Wazer D E, Rotrosen J
J Pharm Pharmacol. 1984 Dec;36(12):853-4. doi: 10.1111/j.2042-7158.1984.tb04895.x.
[3H]Quinuclidinyl benzilate and [3H]spiperone binding to murine lymphocytes is displaceable but differs from binding to brain receptor sites for these ligands: (1) binding to intact lymphocyte preparations was not saturable; (2) disruption of intact lymphocytes was associated with a marked loss of displaceable ligand binding; (3) drugs differentially displace these ligands in lymphocytes compared to brain. Displaceable binding was increased following incubation of lymphocytes under phospholipid methylating conditions; however, marked effects on cell viability and cell recovery make it difficult to interpret these binding changes. If dopaminergic and cholinergic receptors do exist on lymphocytes, their binding characteristics are profoundly different from comparable cns receptors.
[3H]东莨菪碱季铵盐和[3H]螺哌隆与小鼠淋巴细胞的结合是可置换的,但与这些配体与脑受体位点的结合不同:(1)与完整淋巴细胞制剂的结合不饱和;(2)完整淋巴细胞的破坏与可置换配体结合的显著丧失有关;(3)与脑相比,药物在淋巴细胞中对这些配体的置换作用不同。在磷脂甲基化条件下孵育淋巴细胞后,可置换结合增加;然而,对细胞活力和细胞恢复的显著影响使得难以解释这些结合变化。如果淋巴细胞上确实存在多巴胺能和胆碱能受体,它们的结合特性与中枢神经系统中的类似受体有很大不同。