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商陆总皂苷对腹水型小鼠的抗腹水作用及机制

[Anti-ascites effect of total saponins of Phytolaccae Radix on mice with ascites and mechanism].

作者信息

Wang Cai-Xia, Yu Hong-Li, Wu Hao, Tao Xing-Bao, Xie Yu-Wei, Cheng Yan-Qiu, Zeng Ping, Wang He-Peng, Zhang Ping, Cui Xiao-Bing

机构信息

School of Pharmacy, Nanjing University of Chinese Medicine Nanjing 210023, China.

School of Pharmacy, Nanjing University of Chinese Medicine Nanjing 210023, China Jiangsu Key Laboratory of Chinese Medicine Processing Nanjing 210023, China Engineering Center of State Ministry of Education for Standardization of Chinese Medicine Processing Nanjing 210023, China.

出版信息

Zhongguo Zhong Yao Za Zhi. 2022 Aug;47(16):4411-4417. doi: 10.19540/j.cnki.cjcmm.20220211.402.

Abstract

This study investigated the anti-ascites effect of the total saponins of Phytolaccae Radix(PRTS) and the mechanism.H22 cell suspension was used(ip) to induce ascites in ICR male mice, and the model mice were randomized into model group, positive drug group(furosemide, 6 mg·kg(-1)), total extract of Phytolaccae Radix(PRTE) group, and PRTS(1.29 g·kg(-1)).Another 10 male mice were selected as the blank group.Mice in the blank group and model group were given(ig) normal saline containing 0.5% CMC-Na, and those in the positive drug group, PRTE group, and PRTS group received(ig) corresponding doses of drugs, once a day, for 8 consecutive days.The ascites volume, urine volume, and fecal water content in mice with ascites, serum levels of antidiure-tic hormone(ADH), renin in renin-angiotensin-aldosterone system(RAAS), angiotensin Ⅱ(AngⅡ), and aldosterone(ALD), expression of aquaporin(AQP)1-AQP4 in kidney, expression of AQP1, AQP3 in colon, and expression of phosphatidylinositol 3-kinase/protein kinase B(PI3 K/Akt) pathway-related proteins were detected to explore the anti-ascites mechanism of PRTS.The results showed that the PRTS can increase the urine volume and fecal water content and decrease the ascites volume of ascites mice.Moreover, PRTS significantly reduced the expression of AQP1-AQP4 in kidney and AQP1, AQP3 in colon, serum levels of renin, AngⅡ, ALD, and ADH, and the expression of p-PI3 K and p-Akt in the kidney of ascites mice.PRTS exerts anti-ascites effect by promoting urination and defecation.The mechanism is that it inhibits the activities of RAAS and ADH and suppresses the phosphorylation of PI3 K/Akt signaling pathway, thereby restricting the expression of AQPs in the kidney and colon.

摘要

本研究探讨了商陆总皂苷(PRTS)的抗腹水作用及其机制。采用H22细胞悬液腹腔注射诱导ICR雄性小鼠产生腹水,将造模小鼠随机分为模型组、阳性药物组(呋塞米,6 mg·kg⁻¹)、商陆总提取物(PRTE)组和PRTS组(1.29 g·kg⁻¹)。另选10只雄性小鼠作为空白组。空白组和模型组小鼠灌胃给予含0.5%羧甲基纤维素钠(CMC-Na)的生理盐水,阳性药物组、PRTE组和PRTS组小鼠灌胃给予相应剂量药物,每日1次,连续8天。检测腹水小鼠的腹水量、尿量和粪便含水量,血清抗利尿激素(ADH)水平、肾素-血管紧张素-醛固酮系统(RAAS)中的肾素、血管紧张素Ⅱ(AngⅡ)和醛固酮(ALD)水平,肾脏中水通道蛋白(AQP)1-AQP4的表达,结肠中AQP1、AQP3的表达以及磷脂酰肌醇3激酶/蛋白激酶B(PI3K/Akt)通路相关蛋白的表达,以探讨PRTS的抗腹水机制。结果表明,PRTS可增加腹水小鼠的尿量和粪便含水量,减少腹水量。此外,PRTS显著降低了腹水小鼠肾脏中AQP1-AQP4、结肠中AQP1和AQP3的表达,血清肾素、AngⅡ、ALD和ADH水平,以及肾脏中p-PI3K和p-Akt的表达。PRTS通过促进排尿和排便发挥抗腹水作用。其机制是抑制RAAS和ADH的活性,抑制PI3K/Akt信号通路的磷酸化,从而限制肾脏和结肠中AQPs的表达。

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