Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1-2
pubmed:dateCreated
1997-2-13
pubmed:abstractText
Interleukin-6 (IL-6), a multipotential cytokine, initiates signal transduction pathways similar to those of ciliary neurotrophic factor (CNTF) and leukemia inhibitory factor (LIF). These molecules share the signal transducing receptor component, gp130. IL-6 triggers homodimerization of gp130, whereas CNTF and LIF induce heterodimerization of gp130 and LIF receptor. Although CNTF or LIF treatment attenuates motor deficits in wobbler mouse motor neuron disease (MND), neuroprotective effects of IL-6 on this animal have not yet been clarified. Here we studied whether simultaneous treatment with IL-6 and soluble IL-6 receptor (sIL-6R) can ameliorate symptomatic and neuropathological changes in wobbler mouse MND. After clinical diagnosis at postnatal age 3-4 weeks, wobbler mice received subcutaneous injection with human recombinant IL-6 (1.0 mg/kg), human sIL-6R (0.5 mg/kg), IL-6 + sIL-6R or vehicle, daily for 4 weeks in a blind fashion. Compared to vehicle, coadministration with IL-6 and sIL-6R potentiated grip strength, attenuated muscle contractures in the forelimbs, reduced denervation muscle atrophy and prevented degeneration of spinal motor neurons. Single administration with IL-6 or sIL-6R did not retard the symptomatic and neuropathological progression, although IL-6-treated mice did not raise anti-IL-6 antibodies. Treatment with IL-6 + sIL-6R, but not with IL-6 or sIL-6R alone delayed progression of wobbler mouse MND. Our results indicate that the neuroprotective mechanism for IL-6/sIL-6R on wobbler mouse MND differs from that of CNTF or LIF alone. We hypothesize that IL-6/sIL-6R complex may function on motor neurons through activation and homodimerization of gp130.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jul
pubmed:issn
0006-8993
pubmed:author
pubmed:issnType
Print
pubmed:day
8
pubmed:volume
726
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
91-7
pubmed:dateRevised
2003-11-14
pubmed:meshHeading
pubmed-meshheading:8836549-Animals, pubmed-meshheading:8836549-Antibodies, Monoclonal, pubmed-meshheading:8836549-Antigens, CD, pubmed-meshheading:8836549-Cell Count, pubmed-meshheading:8836549-Disease Progression, pubmed-meshheading:8836549-Drug Evaluation, Preclinical, pubmed-meshheading:8836549-Interleukin-6, pubmed-meshheading:8836549-Mice, pubmed-meshheading:8836549-Mice, Neurologic Mutants, pubmed-meshheading:8836549-Motor Neuron Disease, pubmed-meshheading:8836549-Motor Neurons, pubmed-meshheading:8836549-Muscle, Skeletal, pubmed-meshheading:8836549-Neuroprotective Agents, pubmed-meshheading:8836549-Receptors, Interleukin, pubmed-meshheading:8836549-Receptors, Interleukin-6, pubmed-meshheading:8836549-Recombinant Proteins, pubmed-meshheading:8836549-Solubility, pubmed-meshheading:8836549-Spinal Cord
pubmed:year
1996
pubmed:articleTitle
Coadministration of interleukin-6 (IL-6) and soluble IL-6 receptor delays progression of wobbler mouse motor neuron disease.
pubmed:affiliation
Fourth Department of Internal Medicine, Toho University Ohashi Hospital, Tokyo, Japan.
pubmed:publicationType
Journal Article