Intravenous administration of a transferrin receptor antibody-nerve growth factor conjugate prevents the degeneration of cholinergic striatal neurons in a model of Huntington disease

Proc Natl Acad Sci U S A. 1994 Sep 13;91(19):9077-80. doi: 10.1073/pnas.91.19.9077.

Abstract

Intrastriatal injections of quinolinic acid induce a pattern of neuronal degeneration similar to that seen in Huntington disease. In the present study, nerve growth factor (NGF) crossed the blood-brain barrier in a dose-dependent fashion following intravenous infusion when conjugated to an antibody directed against the transferrin receptor (OX-26). Intravenous injections of the OX-26-NGF conjugate selectively prevented the loss of striatal choline acetyltransferase-immunoreactive neurons which normally occurs following quinolinic acid administration relative to control rats receiving vehicle or a nonconjugated mixture of OX-26 and NGF. These data demonstrate that a neurotrophic factor-antibody conjugate can prevent the degeneration of central NGF-responsive neurons following systemic administration.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Antibodies, Monoclonal / administration & dosage
  • Corpus Striatum / pathology*
  • Huntington Disease / pathology
  • Huntington Disease / therapy*
  • Male
  • Nerve Degeneration
  • Nerve Growth Factors / administration & dosage*
  • Quinolinic Acid
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, Transferrin

Substances

  • Antibodies, Monoclonal
  • Nerve Growth Factors
  • Receptors, Transferrin
  • Quinolinic Acid