Milner P, Belai A, Tomlinson A, Hoyle C H, Sarner S, Burnstock G
Department of Anatomy and Developmental Biology, University College London, UK.
J Pharm Pharmacol. 1992 Sep;44(9):777-9. doi: 10.1111/j.2042-7158.1992.tb05520.x.
In order to investigate the toxic effects of long-term treatment with anthraquinone laxatives, rats were fed either chocolate alone, or chocolate adulterated with senna or danthron (1,8-dihydroxyanthraquinone) for 5 months. Mesenteric blood vessels and the outer muscle layers of the caecum, together with the myenteric plexus, were examined using ultrastructural, histochemical, immunohistochemical and immunoassay techniques. There was no ultrastructural evidence of degeneration in either the mesenteric vessels or the caecum. In the mesenteric vessels, levels of neuropeptide Y were significantly reduced in the danthron-fed rats, but levels of substance P (SP), calcitonin gene-related peptide (CGRP) and vasoactive intestinal polypeptide (VIP) were unaffected by all treatments. In the caecum, VIP-, SP- and CGRP-immunoreactivity and catecholamine-fluorescence were unchanged by the laxative treatments.
为了研究长期使用蒽醌类泻药的毒性作用,将大鼠分为三组,分别喂食单纯巧克力、掺有番泻叶的巧克力或掺有丹蒽醌(1,8 - 二羟基蒽醌)的巧克力,持续5个月。使用超微结构、组织化学、免疫组织化学和免疫测定技术对肠系膜血管、盲肠外肌层以及肌间神经丛进行检查。无论是肠系膜血管还是盲肠,均未发现超微结构退变的证据。在肠系膜血管中,喂食丹蒽醌的大鼠体内神经肽Y水平显著降低,但P物质(SP)、降钙素基因相关肽(CGRP)和血管活性肠肽(VIP)的水平不受所有处理的影响。在盲肠中,泻药处理后VIP、SP和CGRP免疫反应性以及儿茶酚胺荧光均未改变。