Thomas T J, Seibold J R, Adams L E, Hess E V
Department of Medicine, University of Medicine and Dentistry of New Jersey-Robert Wood Johnson Medical School, New Brunswick 08903, USA.
Biochem J. 1995 Oct 1;311 ( Pt 1)(Pt 1):183-8. doi: 10.1042/bj3110183.
Hydralazine is an antihypertensive drug that elicits andti-nuclear antibodies in patients as an adverse effect. We investigated the ability of hydralazine to promote/stabilize the triplex DNA form of poly(dA).2poly(dT). Under conditions of low ionic strength, the polynucleotide melted as a double helix with a melting temperature (Tm) of 55.3 degrees C. Hydralazine destabilized this duplex form by reducing its Tm to 52.5 degrees C. Spermidine (2.5 microM), a natural polyamine, provoked the triplex form of poly(dA)-.2poly(dT) with two melting transitions, Tm1 of 42.8 degrees C corresponding to triplex-->duplex+single-stranded DNA and Tm2 of 65.4 degrees C, corresponding to duplex melting. Triplex DNA thus formed in the presence of spermidine was further stabilized by hydralazine (250 microM) with a Tm1 of 53.6 degrees C. A similar stabilization effect of hydralazine was found on triplex DNA formed in the presence of 5 mM Mg2+. CD spectra revealed conformational perturbations of DNA in the presence of spermidine and hydralazine. These results support the hypothesis that hydralazine is capable of stabilizing unusual forms of DNA. In contrast with the weak immunogenicity of DNA in its right-handed B-DNA conformation, these unusual forms are immunogenic and have the potential to elicit anti-DNA antibodies. To test this possibility, we analysed sera from a panel of 25 hydralazine-treated patients for anti-(triplex DNA) antibodies using an ELISA. Our results showed that 72% of sera from hydralazine-treated patients contained antibodies reacting toward the triplex DNA. In contrast, there was no significant binding of normal human sera to triplex DNA. Taken together our data indicate that hydralazine and related drugs might exert their action by interacting with DNA and stabilizing higher-order structures such as the triplex DNA.
肼屈嗪是一种降压药,可在患者体内引发抗核抗体,这是一种不良反应。我们研究了肼屈嗪促进/稳定聚(dA)·2聚(dT)三链DNA形式的能力。在低离子强度条件下,多核苷酸以双链螺旋形式解链,解链温度(Tm)为55.3℃。肼屈嗪通过将其Tm降低至52.5℃使这种双链形式不稳定。亚精胺(2.5 microM),一种天然多胺,引发了聚(dA)·2聚(dT)的三链形式,有两个解链转变,Tm1为42.8℃,对应三链→双链+单链DNA,Tm2为65.4℃,对应双链解链。在亚精胺存在下如此形成的三链DNA通过肼屈嗪(250 microM)进一步稳定,Tm1为53.6℃。在5 mM Mg2+存在下形成的三链DNA上也发现了肼屈嗪类似的稳定作用。圆二色光谱揭示了在亚精胺和肼屈嗪存在下DNA的构象扰动。这些结果支持了肼屈嗪能够稳定异常形式DNA的假说。与右手B-DNA构象的DNA的弱免疫原性相反,这些异常形式具有免疫原性,并且有可能引发抗DNA抗体。为了测试这种可能性,我们使用酶联免疫吸附测定法分析了一组25名接受肼屈嗪治疗患者的血清中的抗(三链DNA)抗体。我们的结果表明,接受肼屈嗪治疗患者的血清中有72%含有与三链DNA反应的抗体。相比之下,正常人血清与三链DNA没有明显的结合。综合我们的数据表明,肼屈嗪及相关药物可能通过与DNA相互作用并稳定如三链DNA等高级结构来发挥其作用。