希尔凡草药软膏对人类皮肤利什曼病的治疗效果与葡甘定的比较

IF 0.7 Q4 MEDICINE, RESEARCH & EXPERIMENTAL
Advanced biomedical research Pub Date : 2024-08-26 eCollection Date: 2024-01-01 DOI:10.4103/abr.abr_243_23
Maryam Aghaei, Shahrzad Aghaei, Ali Ghelichzadeh, Nazli Ansari, Mahdi Fakhar, Sayed Mohsen Hosseini, Zabihollah Shahmoradi, Seyed Hossein Hejazi
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引用次数: 0

摘要

背景:皮肤利什曼病(CL)是由大头利什曼病(L. major)寄生虫引起的,全世界每年有 150 万到 200 万人感染该病。虽然疫苗和抗寄生虫药物的研究取得了一定的成功,但其不良反应包括毒性大、再生时间长和瘢痕形成。这凸显了研究替代具有抗菌和抗氧化特性的天然产品(如植物提取物和植物油)的重要性。由于希尔凡草药软膏中的每种成分(芦荟、布拉泽贝尔、黑升麻、蜂胶、薰衣草和橄榄油)的抗利什曼病效果都已分别得到研究和证实,因此似乎这些成分的组合在治疗 CL 方面的抗利什曼病效果会越来越好。因此,本研究调查了希尔凡草药软膏对伊朗利什曼病患者的治疗效果,并将其与葡糖酸(麦格鲁明)进行了比较:将 60 名利什曼病患者分为对照组和试验组。对照组和试验组分别接受鞘内注射葡萄糖醛酸和希尔凡草药乳膏(每日两次):对照组皮损面积平均为(51.5±32.5)平方米,治疗后为11.11±16.28平方米;试验组皮损面积平均为(50.8±31.2)平方米,治疗后为0.0±0.0平方米。此外,对照组和试验组的平均治疗时间分别为(43.9±14.4)天和(30.5±7.4)天。两组治疗后的病灶大小有明显差异:数据表明,Shirvan 草药软膏可作为治疗人类 CL 的替代药物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Therapeutic Effect of Shirvan Herbal Ointment on Human Cutaneous Leishmaniasis Compared with Glucantime.

Background: Cutaneous leishmaniasis (CL) infection is caused by the Leishmania major (L. major) parasite and affects 1.5 to 2 million people worldwide each year. Although research into vaccines and antiparasitic drugs has been somewhat successful, their adverse effects include high toxicity, prolonged regeneration, and scarring. This has highlighted the importance of research to replace natural products with antibacterial and antioxidant properties, such as vegetable extracts and oils. Since, the anti-leishmaniasis effect of each of the components of Shirvan herbal ointment (aloe vera, Brazembel, Nigella sativa, propolis, lavender, and olive oil) has been separately studied and confirmed, it seems that the combination of these components can have an increasing anti-leishmanial effect to treat CL. Therefore, this study investigated the therapeutic impact of Shirvan herbal ointment on Iranian patients with leishmaniasis in comparison with glucantime (meglumine).

Materials and methods: Sixty patients with leishmaniasis were divided into the control and test groups. The control and test groups received intralesional glucantime and Shirvan herbal cream (two times daily), respectively.

Results: The size mean of the lesion was 51.5 ± 32.5 before and 11.11 ± 16.28 after treatment in the control group and 50.8 ± 31.2 before and 0.0 ± 0.0 after treatment in the test group. In addition, the period mean of treatment was 43.9 ± 14.4 days and 30.5 ± 7.4 days in the control and test groups, respectively. There was a significant difference in lesion size between the two groups after treatment.

Conclusion: Data suggested that Shirvan herbal ointment can be an alternative drug in the treatment of human CL.

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