Hougen H P, Thygesen P, Christensen H B, Rygaard J, Svendsen O, Juul P
University Institute of Forensic Pathology, Copenhagen, Denmark.
Int J Immunopharmacol. 1992 Aug;14(6):1113-23. doi: 10.1016/0192-0561(92)90157-g.
Guanethidine sulphate causes destruction of peripheral sympathetic neurons and infiltration of mononuclear inflammatory cells in the sympathetic ganglia of both athymic nude (rnu/rnu) and euthymic LEW/Mol rats. The effect of guanethidine is believed to be an autoimmune reaction. To determine the effect of immunosuppressive drugs concurrently with guanethidine treatment both athymic and euthymic rats were treated with guanethidine 40 mg/kg i.p. daily for 14 days, cyclophosphamide 100 mg/kg i.p. on days 1 and 8, methylprednisolone 10 mg/kg and cyclosporin A 10 mg/kg daily from days 1 to 7, and then every other day from days 8 to 14. The number of neurons in the sympathetic ganglia was counted and four subpopulations of mononuclear inflammatory cells were identified by monoclonal antibodies MHC II, CD8 T-cells/NK-cells, CD5 T-cells, CD4 T-cells/macrophages. Our results show that the immunosuppressive drugs used were unable to prevent the guanethidine-induced reduction of sympathetic neurons, although the number, of neurons following guanethidine-methylprednisolone treatment was significantly higher compared with guanethidine alone in both athymic and euthymic rats. The identification of mononuclear cells in the sympathetic ganglia showed that the CD8/NK and CD5 populations were the populations primarily responding to guanethidine treatment. Both CD8/NK and CD5 populations were absent without guanethidine, but increased significantly following guanethidine in both athymic and euthymic animals. None of the immunosuppressive drugs used could prevent the guanethidine-induced rise in the CD8/NK population in neither athymic nor in euthymic rats. The rise in the CD5 population was suppressed following treatment with all immunosuppressive drugs in athymic rats, but only following methylprednisolone in euthymic animals. These results indicate that guanethidine induces proliferation of T-cells in euthymic rats and non-functional CD5 positive pre T-cells in athymic animals. The CD5 population in both athymic and euthymic animals appears relatively more sensitive to immunosuppressive drugs than the NK-cell population also activated by guanethidine. This relatively resistant NK-cell population seems to play an important role in the guanethidine-induced destruction of sympathetic neurons and can explain why the guanethidine-induced immunological reaction could not be fully prevented by the immunosuppressive drugs used. The conclusion is that guanethidine induces destruction of sympathetic neurons by a NK-cell-mediated reaction.
硫酸胍乙啶会导致无胸腺裸鼠(rnu/rnu)和有胸腺的LEW/Mol大鼠的交感神经节中周围交感神经元的破坏以及单核炎性细胞的浸润。胍乙啶的这种作用被认为是一种自身免疫反应。为了确定免疫抑制药物与胍乙啶联合治疗的效果,对无胸腺和有胸腺的大鼠均腹腔注射40mg/kg胍乙啶,每日1次,共14天;在第1天和第8天腹腔注射100mg/kg环磷酰胺;从第1天至第7天每日腹腔注射10mg/kg甲基泼尼松龙和10mg/kg环孢素A,然后从第8天至第14天隔日注射。对交感神经节中的神经元数量进行计数,并通过单克隆抗体MHC II、CD8 T细胞/NK细胞、CD5 T细胞、CD4 T细胞/巨噬细胞鉴定单核炎性细胞的四个亚群。我们的结果表明,尽管在无胸腺和有胸腺的大鼠中,胍乙啶-甲基泼尼松龙联合治疗后的神经元数量比单独使用胍乙啶时显著增加,但所用的免疫抑制药物无法预防胍乙啶引起的交感神经元减少。交感神经节中单核细胞的鉴定表明,CD8/NK和CD5亚群是主要对胍乙啶治疗产生反应的亚群。在未使用胍乙啶时,CD8/NK和CD5亚群均不存在,但在无胸腺和有胸腺的动物中使用胍乙啶后均显著增加。所用的免疫抑制药物均无法预防无胸腺和有胸腺大鼠中胍乙啶引起的CD8/NK亚群增加。在无胸腺大鼠中,所有免疫抑制药物治疗后CD5亚群的增加均受到抑制,但在有胸腺的动物中仅甲基泼尼松龙治疗后CD5亚群的增加受到抑制。这些结果表明,胍乙啶在有胸腺的大鼠中诱导T细胞增殖,在无胸腺的动物中诱导无功能的CD5阳性前T细胞增殖。无胸腺和有胸腺动物中的CD5亚群似乎比同样被胍乙啶激活的NK细胞亚群对免疫抑制药物相对更敏感。这种相对耐药的NK细胞亚群似乎在胍乙啶诱导的交感神经元破坏中起重要作用,并且可以解释为什么所用的免疫抑制药物无法完全预防胍乙啶诱导的免疫反应。结论是胍乙啶通过NK细胞介导的反应诱导交感神经元的破坏。