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[镰状细胞性状杂合子对能量能力的影响]

[Influence of the sickle cell trait heterozygote on energy abilities].

作者信息

Bitanga E, Rouillon J D

机构信息

Laboratoire des Sciences du Sport, UFR-STAPS de Besançon, Besançon, France.

出版信息

Pathol Biol (Paris). 1998 Jan;46(1):46-52.

PMID:9769936
Abstract

The sickle cell trait (SCT) is a genetic abnormality of the red blood cell which mainly affects people of African descent. It is due to the mutation of only one parental gene (one glutamic acid of the chain beta of the globin is substituted by one valin). The prevalence of SCT in the black US population is within the range of 8-9%. It is increasing in Europe and in Africa where it may reach up to 40% in some regions. The rate of prevalence of SCT in athletic populations was found to be similar to that of the general sedentary population in west African countries. SCT is usually asymptomatic. However, SCT has been associated with a higher risk of sudden death during exercise. In fact, the substitution of one amino-acid modifies the properties of haemoglobin and produces physiological disorders such as sickling, less solubility of the deoxidized form and the reduction of affinity for oxygen. The sickling phenomenon (formation of sickle cells) mainly occurs in some conditions related to the practise of sport (intense and/or prolonged exercise, exercise in hypoxic conditions, exercise in heat conditions). These sickled red blood cells reduce the speed of capillary flow or obstruct the blood vessels which, because of the lack of oxygen, become altered. The physical ability of sickle cell trait carriers (HbAS) who practise sport should be different from the physical ability of subjects with normal haemoglobin (HbAA) because of: 1) potential risks due to their haemoglobinopathy and 2) the eventual modification of their performance ability. These two aspects have caused controversies among many researchers particularly in line with their investigation methods. Nevertheless, the following results seem to be established: 1) the ability to perform sprint exercises is not altered in the HbAS subjects. Their performances in these events are similar to those of HbAA subjects; 2) The ability of HbAS subjects to perform intense and prolonged exercise is decreased. Our former results have shown that prolonged aerobic efforts in hypobaric hypoxic conditions may be associated with a deleterious effect on the performance of HbAS subjects. The damaging consequences on their performance in these conditions could be due to tissue oxygen delivery limitations.

摘要

镰状细胞性状(SCT)是一种红细胞的遗传异常,主要影响非洲裔人群。它是由于仅一个亲本基因发生突变(珠蛋白β链的一个谷氨酸被一个缬氨酸取代)所致。美国黑人人群中SCT的患病率在8%至9%之间。在欧洲和非洲,其患病率正在上升,在某些地区可能高达40%。在西非国家,运动员群体中SCT的患病率与一般久坐人群相似。SCT通常无症状。然而,SCT与运动期间猝死风险较高有关。事实上,一个氨基酸的替换改变了血红蛋白的特性,并产生生理紊乱,如镰状化、脱氧形式的溶解度降低以及对氧气的亲和力降低。镰状化现象(镰状细胞的形成)主要发生在一些与运动相关的情况下(剧烈和/或长时间运动、低氧条件下的运动、高温条件下的运动)。这些镰状红细胞会降低毛细血管血流速度或阻塞血管,由于缺氧,血管会发生改变。由于以下原因,患有镰状细胞性状(HbAS)的运动员的身体能力应该与血红蛋白正常的受试者(HbAA)不同:1)由于其血红蛋白病导致的潜在风险;2)其运动能力的最终改变。这两个方面在许多研究人员中引起了争议,特别是在他们采用的研究方法方面。然而,以下结果似乎已经明确:1)HbAS受试者进行短跑运动的能力没有改变。他们在这些项目中的表现与HbAA受试者相似;2)HbAS受试者进行剧烈和长时间运动的能力下降。我们之前的研究结果表明,在低压低氧条件下进行长时间有氧运动可能会对HbAS受试者的表现产生有害影响。在这些条件下对他们表现的破坏性后果可能是由于组织氧输送受限。

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