Sestier C, Odent-Pogu S, Bonneville M, Maurel C, Lang F, Sai P
Immunol Lett. 1985;10(1):57-60. doi: 10.1016/0165-2478(85)90051-3.
This study concerns the effect of a 12-day cyclosporin A (CsA) treatment (50 mg per kg per day) on "autoimmune" diabetes induced by 5 low doses (40 mg per kg per day) of streptozotocin (SZ). The SZ-treatment period was initiated 4 days after initial administration of CsA. In young (45-day) CD-1 male mice, CsA enhanced hyperglycemia, hypoinsulinemia and beta-cell destruction following a multiple low-dosage SZ. Moreover, CsA did not prevent development of insulitis induced concomitantly by SZ. Similarly, CsA enhanced the "toxic" diabetes produced by a single high dose (160 mg/kg) of SZ. Furthermore, in the absence of SZ, CsA alone induced glucose intolerance, associated with beta-cell degranulation and high pancreatic CsA content. The enhancement of SZ-induced diabetes by CsA may thus be due to toxicity of the immunosuppressive agent for pancreatic beta cells. This side effect is noteworthy because CsA is currently being used in the therapy of human insulin-dependent diabetes.
本研究关注为期12天的环孢素A(CsA)治疗(每天每千克50毫克)对5次低剂量(每天每千克40毫克)链脲佐菌素(SZ)诱导的“自身免疫性”糖尿病的影响。在首次给予CsA 4天后开始进行SZ治疗期。在年轻(45日龄)的CD-1雄性小鼠中,CsA在多次低剂量SZ给药后加剧了高血糖、低胰岛素血症和β细胞破坏。此外,CsA未能预防SZ同时诱导的胰岛炎的发展。同样,CsA加剧了单次高剂量(160毫克/千克)SZ产生的“毒性”糖尿病。此外,在没有SZ的情况下,单独使用CsA会导致葡萄糖不耐受,这与β细胞脱颗粒和胰腺中高含量的CsA有关。因此,CsA对SZ诱导的糖尿病的加剧可能是由于免疫抑制剂对胰腺β细胞的毒性。这种副作用值得关注,因为CsA目前正用于人类胰岛素依赖型糖尿病的治疗。