Journal article
DEFICIT OF SPINAL-CORD GLYCINE STRYCHNINE RECEPTORS IN INHERITED MYOCLONUS OF POLL HEREFORD CALVES
AL GUNDLACH, PR DODD, CSG GRABARA, WEJ WATSON, GAR JOHNSTON, PAW HARPER, JA DENNIS, PJ HEALY
SCIENCE | AMER ASSOC ADVANCEMENT SCIENCE | Published : 1988
Abstract
Inherited myoclonus of Poll Hereford calves is characterized by hyperesthesia and myoclonic jerks of the skeletal musculature, which occur spontaneously and in response to sensory stimuli. The disease shows autosomal recessive inheritance, and significant proportions of the Poll Hereford herds in many countries are thought to be carriers of the mutant gene. Studies revealed a specific and marked (90 to 95 percent) deficit in [3H]strychnine binding sites in spinal cord membranes from myoclonic animals compared to controls, reflecting a loss of, or defect in, glycine/strychnine receptors. Spinal cord synaptosomes prepared from affected animals showed a significantly increased ability to accumu..
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