Coppes R P, Zeilstra L J, Kampinga H H, Konings A W
Department of Radiation and Stress Cell Biology, University of Groningen, Ant. Deusinglaan 1, 9713 AV Groningen, The Netherlands.
Br J Cancer. 2001 Sep 28;85(7):1055-63. doi: 10.1054/bjoc.2001.2038.
Damage to salivary glands after radiotherapeutic treatment of head and neck tumours can severely impair the quality of life of the patients. In the current study we have investigated the early-to-late pathogenesis of the parotid gland after radiation. Also the ability to ameliorate the damage using pretreatment with adrenergic or muscarinic receptor agonists is studied. Rats were locally irradiated with or without i.p. pretreatment with phenylephrine (alpha-adrenoceptor agonist, 5 mg kg(-1)), isoproterenol (beta-adrenoceptor agonist, 5 mg kg(-1)), pilocarpine (4 mg kg(-1)), methacholine (3.75 mg kg(-1)) (muscarinic receptor agonists) or methacholine plus phenylephrine. Parotid salivary flow rate, amylase secretion, the number of cells and gland histology were monitored sequentially up to 240 days postirradiation. The effects were described in 4 distinct phases. The first phase (0-10 days) was characterised by a rapid decline in flow rate without changes in amylase secretion or acinar cell number. The second phase (10-60 days) consists of a decrease in amylase secretion and is paralleled by acinar cell loss. Flow rate, amylase secretion and acinar cell numbers do not change in the third phase (60-120 days). The fourth phase (120-240 days) is determined by a further deterioration of gland function but an increase in acinar cell number, albeit with poor tissue morphology. All drug pretreatments used could reduce radiation effects in phase I and II. The protective effects were lost during phase IV, with the exception of methacholine plus phenylephrine pretreatment. The latter combination of drugs ameliorated radiation-damage throughout the entire follow-up time. The data show that combined pre-irradiation stimulation of muscarinic acetylcholine receptors with methacholine plus alpha-adrenoceptors with phenylephrine can reduce both early and late damage, possibly involving the PLC/PIP2 second messenger pathways. This opens perspectives for the development of clinical applicable methods for long-term sparing of parotid glands subjected to radiotherapy of head and neck cancer patients.
对头颈部肿瘤进行放射治疗后,唾液腺受损会严重损害患者的生活质量。在本研究中,我们调查了腮腺在辐射后的早期至晚期发病机制。同时还研究了使用肾上腺素能或毒蕈碱受体激动剂进行预处理改善损伤的能力。对大鼠进行局部照射,部分大鼠在照射前腹腔注射去氧肾上腺素(α-肾上腺素能受体激动剂,5 mg·kg⁻¹)、异丙肾上腺素(β-肾上腺素能受体激动剂,5 mg·kg⁻¹)、毛果芸香碱(4 mg·kg⁻¹)、乙酰甲胆碱(3.75 mg·kg⁻¹)(毒蕈碱受体激动剂)或乙酰甲胆碱加去氧肾上腺素进行预处理。在照射后长达240天的时间内,依次监测腮腺唾液流速、淀粉酶分泌、细胞数量和腺体组织学。这些效应可分为4个不同阶段。第一阶段(0 - 10天)的特征是流速迅速下降,而淀粉酶分泌或腺泡细胞数量无变化。第二阶段(10 - 60天)淀粉酶分泌减少,同时腺泡细胞丢失。第三阶段(60 - 120天)流速、淀粉酶分泌和腺泡细胞数量均无变化。第四阶段(120 - 240天)的特点是腺体功能进一步恶化,但腺泡细胞数量增加,尽管组织形态较差。所有使用的药物预处理均可在第一和第二阶段减轻辐射效应。在第四阶段,除乙酰甲胆碱加去氧肾上腺素预处理外,其他预处理的保护作用均消失。后一种药物组合在整个随访期间均能改善辐射损伤。数据表明,辐射前联合使用乙酰甲胆碱刺激毒蕈碱型乙酰胆碱受体和去氧肾上腺素刺激α-肾上腺素能受体可减少早期和晚期损伤,可能涉及磷脂酶C/磷脂酰肌醇-4,5-二磷酸(PLC/PIP2)第二信使途径。这为开发临床适用方法以长期保护接受头颈癌放疗患者的腮腺开辟了前景。