Summary
The effect of physostigmine salicylate (0.5 mg/kg, i.p.) alone and in combination with atropine sulfate (25 mg/kg, i. p.) on levels of acetylcholine (ACh) and choline (Ch) and turnover of ACh has been studied in whole brain and striatum of mice. The animals were killed by focussed microwave irradiation and the turnover of ACh was studied after i.v. injection of deuterium labelled Ch by employing mass fragmentography. Physostigmine increased the levels of ACh in whole brain from 24.5–28.0 nmol/g (P<0.001) whereas there was no significant increase in striatum. The levels of Ch were also increased. The turnover rate of ACh was decreased in whole brain from 15.4 to 8.4 and in striatum from 52.9 to 24.4 nmol/g · min. Physostigmine given before or after atropine did not completely block the ACh lowering effect of atropine. When atropine was given before physostigmine the turnover rate of ACh in whole brain was increased to 24.2 nmoles/g · min. The results seem to indicate that there is no clear cut relation between the turnover rate and level of ACh in vivo. The increase of the turnover rate induced by atropine is masked unless a cholinesterase inhibitor is given to protect the newly synthesized labelled ACh released by atropine.
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A preliminary account of this work was reported at the Symposium on Current Topics in Drug Research, held October 19–21, 1977, at Uppsala, Sweden
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Karlén, B., Lundgren, G., Lundin, J. et al. Effect of physostigmine and atropine on acetylcholine turnover in mouse brain. Naunyn-Schmiedeberg's Arch. Pharmacol. 308, 61–65 (1979). https://doi.org/10.1007/BF00499720
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DOI: https://doi.org/10.1007/BF00499720