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儿茶酚胺的持续体内治疗通过α介导机制抑制大鼠外周血T淋巴细胞的体外反应性。

Continuous in vivo treatment with catecholamines suppresses in vitro reactivity of rat peripheral blood T-lymphocytes via alpha-mediated mechanisms.

作者信息

Felsner P, Hofer D, Rinner I, Mangge H, Gruber M, Korsatko W, Schauenstein K

机构信息

Department of Functional Pathology, School of Medicine, University of Graz, Austria.

出版信息

J Neuroimmunol. 1992 Mar;37(1-2):47-57. doi: 10.1016/0165-5728(92)90154-d.

Abstract

A 20 h continuous treatment of rats with catecholamines, using subcutaneously implantable retard tablets, had either no (adrenaline, isoproterenol, midodrine) or a slight (noradrenaline) suppressive effect on the in vitro responsiveness of peripheral blood T-lymphocytes. A marked suppression of the mitogen response ensued when adrenaline, noradrenaline or midodrine, but not isoproterenol, was applied together with the beta-receptor blocker propranolol, whereas the combination with the alpha-receptor blocker phentolamine had no effect. The mitogen response of splenic lymphocytes was not affected by any of these treatments. This alpha-mediated adrenergic suppression of peripheral blood T-cells was not correlated with general metabolic alterations, shifts in white blood cell counts or CD4+/CD8+ subsets, or with elevated glucocorticoid levels. The data suggest that to consistently influence the reactivity of rat peripheral blood lymphocytes by chronic adrenergic stimuli in vivo requires both high catecholamine levels and a bias towards alpha-adrenergic receptivity.

摘要

使用可皮下植入的缓释片对大鼠进行20小时的儿茶酚胺连续治疗,对体外外周血T淋巴细胞反应性的影响,肾上腺素、异丙肾上腺素、米多君无影响,去甲肾上腺素仅有轻微抑制作用。当肾上腺素、去甲肾上腺素或米多君(而非异丙肾上腺素)与β受体阻滞剂普萘洛尔联合应用时,有丝分裂原反应受到显著抑制,而与α受体阻滞剂酚妥拉明联合应用则无作用。脾淋巴细胞的有丝分裂原反应不受这些治疗的任何影响。外周血T细胞的这种α介导的肾上腺素能抑制作用与一般代谢改变、白细胞计数或CD4+/CD8+亚群的变化或糖皮质激素水平升高无关。数据表明,在体内通过慢性肾上腺素能刺激持续影响大鼠外周血淋巴细胞的反应性,既需要高儿茶酚胺水平,也需要偏向α肾上腺素能受体敏感性。

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