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宫颈黏液的变化可阻止精子穿透。

Changes in cervical mucus that prevent penetration by spermatozoa.

作者信息

Chantler E, Sharma R, Sharman D

机构信息

Department of Obstetrics and Gynaecology, University of Manchester, UK.

出版信息

Symp Soc Exp Biol. 1989;43:325-36.

PMID:2701482
Abstract

Two situations that result in the conversion of human mid-cycle cervical mucus from a sperm-receptive to a sperm-hostile form are described here: firstly, the addition of mucospissic agents, and secondly, the presence of antisperm antibodies. Two mucospissic biguanides were studied, chlorhexidine and Vantocil; both were totally spermicidal in the range 1-10 mg ml-1. Treatment of mucus with 1.5 microM to 1.65 mM Vantocil caused a dose-dependent increase in the dynamic storage modulus. The compatibility of the two biguanides with mucus was examined by measuring the rate of entry of diffusion of the [14C]biguanides into mucus. Chlorhexidine entered the mucus up to 0.53 mM, i.e. the highest concentration used, whilst Vantocil only entered at concentrations below 0.53 mM. This limited entry may be caused by the precipitation of mucus at the interface, producing a barrier of reduced permeability. The behaviour of purified mucin on ultracentrifugation was also altered after treatment with chlorhexidine. The s20 (at 2 mg ml-1 purified mucin) increased from 11.2 S to 19.3 S upon addition of 200 microM chlorhexidine. Further indication of structural alteration of biguanide-treated mucin was given by its loss of solubility in 0.22 M-sodium thiocyanate. The application of these biguanides to vaginal contraception is suggested. When antisperm antibodies are present in either the semen or cervical mucus, we suggest that an interaction can occur between galactose residues on the spermatozoa and galactose recognition sites on the antisperm antibody; in addition, binding can also occur between the Fc region of the antibody and cervical mucus. This process could therefore contribute to the binding of spermatozoa to the antibody and the immobilisation of this complex by the cervical mucus that is seen in immunological infertility. It was shown, by Immunobead binding, that immediate exposure of spermatozoa to D-galactose in the presence of chymotrypsin resulted in a considerable decrease or total loss of bound antisperm antibodies in males who had previously had a high titre of antibody. This reduction in the antibody level on the spermatozoa was accompanied by the appearance of the antibody level on the spermatozoa was accompanied by the appearance of the ability of the spermatozoa to penetrate cervical mucus in those couples examined. This pretreatment regimen for the ejaculate is suggested as a form of therapy for infertility related to the presence of antisperm antibodies.

摘要

本文描述了两种导致人类月经周期中期宫颈黏液从精子接受型转变为精子敌对型的情况

第一,添加黏液浓缩剂;第二,存在抗精子抗体。研究了两种黏液浓缩双胍类药物,洗必泰和Vantocil;两者在1 - 10 mg/ml范围内均具有完全杀精作用。用1.5 microM至1.65 mM的Vantocil处理黏液会导致动态储能模量呈剂量依赖性增加。通过测量[14C]双胍类药物进入黏液的扩散速率来检测这两种双胍类药物与黏液的相容性。洗必泰可进入黏液直至0.53 mM,即所用的最高浓度,而Vantocil仅在浓度低于0.53 mM时进入。这种有限的进入可能是由于黏液在界面处沉淀,形成了一个渗透性降低的屏障。用洗必泰处理后,纯化黏蛋白在超速离心时的行为也发生了改变。在2 mg/ml纯化黏蛋白中加入200 microM洗必泰后,s20从11.2 S增加到19.3 S。双胍类药物处理后的黏蛋白在0.22 M硫氰酸钠中溶解度降低,进一步表明其结构发生了改变。建议将这些双胍类药物应用于阴道避孕。当精液或宫颈黏液中存在抗精子抗体时,我们认为精子上的半乳糖残基与抗精子抗体上的半乳糖识别位点之间可能发生相互作用;此外,抗体的Fc区域与宫颈黏液之间也可能发生结合。因此,这一过程可能导致精子与抗体结合,并使这种复合物在免疫性不孕中被宫颈黏液固定。免疫珠结合试验表明,在存在胰凝乳蛋白酶的情况下,精子立即暴露于D - 半乳糖会导致先前抗体滴度较高的男性精子上结合的抗精子抗体显著减少或完全丧失。精子上抗体水平的这种降低伴随着精子穿透宫颈黏液能力的出现,在这些受检夫妇中观察到了这种情况。建议对射精进行这种预处理方案,作为与抗精子抗体存在相关的不孕症的一种治疗形式。

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