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甲基亚硝基脲对成年无特定病原体猫免疫系统和造血系统的影响。

The effects of methylnitrosourea on the immune system and hematopoietic system of adult specific pathogen free cats.

作者信息

Tarr M J, Olsen R G, Hoover E A, Kociba G J, Schaller J P

出版信息

Chem Biol Interact. 1979 Dec;28(2-3):181-99. doi: 10.1016/0009-2797(79)90160-1.

Abstract

The effects of a single non-carcinogenic dose of 15 mg/kg methylnitrosourea (MNU) on the immune and hematopoietic systems of adult specific-pathogen-free (SPF) cats were determined. The cell-mediated-immune (CMI) system was markedly suppressed, as evidenced by: (i) Prolonged cutaneous allograft retention time (41-84 days); (ii) Decreased lymphocyte blast transformation response to mitogens (2% of pretreatment response to pokeweed mitogen or concanavalin A) and antigen (12% of untreated control cat response to keyhole limpet hemocyanin); (iii) Reduced number of absolute erythrocyte-rosetting T-cells in the peripheral blood. This immunosuppression lasted at least 3 months, the duration of the experiment. Suppression of the hematopoietic system was also noted as evidenced by: (i) Peripheral lymphopenia lasting 3 months and neutropenia lasting 3 weeks; (ii) Bone marrow hypocellularity lasting 3 weeks; (iii) Hypoplasia of neutrophilic precursors lasting 3 weeks and erythroid precursors lasting 4 days. It was concluded that a single non-carcinogenic dose of MNU induces a prolonged suppression of the CMI system and a brief suppression of hematopoiesis in adult SPF cats. The immunosuppression may in part be responsible for the previously observed increased susceptibility to feline leukemia virus infection and disease of adult SPF cats treated with MNU.

摘要

研究了给成年无特定病原体(SPF)猫单次给予15 mg/kg非致癌剂量的甲基亚硝基脲(MNU)对其免疫和造血系统的影响。细胞介导免疫(CMI)系统受到明显抑制,表现为:(i)皮肤同种异体移植保留时间延长(41 - 84天);(ii)淋巴细胞对有丝分裂原(对商陆有丝分裂原或刀豆球蛋白A的预处理反应的2%)和抗原(未处理对照猫对钥孔戚血蓝蛋白反应的12%)的母细胞转化反应降低;(iii)外周血中绝对红细胞花环形成T细胞数量减少。这种免疫抑制至少持续了3个月,即实验的持续时间。造血系统的抑制也有体现,表现为:(i)外周淋巴细胞减少持续3个月,中性粒细胞减少持续3周;(ii)骨髓细胞减少持续3周;(iii)嗜中性前体细胞发育不全持续3周,红系前体细胞发育不全持续4天。得出的结论是,单次非致癌剂量的MNU可导致成年SPF猫的CMI系统长期抑制和造血功能短期抑制。这种免疫抑制可能部分解释了先前观察到的接受MNU治疗的成年SPF猫对猫白血病病毒感染和疾病易感性增加的现象。

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