Department of Pharmacology II, School of Pharmacy and Pharmaceutical Sciences, Mukogawa Women's University.
Center for Pharma-Food Research (CPFR), Graduate School of Pharmaceutical Sciences, University of Shizuoka.
Biol Pharm Bull. 2020;43(5):817-822. doi: 10.1248/bpb.b19-01027.
Diarrhea is often caused by changes in lifestyle, stress, or side effects of drugs. Acanthopanax senticosus root extract (ASRE) has long been used as a functional food remedy with anti-fatigue, neuroprotective, and immunomodulatory activities. However, it is unclear whether ASRE has beneficial effects on gastrointestinal (GI) motility. Therefore, we first investigated whether ASRE directly affects contractile functions of the isolated mouse ileum, and then assessed its effects on GI transit of a charcoal meal in normal mice and a carbachol (CCh)-induced diarrhea mouse model. ASRE caused contraction of the isolated mouse ileum and the maximum contraction was approximately half of that induced by acetylcholine (ACh) administration. In the presence of atropine, this ASRE-induced contraction disappeared, while relaxation responses were observed. However, ASRE reduced potassium chloride- and ACh-induced contractions, and the inhibitory effect was not counteracted by a β-blocker. Administration of a nitric oxide synthase inhibitor or potassium channel blockers did not affect the ASRE-induced relaxation. Oral administration of ASRE for 1 and 4 d reduced the increased GI transit in CCh-treated but did not affect the GI transit of normal mice. These results indicate that ASRE exhibited dual effects of contraction via muscarinic receptors and direct relaxation on mouse ileal function, and its relaxant effect could be useful in treating diarrhea symptoms, resulting in an increase in the parasympathetic nerve activities.
腹泻通常是由生活方式改变、压力或药物副作用引起的。刺五加根提取物(ASRE)长期以来一直被用作具有抗疲劳、神经保护和免疫调节作用的功能性食品补救剂。然而,目前尚不清楚 ASRE 是否对胃肠道(GI)蠕动有有益影响。因此,我们首先研究了 ASRE 是否直接影响分离的小鼠回肠的收缩功能,然后评估了其对正常小鼠和毛果芸香碱(CCh)诱导的腹泻小鼠模型中炭餐 GI 转运的影响。ASRE 引起分离的小鼠回肠收缩,最大收缩约为乙酰胆碱(ACh)给药诱导的收缩的一半。在阿托品存在下,这种 ASRE 诱导的收缩消失,而观察到松弛反应。然而,ASRE 减少了氯化钾和 ACh 诱导的收缩,并且抑制作用不受β受体阻滞剂拮抗。一氧化氮合酶抑制剂或钾通道阻滞剂的给药均未影响 ASRE 诱导的松弛。ASRE 的口服给药 1 和 4 天可减少 CCh 处理后增加的 GI 转运,但不影响正常小鼠的 GI 转运。这些结果表明,ASRE 对小鼠回肠功能表现出通过毒蕈碱受体收缩和直接松弛的双重作用,其松弛作用可用于治疗腹泻症状,导致副交感神经活动增加。