskeletal, neural, and ocular physiology, General Neuroscience, Reciprocal inhibition, Nociceptors, Neural Inhibition, Hyperpolarization (biology), medicine.anatomical_structure, Nociception, nervous system, Disinhibition, Neurology (clinical), Ankle, medicine.symptom, Neuroscience, Femoral Nerve, Developmental Biology
الوصف: In a previous paper it was shown that muscle nociceptive discharge depressed the activity of interneurones mediating group I non-reciprocal inhibition (or Ib interneurones) in humans [A. Rossi, B. Decchi, Changes in Ib heteronymous inhibition to soleus motoneurons during cutaneous and muscle nociceptive stimulation in humans, Brain Res. 774 (1997) 55-61.]. However, since nociceptive discharge depressed the size of the soleus H-reflex (by which Ib inhibition was tested) the question arises as to whether modification of motoneurone membrane conductance per se could depress the size of Ib inhibitory post-synaptic potentials. The results of the present study suggest that the contribution of motoneurone hyperpolarization to Ib disinhibition is negligible and that muscle nociceptive discharge actually depresses the activity of these pathways.
تدمد: 0006-8993
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c7e889461bc38e044796769bd59e987
https://pubmed.ncbi.nlm.nih.gov/9974128
حقوق: OPEN
رقم الأكسشن: edsair.doi.dedup.....3c7e889461bc38e044796769bd59e987
قاعدة البيانات: OpenAIRE