Literature DB >> 1690752

Motor neuron destruction in guinea pigs immunized with bovine spinal cord ventral horn homogenate: experimental autoimmune gray matter disease.

J I Engelhardt1, S H Appel, J M Killian.   

Abstract

Guinea pigs immunized with bovine spinal cord ventral horn homogenate develop muscle weakness with electromyographic and morphologic evidence of denervation. Pathological examination demonstrates a loss of motoneurons and scattered inflammatory foci primarily localized to the spinal cord. Immunohistochemical techniques document the presence of immunoglobulin G at the motor end plate and around the external membrane and within the cytoplasm of motoneurons. This syndrome of experimental autoimmune gray matter disease (EAGMD) differs from experimental autoimmune motor neuron disease induced by inoculation with purified motoneurons and also differs from experimental autoimmune encephalomyelitis. The existence of two different forms of immune-mediated motoneuron destruction suggests that a number of cytoplasmic and membrane antigens may give rise to an immunologically based attack on the motor system.

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Year:  1990        PMID: 1690752     DOI: 10.1016/0165-5728(90)90132-7

Source DB:  PubMed          Journal:  J Neuroimmunol        ISSN: 0165-5728            Impact factor:   3.478


  6 in total

1.  Calcium current and charge movement of mammalian muscle: action of amyotrophic lateral sclerosis immunoglobulins.

Authors:  O Delbono; J García; S H Appel; E Stefani
Journal:  J Physiol       Date:  1991-12       Impact factor: 5.182

Review 2.  Immunological findings in amyotrophic lateral sclerosis.

Authors:  J P Antel; N R Cashman
Journal:  Springer Semin Immunopathol       Date:  1995

3.  The action of amyotrophic lateral sclerosis immunoglobulins on mammalian single skeletal muscle Ca2+ channels.

Authors:  V Magnelli; T Sawada; O Delbono; R G Smith; S H Appel; E Stefani
Journal:  J Physiol       Date:  1993-02       Impact factor: 5.182

4.  Immunoglobulins from animal models of motor neuron disease and from human amyotrophic lateral sclerosis patients passively transfer physiological abnormalities to the neuromuscular junction.

Authors:  S H Appel; J I Engelhardt; J García; E Stefani
Journal:  Proc Natl Acad Sci U S A       Date:  1991-01-15       Impact factor: 11.205

Review 5.  Nearly 30 Years of Animal Models to Study Amyotrophic Lateral Sclerosis: A Historical Overview and Future Perspectives.

Authors:  Tiziana Bonifacino; Roberta Arianna Zerbo; Matilde Balbi; Carola Torazza; Giulia Frumento; Ernesto Fedele; Giambattista Bonanno; Marco Milanese
Journal:  Int J Mol Sci       Date:  2021-11-12       Impact factor: 5.923

6.  Intraperitoneally administered IgG from patients with amyotrophic lateral sclerosis or from an immune-mediated goat model increase the levels of TNF-α, IL-6, and IL-10 in the spinal cord and serum of mice.

Authors:  Izabella Obál; Gergely Klausz; Yvette Mándi; Mária Deli; László Siklós; József I Engelhardt
Journal:  J Neuroinflammation       Date:  2016-05-24       Impact factor: 8.322

  6 in total

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