Please use this identifier to cite or link to this item: https://hdl.handle.net/20.500.12202/3325
Title: The provision of precursors for acetylcholine synthesis
Authors: Schein, Joshua David
Keywords: Neurosciences.
Biology.
Issue Date: 1990
Publisher: ProQuest Dissertations & Theses
Citation: Source: Dissertation Abstracts International, Volume: 51-05, Section: B, page: 2222.;Advisors: Peter Davies.
Abstract: This thesis, consisting of three chapters, is a study of the supply of precursors for acetylcholine synthesis.;Chapter 1 examines acetylcholine synthesis in a human neuroblastoma cell line, MC-IXC. Synthesis rates were measured using various radiolabelled precursors for the acetyl moiety. (2-{dollar}\sp{lcub}14{rcub}{dollar}C) Pyruvate was the most effective precursor, yielding rates of synthesis approaching the maximal rates observed in cell homogenates. (U-{dollar}\sp{lcub}14{rcub}{dollar}C) Glucose, 3-hydroxy (3-{dollar}\sp{lcub}14{rcub}{dollar}C) butyrate, (2-{dollar}\sp{lcub}14{rcub}{dollar}) acetate, and (1,5-{dollar}\sp{lcub}14{rcub}{dollar}C) citrate could all serve as precursors, but synthesis rates were much lower using these compounds. The results suggest that the rate of acetylcholine synthesis in MC-IXC cells is limited by the rate of glycolysis.;Chapters 2 and 3 describe an attempt to generate antibodies to the high-affinity choline uptake system (HAChTS) via an anti-idiotypic route. Monoclonal and polyclonal antibodies were generated to the choline uptake inhibitor hemicholinium-3. These antibodies were then used to generate monoclonal and polyclonal anti-idiotypic antibodies. Five of the anti-idiotypic antibodies inhibited the uptake of ({dollar}\sp3{dollar}H) choline into rat brain synaptosomes. Immunocytochemistry using four of the antibodies revealed a staining pattern in hippocampus consistent with the known distribution of cholinergic terminals. The results suggest that these antibodies recognize the HACHTS.
URI: https://ezproxy.yu.edu/login?url=http://gateway.proquest.com/openurl?url_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:dissertation&res_dat=xri:pqm&rft_dat=xri:pqdiss:9029095
https://hdl.handle.net/20.500.12202/3325
Appears in Collections:Albert Einstein College of Medicine: Doctoral Dissertations

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