Zhang Wei-Wei, Li Yan, Wang Xue-Qing, Tian Feng, Cao Hong, Wang Min-Wei, Sun Qi-Shi
Department of Gastroenterology, the Second Affiliated Clinical Hospital of China Medical University, 36 Sanhao Street, Heping District, Shenyang 110004, Liaoning Province, China.
World J Gastroenterol. 2005 Jul 28;11(28):4414-8. doi: 10.3748/wjg.v11.i28.4414.
To study the effects of magnolol and honokiol on isolated smooth muscle of gastrointestinal tract and their relationship with Ca2+, and on the gastric emptying and the intestinal propulsive activity in mice.
Routine experimental methods using isolated gastric fundus strips of rats and isolated ileum segments of guinea pigs were adopted to measure the smooth muscle tension. The effects of magnolol 10(-3), 10(-4), 10(-5) mol/L, and honokiol 10(-4), 10(-5), 10(-6) mol/L on the contractility of gastric fundus strips of rats and ileum of guinea pigs induced by acetylcholine (Ach) and 5-hydroxytryptamine (5-HT) was assessed respectively. The method using nuclein and pigment methylene blue was adopted to measure the gastric retention rate of nuclein and the intestinal propulsive ratio of a nutritional semi-solid meal for assessing the effect of magnolol and honokiol (0.5, 2, 20 mg/kg) on gastric emptying and intestinal propulsion.
Magnolol and honokiol significantly inhibited the contractility of isolated gastric fundus strips of rats treated with Ach or 5-HT and isolated ileum guinea pigs treated with Ach or CaCl2, and both of them behaved as non-competitive muscarinic antagonists. Magnolol and honokiol inhibited the contraction induced by Ach in Ca2+-free medium and extracellular Ca2+-dependent contraction induced by Ach. Each group of magnolol and honokiol experiments significantly decreased the residual rate of nuclein in the stomach and increased the intestinal propulsive ratio in mice.
The inhibitory effect of magnolol and honokiol on contractility of the smooth muscles of isolated gastric fundus strips of rats and isolated ileum of guinea pigs is associated with a calcium-antagonistic effect. Magnolol and honokiol can improve the gastric emptying of a semi-solid meal and intestinal propulsive activity in mice.
研究厚朴酚与和厚朴酚对离体胃肠道平滑肌的作用及其与Ca2+的关系,以及对小鼠胃排空和肠推进活动的影响。
采用常规实验方法,利用大鼠离体胃底条和豚鼠离体回肠段测量平滑肌张力。分别评估厚朴酚10(-3)、10(-4)、10(-5)mol/L及和厚朴酚10(-4)、10(-5)、10(-6)mol/L对乙酰胆碱(Ach)和5-羟色胺(5-HT)诱导的大鼠胃底条和豚鼠回肠收缩性的影响。采用核素和色素亚甲蓝法测量核素胃潴留率及营养半固体餐的肠推进率,以评估厚朴酚与和厚朴酚(0.5、2、20mg/kg)对胃排空和肠推进的作用。
厚朴酚与和厚朴酚显著抑制用Ach或5-HT处理的大鼠离体胃底条以及用Ach或CaCl2处理的豚鼠离体回肠的收缩性,二者均表现为非竞争性毒蕈碱拮抗剂。厚朴酚与和厚朴酚抑制无Ca2+培养基中Ach诱导的收缩以及Ach诱导的细胞外Ca2+依赖性收缩。厚朴酚与和厚朴酚各实验组均显著降低小鼠胃内核素残留率并提高肠推进率。
厚朴酚与和厚朴酚对大鼠离体胃底条和豚鼠离体回肠平滑肌收缩性的抑制作用与钙拮抗作用有关。厚朴酚与和厚朴酚可改善小鼠半固体餐的胃排空和肠推进活动。