畜牧与饲料科学 ›› 2025, Vol. 46 ›› Issue (3): 17-23.doi: 10.12160/j.issn.1672-5190.2025.03.003

• 基础研究 • 上一篇    下一篇

罗布麻水提物对小鼠胃肠运动的抑制作用研究

赵昕, 贺元萧, 李杨, 热则古丽·艾科拜尔, 赵红琼   

  1. 新疆农业大学动物医学学院,新疆 乌鲁木齐 830052
  • 收稿日期:2025-04-01 出版日期:2025-05-30 发布日期:2025-09-02
  • 通讯作者: 赵红琼(1974—),女,教授,主要研究方向为生物活性物质结构与功能。
  • 作者简介:赵昕(2004—),女,所学专业为动植物检疫。
  • 基金资助:
    新疆农业大学大学生创新项目(dxscx2024440)

Study on the Inhibitory Effect of Aqueous Extract from Apocynum venetum on Gastrointestinal Motility in Mice

ZHAO Xin, HE Yuanxiao, LI Yang, REZEGULI·Aikebaier, ZHAO Hongqiong   

  1. College of Veterinary Medicine, Xinjiang Agricultural University, Urumqi, 830052, China
  • Received:2025-04-01 Online:2025-05-30 Published:2025-09-02

摘要: [目的]探究罗布麻水提物对小鼠胃肠运动的影响,为罗布麻产品的科学使用提供参考。[方法]用罗布麻水提物进行2倍浓度递增试验、一次性浓度试验及与毒蕈碱型受体(M-受体)激动剂联合用药试验,探究其对小鼠离体小肠段运动的影响;给小鼠灌胃5、25、125 g/L罗布麻水提物或生理盐水,然后再灌胃墨汁,计算肠推进率和均分4段长度小肠的墨汁残留率。[结果]与用药前比较,2倍浓度递增(0.5~8.0 g/L)的罗布麻水提物可降低离体小肠段的收缩张力和收缩幅度;一次性浓度(4.0 g/L)罗布麻水提物给药后极显著(P<0.01)降低肠段收缩张力和收缩幅度,分别为用药前的(74.5±2.2)%和(82.0±2.6)%;罗布麻水提物与M-受体激动剂氯贝胆碱(BCh)联合用药后离体小肠段收缩峰值与用药前峰值百分比[(180.8±6.4)%]极显著(P<0.01)高于台氏液与BCh联合用药[(158.1±4.7)%]。罗布麻水提物灌胃小鼠剂量依赖性降低小鼠肠推进率,且墨汁主要残留在小肠的第3段。[结论]罗布麻水提物对小鼠胃肠运动具有抑制作用,其对小肠运动的抑制作用可能与抑制M-受体无关。

关键词: 罗布麻, 小鼠, 小肠, 肠推进率, M-受体

Abstract: [Objective] To investigate the effects of Apocynum venetum water extract (AVWE) on gastrointestinal motility in mice and provide a scientific reference for the rational use of Apocynum venetum-based products. [Methods] A two-fold increasing concentration test, single-concentration test, and combined administration with a muscarinic receptor (M-receptor) agonist were conducted to evaluate the effects of AVWE on isolated small intestinal segments in mice. Mice were intragastrically administered 5, 25, 125 g/L AVWE or saline, followed by ink suspension, to calculate intestinal propulsion rates and ink retention rates in four equally divided segments of the small intestine. [Results] Compared with pre-treatment values, two-fold increasing concentrations of AVWE (0.5-8.0 g/L) could reduce the contractile tension and amplitude of isolated intestine. A single concentration of AVWE (4.0 g/L) highly significantly (P<0.01) decreased contractile tension and amplitude to (74.5±2.2)% and (82.0±2.6)% of pre-treatment levels, respectively. The peak contraction percentage of intestine treated with AVWE combined with the M-receptor agonist bethanechol chloride (BCh) [(180.8±6.4)%] was extremely significantly (P<0.01) higher than that with Tyrode’s solution combined with BCh [(158.1±4.7)%]. AVWE administration dose-dependently reduced intestinal propulsion rate, with ink predominantly retained in the third part of the small intestine. [Conclusion] AVWE inhibits gastrointestinal motility in mice, and its suppressive effect on intestinal motility may be independent of M-receptor antagonism.

Key words: Apocynum venetum, mice, small intestine, intestinal propulsion rate, M-receptor

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