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Selective accumulation of monoclonal antibodies against neurospecific enolase in brain tissue of rats with middle cerebral artery occlusion
Authors:V.?P.?Chekhonin,S.?V.?Lebedev,I.?A.?Ryabukhin,S.?V.?Petrov,O.?I.?Gurina  author-information"  >  author-information__contact u-icon-before"  >  mailto:gurina@fport.ru"   title="  gurina@fport.ru"   itemprop="  email"   data-track="  click"   data-track-action="  Email author"   data-track-label="  "  >Email author,T.?B.?Dmitrieva,A.?I.?Volkov,I.?A.?Kashparov,Yu.?S.?Skoblov
Affiliation:(1) V. P. Serbskii State Research Center for Social and Forensic Psychiatry, Moscow;(2) Institute of Protein, Russian Academy of Sciences, Pushchino;(3) V. A. Engel"rsquo"gardt Institute of Molecular Biology, Russian Academy of Sciences, Moscow.
Abstract:Preparations of I125-labeled monoclonal antibodies against neurospecific enolase and mouse plasma IgG1 were injected intravenously to rats immediately after unilateral occlusion of the middle cerebral artery. Radioactivity of I125-labeled monoclonal antibodies against neurospecific enolase in the brain tissue progressively increased, reached a maximum by the 48th hour, and remained practically unchanged after 72 h. At the same time radioactivity of labeled IgG1 in the brain tissue and radioactivity of both preparations in the blood, liver, spleen, kidneys, heart, and lungs decreased over 72 h. Selective accumulation of I125-labeled monoclonal antibodies against neurospecific enolase was less significant in the brain tissue of the contralateral hemisphere and cerebellum not exposed to ischemia.Translated from Byulletenrsquo Eksperimentalrsquonoi Biologii i Meditsiny, Vol. 138, No. 10, pp. 388–392, October, 2004
Keywords:I125-labeled monoclonal antibodies against neurospecific enolase and mouse IgG1  rats  organ distribution  unilateral occlusion of middle cerebral artery
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