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. 1967 Jan;188(1):1-11.
doi: 10.1113/jphysiol.1967.sp008119.

Motor responses of the urinary bladder and skeletal muscle in botulinum intoxicated rats

Motor responses of the urinary bladder and skeletal muscle in botulinum intoxicated rats

F G Carpenter. J Physiol. 1967 Jan.

Abstract

1. Type A or type D botulinum toxin administered to rats did not produce a generalized paralysis of skeletal muscles at the time of ventilatory arrest. However, if survival was extended by artificial ventilation complete blockade of neuromuscular transmission developed 6.5 hr after 100 MLD of type D and 5 hr after 1000 MLD of type A toxin. The onset of paralysis of a muscle was shortened by repetitive stimulation of the motor nerves.2. There was no consistent blockade of parasympathetically innervated viscera in animals dying after type A toxin. Animals given type D toxin displayed mydriasis and urinary retention before death.3. Motor responses to electrical stimulation, of bladder preparations in vitro were more vulnerable to type D than to type A toxin. When somatic paralysis was complete in animals treated with type A or type D toxin the excised bladders produced pressure elevations 45 and 25%, respectively, of control preparations.4. During electrical stimulation of bladder preparations nearly paralysed by either toxin, the ACh release was significantly diminished from controls. In the rat bladder botulinum toxin specifically disrupted the liberation of mediator from post-ganglionic nerve endings.

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References

    1. J Physiol. 1954 Mar 29;123(3):501-15 - PubMed
    1. Pharmacol Rev. 1955 Dec;7(4):467-94 - PubMed
    1. Am J Hyg. 1955 Jul;62(1):21-8 - PubMed
    1. J Physiol. 1962 Feb;160:221-33 - PubMed
    1. J Physiol. 1949 Aug;109(1-2):10-24 - PubMed

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