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毒蕈碱受体刺激可增强大鼠唾液腺功能对辐射损伤的耐受性。

Muscarinic receptor stimulation increases tolerance of rat salivary gland function to radiation damage.

作者信息

Coppes R P, Vissink A, Zeilstra L J, Konings A W

机构信息

Department of Radiobiology, University of Groningen, The Netherlands.

出版信息

Int J Radiat Biol. 1997 Nov;72(5):615-25. doi: 10.1080/095530097143112.

DOI:10.1080/095530097143112
PMID:9374441
Abstract

PURPOSE

To investigate if muscarinic receptor-stimulated activation of the PLC/PIP2 second messenger pathway prior to irradiation increases the radiotolerance of rat salivary gland.

MATERIALS AND METHODS

Rats were treated with pilocarpine, methacholine, reserpine, methacholine plus reserpine, or atropine prior to irradiation with a single dose of 15 Gy X-rays. Parotid and submandibular/sublingual saliva was collected 4 days before and 1-30 days after irradiation. Lag phase, flow rate, amylase secretion, and salivary sodium and potassium concentration were measured.

RESULTS

Pretreatment with pilocarpine or methacholine resulted in an improvement of all measured functions of both glands. Pretreatment with reserpine had no effect on parotid gland function. Reserpine plus methacholine did not increase parotid gland function when compared with methacholine alone, indicating a purely muscarinic receptor stimulation as the initiator for the induced radioprotection. Pretreatment protective effects on submandibular gland function of reserpine plus methacholine were additive, indicating cooperation of muscarinic and alpha-adrenergic receptors. Atropine pretreatment slightly increased the radiation induced loss of salivary gland function.

CONCLUSIONS

Preirradiation activation of PLC/PIP2 second messenger pathway through stimulation of muscarinic receptors reduces the salivary gland radiosensitivity. The observed protection of salivary gland function may be of a secondary nature, implicating a cell conditioning after receptor stimulation of the PLC/PIP2 pathway.

摘要

目的

研究在照射前通过毒蕈碱受体刺激磷脂酶C/磷脂酰肌醇-4,5-二磷酸(PLC/PIP2)第二信使途径是否能增加大鼠唾液腺的放射耐受性。

材料与方法

大鼠在接受单次15 Gy X射线照射前,分别用毛果芸香碱、乙酰甲胆碱、利血平、乙酰甲胆碱加 利血平或阿托品进行处理。在照射前4天以及照射后1至30天收集腮腺和颌下腺/舌下腺的唾液。测量延迟期、流速、淀粉酶分泌以及唾液中钠和钾的浓度。

结果

用毛果芸香碱或乙酰甲胆碱预处理可改善两个腺体所有测量的功能。用利血平预处理对腮腺功能无影响。与单独使用乙酰甲胆碱相比,利血平加乙酰甲胆碱并未增强腮腺功能,表明单纯的毒蕈碱受体刺激是诱导放射防护的起始因素。利血平加乙酰甲胆碱对颌下腺功能的预处理保护作用具有相加性,表明毒蕈碱受体和α-肾上腺素能受体存在协同作用。阿托品预处理略微增加了辐射诱导的唾液腺功能丧失。

结论

照射前通过刺激毒蕈碱受体激活PLC/PIP2第二信使途径可降低唾液腺的放射敏感性。观察到的对唾液腺功能的保护可能是继发性的,这意味着在PLC/PIP2途径的受体刺激后存在细胞适应性改变。

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