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Correction of glutathione deficiency in the lower respiratory tract of HIV seropositive individuals by glutathione aerosol treatment.通过谷胱甘肽气雾剂治疗纠正HIV血清阳性个体下呼吸道中的谷胱甘肽缺乏症。
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The level and half-life of glutathione in human plasma.人体血浆中谷胱甘肽的水平及半衰期。
FEBS Lett. 1980 Nov 3;120(2):209-11. doi: 10.1016/0014-5793(80)80299-7.
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Enhancement of the primary antibody response by 2-mercaptoethanol is mediated by its action on glutathione in the serum.
Eur J Immunol. 1980 May;10(5):391-5. doi: 10.1002/eji.1830100514.
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Accurate quantification of cells recovered by bronchoalveolar lavage.支气管肺泡灌洗回收细胞的准确量化。
Am Rev Respir Dis. 1984 Oct;130(4):650-8. doi: 10.1164/arrd.1984.130.4.650.
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Glutathione.谷胱甘肽
Annu Rev Biochem. 1983;52:711-60. doi: 10.1146/annurev.bi.52.070183.003431.
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Lymphocyte dysfunction after DNA damage by toxic oxygen species. A model of immunodeficiency.有毒氧物种造成DNA损伤后的淋巴细胞功能障碍。一种免疫缺陷模型。
J Exp Med. 1986 Mar 1;163(3):746-51. doi: 10.1084/jem.163.3.746.
6
Hypothyroidism protects against free radical damage in ischemic acute renal failure.甲状腺功能减退可预防缺血性急性肾衰竭中的自由基损伤。
Kidney Int. 1986 Jun;29(6):1162-6. doi: 10.1038/ki.1986.122.
7
Prevention of doxorubicin myocardial toxicity in mice by reduced glutathione.还原型谷胱甘肽对小鼠阿霉素心肌毒性的预防作用
Cancer Res. 1986 May;46(5):2551-6.
8
Thiol containing antioxidant drugs and the human immune system.含硫醇的抗氧化药物与人体免疫系统。
Bull Eur Physiopathol Respir. 1987 Jul-Aug;23(4):303-7.
9
Estimation of volume of epithelial lining fluid recovered by lavage using urea as marker of dilution.使用尿素作为稀释标志物通过灌洗回收的上皮衬液体积的估计。
J Appl Physiol (1985). 1986 Feb;60(2):532-8. doi: 10.1152/jappl.1986.60.2.532.
10
D-penicillamine inhibits transactivation of human immunodeficiency virus type-1 (HIV-1) LTR by transactivator protein.D-青霉胺可抑制反式激活蛋白对人免疫缺陷病毒1型(HIV-1)长末端重复序列的反式激活作用。
FEBS Lett. 1988 Aug 29;236(2):282-6. doi: 10.1016/0014-5793(88)80038-3.

通过谷胱甘肽气雾剂治疗纠正HIV血清阳性个体下呼吸道中的谷胱甘肽缺乏症。

Correction of glutathione deficiency in the lower respiratory tract of HIV seropositive individuals by glutathione aerosol treatment.

作者信息

Holroyd K J, Buhl R, Borok Z, Roum J H, Bokser A D, Grimes G J, Czerski D, Cantin A M, Crystal R G

机构信息

Pulmonary Branch, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, Maryland 20892.

出版信息

Thorax. 1993 Oct;48(10):985-9. doi: 10.1136/thx.48.10.985.

DOI:10.1136/thx.48.10.985
PMID:8256245
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC464806/
Abstract

BACKGROUND

Concentrations of glutathione, a ubiquitous tripeptide with immune enhancing and antioxidant properties, are decreased in the blood and lung epithelial lining fluid of human immunodeficiency virus (HIV) seropositive individuals. Since the lung is the most common site of infection in those who progress to AIDS it is rational to consider whether it is possible to safely augment glutathione levels in the epithelial lining fluid of HIV seropositive individuals, thus potentially improving local host defence.

METHODS

Purified reduced glutathione was delivered by aerosol to HIV seropositive individuals (n = 14) and the glutathione levels in lung epithelial lining fluid were compared before and at one, two, and three hours after aerosol administration.

RESULTS

Before treatment total glutathione concentrations in the epithelial lining fluid were approximately 60% of controls. After three days of twice daily doses each of 600 mg reduced glutathione, total glutathione levels in the epithelial lining fluid increased and remained in the normal range for at least three hours after treatment. Strikingly, even though > 95% of the glutathione in the aerosol was in its reduced form, the percentage of oxidised glutathione in epithelial lining fluid increased from 5% before treatment to about 40% three hours after treatment, probably reflecting the use of glutathione as an antioxidant in vivo. No adverse effects were observed.

CONCLUSIONS

It is feasible and safe to use aerosolised reduced glutathione to augment the deficient glutathione levels of the lower respiratory tract of HIV seropositive individuals. It is rational to evaluate further the efficacy of this tripeptide in improving host defence in HIV seropositive individuals.

摘要

背景

谷胱甘肽是一种普遍存在的具有免疫增强和抗氧化特性的三肽,在人类免疫缺陷病毒(HIV)血清阳性个体的血液和肺上皮衬液中浓度降低。由于肺部是那些进展为艾滋病患者最常见的感染部位,因此有理由考虑是否有可能安全地提高HIV血清阳性个体上皮衬液中的谷胱甘肽水平,从而潜在地改善局部宿主防御能力。

方法

将纯化的还原型谷胱甘肽通过气雾剂给予HIV血清阳性个体(n = 14),并比较气雾剂给药前、给药后1小时、2小时和3小时肺上皮衬液中的谷胱甘肽水平。

结果

治疗前,上皮衬液中的总谷胱甘肽浓度约为对照组的60%。每天两次给予600 mg还原型谷胱甘肽,连续三天后,上皮衬液中的总谷胱甘肽水平升高,治疗后至少三小时保持在正常范围内。引人注目的是,尽管气雾剂中> 95%的谷胱甘肽为还原形式,但上皮衬液中氧化型谷胱甘肽的百分比从治疗前的5%增加到治疗后三小时的约40%,这可能反映了谷胱甘肽在体内作为抗氧化剂的作用。未观察到不良反应。

结论

使用雾化还原型谷胱甘肽来提高HIV血清阳性个体下呼吸道缺乏的谷胱甘肽水平是可行且安全的。进一步评估这种三肽在改善HIV血清阳性个体宿主防御方面的疗效是合理的。