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阐明同型半胱氨酸增强S-腺苷同型半胱氨酸水解酶抑制剂9-(反式-2',反式-3'-二羟基环戊-4'-烯基)-腺嘌呤抗痘苗病毒作用的机制。

Elucidation of the mechanism by which homocysteine potentiates the anti-vaccinia virus effects of the S-adenosylhomocysteine hydrolase inhibitor 9-(trans-2',trans-3'-dihydroxycyclopent-4'-enyl)-adenine.

作者信息

Hasobe M, McKee J G, Ishii H, Cools M, Borchardt R T, De Clercq E

机构信息

Department of Pharmaceutical Chemistry, University of Kansas, Lawrence 66045.

出版信息

Mol Pharmacol. 1989 Sep;36(3):490-6.

PMID:2779528
Abstract

9-(trans-2',trans-3'-dihydroxycyclopent-4'-enyl)-adenine (DHC), a specific inhibitor of S-adenosyl-L-homocysteine (AdoHcy) hydrolase, has been used in this study to elucidate the mechanism by which DL-homocysteine (Hcy) potentiates the antiviral effects of AdoHcy hydrolase inhibitors as reported by De Clercq [Biochem. Pharmacol. 36:2567-2575 (1987)]. The potentiating effects of Hcy on the antiviral effects of DHCA were determined using murine L929 cells infected with vaccinia virus. When virus-infected cells were incubated with DHCA alone or in combination with various concentrations of Hcy, the following IC50 values (concentrations of the drug required to reduce by 50% viral plaque formation) were observed: 0.30 microM (0 mM Hcy), 0.15 microM (0.3 mM Hcy), 0.09 microM (1.0 mM Hcy), and 0.04 microM (3.0 mM Hcy). In the drug combination studies, increased cellular toxicity, compared with DHCA alone, was observed only at the highest concentration of Hcy (3.0 mM); thus, at lower concentrations Hcy increased the antiviral effectiveness [ID50 (concentration of the drug required to reduce the increase in cell number by 50%)/IC50] of DHCA. For example the following ID50/IC50 values were observed for DHCA alone or in combination with Hcy: 64 (0 mM Hcy), 113 (0.3 mM Hcy), 151 (1.0 mM Hcy), and 88 (3.0 mM Hcy). In these studies, Hcy was also observed to potentiate the increase in cellular levels of AdoHcy and the ratio of AdoHcy/S-adenosyl-L-methionine (AdoMet) in DHCA-treated cells. In earlier studies, our laboratory has shown that antiviral effects of DHCA are caused by only slight elevations in intracellular levels of AdoHcy [from 50 pmol/mg of protein (controls) to 100-200 pmol/mg of protein (drug-treated)] and slight elevations in the ratios of AdoHcy/AdoMet [from 0.05-0.1 (control) to 0.15-0.20 (drug-treated)]. Thus, in the presence of Hcy, lower concentrations of DHCA are needed to increase the intracellular concentration of AdoHcy and the AdoHcy/AdoMet ratio to levels that suppress replication of vaccinia virus. Murine L929 cells were shown to contain DHCA-sensitive and DHCA-insensitive forms of AdoHcy hydrolase. Based on the results of labeling experiments using [2,8-3H]adenosine and [35S]methionine, the elevated levels of AdoHcy were shown to arise from the reaction of [2,8-3H]adenosine and Hcy, catalyzed by the DHCA-insensitive form of AdoHcy hydrolase.

摘要

9-(反式-2',反式-3'-二羟基环戊-4'-烯基)-腺嘌呤(DHC)是S-腺苷-L-高半胱氨酸(AdoHcy)水解酶的特异性抑制剂,本研究中使用它来阐明如De Clercq所报道的[《生物化学与药物学》36:2567 - 2575(1987)]DL-高半胱氨酸(Hcy)增强AdoHcy水解酶抑制剂抗病毒作用的机制。使用感染痘苗病毒的小鼠L929细胞测定Hcy对DHCA抗病毒作用的增强效果。当病毒感染细胞单独与DHCA孵育或与不同浓度的Hcy联合孵育时,观察到以下半数抑制浓度(IC50,即使病毒空斑形成减少50%所需的药物浓度)值:0.30微摩尔/升(0毫摩尔/升Hcy)、0.15微摩尔/升(0.3毫摩尔/升Hcy)、0.09微摩尔/升(1.0毫摩尔/升Hcy)和0.04微摩尔/升(3.0毫摩尔/升Hcy)。在药物联合研究中,仅在最高浓度的Hcy(3.0毫摩尔/升)时观察到与单独使用DHCA相比细胞毒性增加;因此,在较低浓度时Hcy增加了DHCA的抗病毒效力[半数抑制剂量(ID50,即使细胞数量增加减少50%所需的药物浓度)/IC50]。例如,单独使用DHCA或与Hcy联合使用时观察到以下ID50/IC50值:64(0毫摩尔/升Hcy)、113(0.3毫摩尔/升Hcy)、151(1.0毫摩尔/升Hcy)和88(3.0毫摩尔/升Hcy)。在这些研究中,还观察到Hcy增强了DHCA处理细胞中AdoHcy细胞水平的升高以及AdoHcy/S-腺苷-L-甲硫氨酸(AdoMet)的比值。在早期研究中,我们实验室已表明DHCA的抗病毒作用仅由细胞内AdoHcy水平的轻微升高[从50皮摩尔/毫克蛋白质(对照)升至100 - 200皮摩尔/毫克蛋白质(药物处理)]以及AdoHcy/AdoMet比值的轻微升高[从0.05 - 0.1(对照)升至0.15 - 0.20(药物处理)]引起。因此,在有Hcy存在的情况下,需要较低浓度的DHCA来将细胞内AdoHcy浓度和AdoHcy/AdoMet比值提高到抑制痘苗病毒复制的水平。已表明小鼠L929细胞含有对DHCA敏感和不敏感的AdoHcy水解酶形式。基于使用[2,8 - 3H]腺苷和[35S]甲硫氨酸的标记实验结果,AdoHcy水平的升高显示是由AdoHcy水解酶的DHCA不敏感形式催化的[2,8 - 3H]腺苷与Hcy的反应引起的。

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