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9-β-D-阿拉伯呋喃糖基次黄嘌呤5'-单磷酸酯对病毒性角膜炎的抑制作用

Viral keratitis-inhibitory effect of 9-beta-D-arabinofuranosylhypoxanthine 5'-monophosphate.

作者信息

Sidwell R W, Allen L B, Huffman J H, Revankar G R, Robins R K, Tolman R L

出版信息

Antimicrob Agents Chemother. 1975 Oct;8(4):463-7. doi: 10.1128/AAC.8.4.463.

DOI:10.1128/AAC.8.4.463
PMID:1190753
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC429372/
Abstract

Topical application of 9-beta-d-arabinofuranosylhypoxanthine 5'-monophosphate (ara-HxMP) significantly inhibited the development of keratitis induced by types 1 and 2 herpes simplex virus and vaccinia virus in the eyes of rabbits. Parameters for evaluation of efficacy were infectivity (corneal opacity, lesion size, and type), Draize (erythema, conjunctival swelling, and discharge), and reduction in titer of recoverable virus from the eye. When the relative efficacy of the related compounds 9-beta-d-arabinofuranosyladenine (ara-A), ara-A 5'-monophosphate (ara-AMP), and ara-Hx was determined against type 1 herpes simplex virus in a parallel experiment, the more water-soluble compounds (ara-HxMP, ara-AMP) were the most effective. The relative efficacy of ara-A was also determined against type 2 herpes and vaccinia virus-induced keratitis. Mortality in rabbits due to central nervous system involvement caused by types 1 and 2 herpes simplex virus was inhibited. Ara-HxMP was not discernibly toxic to the eye at concentrations of at least 20%; efficacy was still discernible with a 0.1% solution.

摘要

9-β-D-阿拉伯呋喃糖基次黄嘌呤5'-单磷酸酯(ara-HxMP)的局部应用显著抑制了1型和2型单纯疱疹病毒以及痘苗病毒诱导的家兔角膜炎的发展。评估疗效的参数包括感染性(角膜混浊、病变大小和类型)、德雷兹(红斑、结膜肿胀和分泌物)以及眼内可回收病毒滴度的降低。在一项平行实验中,当测定相关化合物9-β-D-阿拉伯呋喃糖基腺嘌呤(ara-A)、ara-A 5'-单磷酸酯(ara-AMP)和ara-Hx对1型单纯疱疹病毒的相对疗效时,水溶性更高的化合物(ara-HxMP、ara-AMP)最为有效。还测定了ara-A对2型单纯疱疹和痘苗病毒诱导的角膜炎的相对疗效。1型和2型单纯疱疹病毒引起的中枢神经系统受累导致的家兔死亡率受到抑制。在至少20%的浓度下,ara-HxMP对眼睛没有明显毒性;0.1%的溶液仍可观察到疗效。

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Viral keratitis-inhibitory effect of 9-beta-D-arabinofuranosylhypoxanthine 5'-monophosphate.9-β-D-阿拉伯呋喃糖基次黄嘌呤5'-单磷酸酯对病毒性角膜炎的抑制作用
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Antimicrob Agents Chemother. 1976 Dec;10(6):885-8. doi: 10.1128/AAC.10.6.885.

本文引用的文献

1
Use of 5-iodo-2'-deoxyuridine (IDU) in treatment of herpes simplex keratitis.5-碘-2'-脱氧尿苷(IDU)在单纯疱疹性角膜炎治疗中的应用。
Arch Ophthalmol. 1962 Aug;68:235-9. doi: 10.1001/archopht.1962.00960030239015.
2
Herpes simplex treatment with IDU and corticosteroids.用碘苷和皮质类固醇治疗单纯疱疹。
Arch Ophthalmol. 1963 Apr;69:468-72. doi: 10.1001/archopht.1963.00960040474008.
3
Azapurine nucleosides. 2. Synthesis and antiviral activity of 7-amino-3- -D-arabinofuranosyl-v-triazolo (4,5-d)pyrimidine and related nucleosides.氮杂嘌呤核苷。2. 7-氨基-3-β-D-阿拉伯呋喃糖基-1,2,4-三唑并[4,5-d]嘧啶及相关核苷的合成与抗病毒活性。
J Med Chem. 1972 Sep;15(9):883-7. doi: 10.1021/jm00279a002.
4
The chemotherapy of herpes iritis with adenine arabinoside and cytarabine.
Arch Ophthalmol. 1970 Dec;84(6):783-7. doi: 10.1001/archopht.1970.00990040785018.
5
The management of ocular herpes.眼部疱疹的管理
Trans Ophthalmol Soc U K (1962). 1967;87:59-84.
6
Effect of 1-beta-D-ribofuranosyl1-1,2,4-triazole-3-carboxamide (virazole, ICN 1229) on herpes and vaccinia keratitis and encephalitis in laboratory animals.1-β-D-呋喃核糖基-1,2,4-三唑-3-甲酰胺(病毒唑,ICN 1229)对实验动物疱疹性和牛痘性角膜炎及脑炎的作用
Antimicrob Agents Chemother. 1973 Feb;3(2):242-6. doi: 10.1128/AAC.3.2.242.
7
Prophylaxis and therapy of experimental ocular herpes simplex. Comparison of idoxuridine, adenine arabinoside, and hypoxanthine arabinoside.实验性眼部单纯疱疹的预防与治疗。碘苷、阿糖腺苷和阿糖次黄嘌呤的比较。
Arch Ophthalmol. 1974 Nov;92(5):417-21. doi: 10.1001/archopht.1974.01010010429012.
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Anti-DNA virus activity of the 5'-nucleotide and 3',5'-cyclic nucleotide of 9-beta-D-arabinofuranosyladenine.9-β-D-阿拉伯呋喃糖基腺嘌呤的5'-核苷酸和3',5'-环核苷酸的抗DNA病毒活性
Chemotherapy. 1973;19(6):325-40. doi: 10.1159/000221473.
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Effect of adenine arabinoside on severe Herpesvirus hominis infections in man.阿糖腺苷对人类严重单纯疱疹病毒感染的作用。
J Infect Dis. 1973 Nov;128(5):658-63. doi: 10.1093/infdis/128.5.658.
10
Synthesis and anti-deoxyribonucleic acid virus activity of certain 9-beta-D-arabinofuranosyl-2-substituted adenine derivatives.某些9-β-D-阿拉伯呋喃糖基-2-取代腺嘌呤衍生物的合成及其抗脱氧核糖核酸病毒活性
J Med Chem. 1974 Feb;17(2):242-4. doi: 10.1021/jm00248a023.