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抗氧化愈合制剂在实验性皮肤和生殖器单纯疱疹病毒感染局部治疗中的评估

Evaluation of antioxidant healing formulations in topical therapy of experimental cutaneous and genital herpes simplex virus infections.

作者信息

Sheridan J, Kern E, Martin A, Booth A

机构信息

Ohio State University Health Sciences Center, Columbus 43210-1241, USA.

出版信息

Antiviral Res. 1997 Dec;36(3):157-66. doi: 10.1016/s0166-3542(97)00049-1.

Abstract

A genital HSV-2 infection of guinea pigs and a cutaneous HSV-1 infection in mice were used to examine the ability of antioxidant components CRT1 to reduce lesion development, duration, and severity. CRT is a patented antioxidant formulation developed by Warner-Lambert Worldwide Consumer Healthcare R. and D. CRT contains three components that work synergistically: vitamin E, sodium pyruvate and membrane stabilizing fatty acids. The MS strain of HSV-2 was utilized for intravaginal inoculation of guinea pigs with approximately 1.2 x 10(5) plaque forming units. The guinea pigs were treated on the external genital skin four times daily for 10 days beginning 48 h post viral inoculation. This study was designed to optimize the CRT formulations that would be used to quantify the synergistic effect of the CRT components. SKH-1 male hairless mice were inoculated with 1 x 10(7) HSV-1 (McIntyre strain) on the dorsal surface of the mouse and treated with CRT formulations starting on the afternoon of the day of infection, and treated for the following 14 days. In the guinea pig model, the CRT formula that contained all three CRT components, worked synergistically to reduce lesion development, duration and severity scores significantly compared to vehicle control or acyclovir. Acyclovir was the only compound that reduced viral titers, but in contrast to CRT, acyclovir did not reduce lesion development, duration or severity. The quantitative effect of the three CRT components was demonstrated in the mouse model.

摘要

采用豚鼠生殖器单纯疱疹病毒2型(HSV - 2)感染模型和小鼠皮肤单纯疱疹病毒1型(HSV - 1)感染模型,研究抗氧化剂CRT1减轻损伤发生、持续时间及严重程度的能力。CRT是由华纳 - 兰伯特全球消费者保健研发部开发的一种专利抗氧化剂配方。CRT含有三种协同发挥作用的成分:维生素E、丙酮酸钠和膜稳定脂肪酸。HSV - 2的MS毒株用于给豚鼠阴道内接种约1.2×10⁵ 蚀斑形成单位。在病毒接种后48小时开始,对豚鼠外生殖器皮肤每天进行4次治疗,持续10天。本研究旨在优化用于量化CRT各成分协同作用的CRT配方。给SKH - 1雄性无毛小鼠背部接种1×10⁷ HSV - 1(麦金太尔毒株),从感染当天下午开始用CRT配方进行治疗,并持续治疗14天。在豚鼠模型中,与赋形剂对照或阿昔洛韦相比,含有CRT所有三种成分的CRT配方协同作用,显著减轻了损伤的发生、持续时间和严重程度评分。阿昔洛韦是唯一能降低病毒滴度的化合物,但与CRT不同的是,阿昔洛韦并未减轻损伤的发生、持续时间或严重程度。在小鼠模型中证实了CRT三种成分的定量作用。

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