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Immunocytochemical identification of dynorphin-containing vesicles in Brattleboro rats
Authors:M H Whitnall  M Castel  S Key  H Gainer
Institution:1. Laboratory of Neurochemistry and Neuroimmunology, National Institute of Child Health and Human Development, National Institutes of Health, Bldg. 36, Rm. 2A21, Bethesda, MD 20205 USA;2. E.M. Unit, Institute of Life Sciences, Hebrew University of Jerusalem, Israel
Abstract:Vasopressin and its carrier protein, vasopressin-associated neurophysin, are co-packaged together with an opioid peptide, dynorphin, into 160 nm diameter neurosecretory vesicles in the normal rat hypothalamo-neurohypophysial system. The homozygous Brattleboro rat lacks vasopressin and vasopressin-associated neurophysin, but contains substantial amounts of dynorphin in the vasopressin-deficient neurosecretory cells. We used post-embedding electron microscopic immunocytochemistry to determine the subcellular location of dynorphin in Brattleboro rats. The results show that dynorphin is present within 100 nm neurosecretory vesicles in homozygous Brattleboro cell bodies and axons, and within 160 nm vesicles in heterozygous (control) neurosecretory cell bodies and axons. Oxytocin-associated neurophysin is present in a separate population of magnocellular neurons in both homozygous and heterozygous rats, and is contained within 160 nm vesicles in both cases. Therefore, the absence of synthesis of the vasopressin prohormone results in a dramatic reduction of neurosecretory vesicle size, despite the continued synthesis and packaging of dynorphin peptides.
Keywords:Dynorphin  Vasopressin  Oxytocin  Neurophysin  Brattleboro rat  Secretory vesicle  Electron microscopy  Immunocytochemistry
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