Cook-Mills J M, Cohen R L, Perlman R L, Chambers D A
Center for Molecular Biology of Oral Diseases, University of Illinois at Chicago, USA.
Immunology. 1995 Aug;85(4):544-9.
The effects of noradrenaline and other adrenergic agonists on lymphocyte activation were studied. Spleen and thymus cells from BALB/c mice were stimulated by mitogens and lymphocyte activation was monitored by measuring the incorporation of [methyl-3H]thymidine into DNA. Noradrenaline, adrenaline, isoproterenol and dopamine all inhibited the activation of spleen and thymus cells by concanavalin A, a T-cell specific mitogen, and the activation of spleen cells by lipopolysaccharide, a T-independent B-cell mitogen. The various catecholamines were approximately equipotent, having IC50 of approximately 10 microM. alpha-adrenergic agonists (phenylephrine, clonidine) did not inhibit lymphocyte activation. Noradrenaline, adrenaline and isoproterenol also inhibited DNA synthesis in S49 T lymphoma cells. The effects of adrenergic receptor antagonists on lymphocyte function were also studied. The inhibition of lymphocyte activation by catecholamines could not be reversed by antagonists to beta-adrenergic receptors (propranolol), alpha-adrenergic receptors (phentolamine), or dopaminergic receptors (haloperidol). Experiments with human peripheral blood leucocytes revealed that, as with murine cells, the beta-adrenergic antagonists propranolol and nadalol did not affect the catecholamine-mediated inhibition of lymphocyte activation. Although lymphocytes contain beta-adrenergic receptors that are coupled to adenylyl cyclase activity, catecholamines appear to inhibit murine lymphocyte activation by a mechanism that is independent of these or other classical adrenergic receptors.
研究了去甲肾上腺素和其他肾上腺素能激动剂对淋巴细胞活化的影响。用丝裂原刺激BALB/c小鼠的脾细胞和胸腺细胞,并通过测量[甲基-3H]胸腺嘧啶核苷掺入DNA来监测淋巴细胞活化。去甲肾上腺素、肾上腺素、异丙肾上腺素和多巴胺均抑制T细胞特异性丝裂原伴刀豆球蛋白A对脾细胞和胸腺细胞的活化,以及非T细胞依赖性B细胞丝裂原脂多糖对脾细胞的活化。各种儿茶酚胺的作用大致相当,IC50约为10微摩尔。α-肾上腺素能激动剂(去氧肾上腺素、可乐定)不抑制淋巴细胞活化。去甲肾上腺素、肾上腺素和异丙肾上腺素也抑制S49 T淋巴瘤细胞中的DNA合成。还研究了肾上腺素能受体拮抗剂对淋巴细胞功能的影响。β-肾上腺素能受体拮抗剂(普萘洛尔)、α-肾上腺素能受体拮抗剂(酚妥拉明)或多巴胺能受体拮抗剂(氟哌啶醇)均不能逆转儿茶酚胺对淋巴细胞活化的抑制作用。对人外周血白细胞的实验表明,与鼠细胞一样,β-肾上腺素能拮抗剂普萘洛尔和纳多洛尔不影响儿茶酚胺介导的淋巴细胞活化抑制。尽管淋巴细胞含有与腺苷酸环化酶活性偶联的β-肾上腺素能受体,但儿茶酚胺似乎通过一种独立于这些或其他经典肾上腺素能受体的机制抑制鼠淋巴细胞活化。