骆驼奶蛋白水解物可缓解高果糖喂养大鼠的肝脏脂肪变性和高血压。

IF 3.9 3区 医学 Q1 MEDICAL LABORATORY TECHNOLOGY
Mohammad A Alshuniaber, Ghedeir M Alshammari, Samy M Eleawa, Abu ElGasim A Yagoub, Abdullrahman S Al-Khalifah, Maha H Alhussain, Laila Naif Al-Harbi, Mohammed Abdo Yahya
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引用次数: 0

摘要

背景:骆驼奶在传统医学中被用于治疗糖尿病、高血压和其他代谢性疾病:本研究评估了驼奶蛋白水解物(CMH)对高果糖(HF)喂养大鼠的抗脂肪肝和降血压作用,并将其与完整驼奶蛋白提取物(ICM)的作用进行了比较:将成年雄性 Wistar 大鼠分为 6 组(每组 8 只):1)对照组;2)ICM(1000 毫克/千克)组;3)CMH(1000 毫克/千克)组;4)HF(15% 饮用水)组;5)HF(15%)+ ICM(1000 毫克/千克)组;6)HF(15%)+ CMH(1000 毫克/千克)组。所有治疗均每日口服,连续 21 周:结果:ICM 和 CMH 均可降低高频饲养大鼠的空腹血糖和胰岛素水平、血清和肝脏胆固醇和甘油三酯水平、血清谷丙转氨酶和谷草转氨酶、血管紧张素 II、血管紧张素转换酶、内皮素-1 和尿酸水平。此外,ICM 和 CMH 还能减少肝细胞中的肝脂肪沉积,减轻肝细胞损伤。这与肝脏 AMPK 活性增加、PPARα mRNA 增加、果糖激酶 C、SREBP1、SREBP2、脂肪酸合成酶和 HMG-CoA 还原酶表达减少有关。两种治疗方法都能降低收缩压和舒张压。然而,与 ICM 相比,CMH 对所有这些参数的影响更大:本研究结果鼓励在大规模人群和临床研究中使用 CMH 治疗代谢性脂肪变性和高血压。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Camel milk protein hydrosylate alleviates hepatic steatosis and hypertension in high fructose-fed rats.

Camel milk protein hydrosylate alleviates hepatic steatosis and hypertension in high fructose-fed rats.

Camel milk protein hydrosylate alleviates hepatic steatosis and hypertension in high fructose-fed rats.

Camel milk protein hydrosylate alleviates hepatic steatosis and hypertension in high fructose-fed rats.

Context: Camel milk is used in traditional medicine to treat diabetes mellitus hypertension and other metabolic disorders.

Objective: This study evaluated the antisteatotic and antihypertensive effects of camel milk protein hydrolysate (CMH) in high fructose (HF)-fed rats and compared it with the effects afforded by the intact camel milk protein extract (ICM).

Materials and methods: Adult male Wistar rats were divided into 6 groups (n = 8 each) as 1) control, 2) ICM (1000 mg/kg), 3) CMH (1000 mg/kg), 4) HF (15% in drinking water), 5) HF (15%) + ICM (1000 mg/kg), and 6) HF (15%) + CMH (1000 mg/kg). All treatments were given orally for 21 weeks, daily.

Results: Both ICM and CMH reduced fasting glucose and insulin levels, serum and hepatic levels of cholesterol and triglycerides, and serum levels of ALT and AST, angiotensin II, ACE, endothelin-1, and uric acid in HF-fed rats. In addition, both ICM and CMH reduced hepatic fat deposition in the hepatocytes and reduced hepatocyte damage. This was associated with an increase in the hepatic activity of AMPK, higher PPARα mRNA, reduced expression of fructokinase C, SREBP1, SREBP2, fatty acid synthase, and HMG-CoA-reductase. Both treatments lowered systolic and diastolic blood pressure. However, the effects of CMH on all these parameters were greater as compared to ICM.

Discussion and conclusions: The findings of this study encourage the use of CMH in a large-scale population and clinical studies to treat metabolic steatosis and hypertension.

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来源期刊
Pharmaceutical Biology
Pharmaceutical Biology 医学-药学
CiteScore
6.70
自引率
2.60%
发文量
191
审稿时长
1 months
期刊介绍: Pharmaceutical Biology will publish manuscripts describing the discovery, methods for discovery, description, analysis characterization, and production/isolation (including sources and surveys) of biologically-active chemicals or other substances, drugs, pharmaceutical products, or preparations utilized in systems of traditional medicine. Topics may generally encompass any facet of natural product research related to pharmaceutical biology. Papers dealing with agents or topics related to natural product drugs are also appropriate (e.g., semi-synthetic derivatives). Manuscripts will be published as reviews, perspectives, regular research articles, and short communications. The primary criteria for acceptance and publication are scientific rigor and potential to advance the field.
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