β-石竹烯脂质体对乙二醇所致大鼠尿石症的体内外疗效

Ranjith Kumar R , Suresh Janadri , Manjunatha PM , Madhu M V , Rakshitha K B , Preeti P Angadi , Uday Raj Sharma , Surrendra Vada , Nageena Taj , Jyotsna S Kharvi
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引用次数: 0

摘要

背景:尿石症是指泌尿系统结石的形成。β-石竹烯,一种双环倍半萜,存在于丁香(Dīng z′Xiāng)、肉桂(Ròu Guì)、黑胡椒(Hú Jiāo)和人参(r n Shēn)等草药中。尽管具有潜力,β-石竹烯的抗尿石活性,特别是在脂质体制剂中,仍未被探索。本研究旨在评价β-石竹烯脂质体对乙二醇致Wistar白化大鼠尿石症的抗尿石作用,并探讨其机制。材料,方法体外:采用聚集法、成核法、滴定法等多种体外实验方法,研究了草酸钙(Caox)和草酸钠溶液对β-载茶烯脂质体的百分比抑制作用,以评估其抗尿石作用。体内实验:以乙二醇为诱导剂。将白化大鼠分为6组。第一组为正常饮食。II-VI组以0.75% v/v的水掺入EG治疗肾结石,III- v组分别以100 mg/kg、200 mg/kg、400 mg/kg的β-载茶烯脂质体治疗。vi组给予标准药物半胱氨酸(750 mg/kg)。结果体外和体内模型均证实脂质体β-石竹烯(BCP)显著抑制草酸钙晶体的形成、聚集和溶解。BCP显著降低血清和尿液肾功能障碍和氧化应激标志物,最高剂量(400 mg/kg)显示出与标准药物(胱氨酸)相似的效果。结论β-石竹烯(BCP)脂质体对尿石症有较好的治疗效果,能有效防止结石形成,改善肾功能。它显示出与标准治疗相当的疗效,这表明它有可能成为治疗尿石症的可行替代或补充疗法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
In-vitro & in-vivo efficacy of liposomal β-carryophyllene in ethylene glycol induced urolithiasis in rats

Background

Urolithiasis refers to the formation of stones in the urinary system. β-Caryophyllene, a bicyclic sesquiterpene found in herbs like cloves (Dīng Zǐ Xiāng), cinnamon (Ròu Guì), Black Pepper (Hú Jiāo) and Ginseng (Rén Shēn). Despite its potential, the antiurolithiatic activity of β-Caryophyllene, particularly in liposomal formulations, remains unexplored. This study aimed to evaluate the antiurolithiatic effects of liposomal β-Caryophyllene in ethylene glycol-induced urolithiasis in Wistar albino rats and elucidate its underlying mechanisms.

Materials & methods

IN-VITRO: Using various in-vitro methods like aggregation, nucleation and titrimetric assay the percentage inhibition of calcium oxalate using the calcium chloride (Caox) and sodium oxalate solutions against the liposomal β-carryophyllene was performed for assessing anti-urolithiatic effect.
IN-VIVO: Ethylene glycol was used as the inducing agent. Albino rats were separated into 6 groups. Group-I named as normal diet. Group II-VI was given 0.75 % v/v EG was mixed in drinking water for causing renal stones, along with group III- V was treated with liposomal β-carryophyllene 100 mg/kg, 200 mg/kg and 400 mg/kg respectively. Group-VI was treated with standard drug, cystone (750 mg/kg).

Results

The study proved that liposomal β-caryophyllene (BCP) significantly inhibits calcium oxalate crystal formation, aggregation, and dissolution in both in-vitro and in-vivo models. BCP significantly reduced serum and urine markers of renal dysfunction and oxidative stress, with the highest dose (400 mg/kg) demonstrating effects similar to the standard drug (cystone).

Conclusion

Liposomal β-caryophyllene (BCP) shows promising therapeutic agent for urolithiasis, effectively preventing crystal formation and improving renal function. It demonstrated comparable efficacy to the standard treatment, suggesting its potential as a viable alternative or complementary therapy for managing urolithiasis.
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