Tyan M L
Mech Ageing Dev. 1982 Sep;20(1):25-32. doi: 10.1016/0047-6374(82)90071-9.
Unlike erythrocytes from elderly humans, red blood cells from old mice are not more sensitive than are cells from young animals to lysis in hypotonic solutions, probably because the mean corpuscular volume decreases rather than increases with age in this species. However, when subjected to an oxidant stress (sodium ascorbate) red blood cells from old animals accumulate more methemoglobin and fewer remain intact than is the case with red blood cells from young mice. The data suggest that this increased vulnerability to oxidative damage is manifest relatively early in the lifespan of red blood cells from old animals and is not solely a property of the older cells. The pathogenesis of the decreased resistance to peroxidation is not known, but it does not appear to be the result of changes in reduced glutathione, NADH: methemoglobin reductase, superoxide dismutase, glutathione reductase, glutamic-oxaloacetic transaminase, or glucose 6-phosphodehydrogenase.
与老年人类的红细胞不同,老年小鼠的红细胞在低渗溶液中并不比幼年动物的细胞更易裂解,这可能是因为该物种的平均红细胞体积随年龄增长而减小而非增大。然而,当受到氧化应激(抗坏血酸钠)时,老年动物的红细胞比幼年小鼠的红细胞积累更多高铁血红蛋白,且保持完整的细胞更少。数据表明,老年动物红细胞对氧化损伤的易感性增加在其红细胞寿命的相对早期就已显现,并非仅仅是衰老细胞的特性。对过氧化抵抗力降低的发病机制尚不清楚,但似乎不是由于还原型谷胱甘肽、NADH:高铁血红蛋白还原酶、超氧化物歧化酶、谷胱甘肽还原酶、谷氨酸草酰乙酸转氨酶或葡萄糖6 -磷酸脱氢酶的变化所致。