Giblin F J, McCready J P, Schrimscher L, Reddy V N
Eye Research Institute of Oakland University Rochester, MI 48063.
Exp Eye Res. 1987 Jul;45(1):77-91. doi: 10.1016/s0014-4835(87)80080-5.
Previous studies from this laboratory have shown that the normal lens can tolerate exposure to 0.05 mM H2O2 without apparent damage and that this is due in part to an active glutathione redox cycle. The present studies were designed to investigate the role of glutathione reductase in protecting cation transport systems in the lens against potentially damaging effects of peroxide. Pre-treatment of rabbit lenses with 0.5 mM 1.3-bis(2-chloroethyl)-1-nitrosourea (BCNU), a relatively specific inhibitor of glutathione reductase, brought about a 71% inhibition of the enzyme in the capsule-epithelia of the lenses. Subsequent exposure of the lenses for 3 hr to a constant level of 0.05 mM H2O2 in culture medium produced significant accumulation of oxidized glutathione (GSSG) in the lens epithelium and severe effects on the electrolyte balance in the lens, on the activity of Na, K-ATPase and on the accumulation and efflux of 86Rb. The effects included a 35% decrease in activity of Na, K-ATPase, a 10 mM increase in the concentration of Na+ and an 8 mM decrease in K+. BCNU-H2O2 treatment also resulted in loss of transparency of the lenses in the form of vacuoles present in the anterior, subcapsular region, encircling the entire periphery of the organ near the germinative zone of the epithelium. Treatment with either BCNU or 0.05 mM H2O2 alone had only minimal effects on accumulation of GSSG in the epithelium, on lens transparency and on the parameters of cation transport which were investigated. When lenses were treated with 0.05 mM H2O2 alone and then placed in normal medium to measure the accumulation of 86Rb it was found that the cation pump was stimulated 20% above the normal level of activity. Levels of H2O2 higher than 0.05 mM without BCNU pre-treatment produced significant inhibition of Na, K-ATPase and the effects of 0.3 mM H2O2 on cation transport and GSSG accumulation were comparable to those of BCNU-0.05 mM H2O2. While inhibition of the activities of glutathione reductase and Na, K-ATPase in the lenses was found to be irreversible, a partial recovery of the Na+ level and nearly complete recovery of the K+ level were observed when treated lenses were cultured in normal medium for an additional 6 hr. In addition, the rate of efflux of 86Rb which was significantly faster from the BCNU-H2O2-treated lenses compared with the controls, was found to return to the control value during the recovery period.(ABSTRACT TRUNCATED AT 400 WORDS)
本实验室先前的研究表明,正常晶状体能够耐受0.05 mM过氧化氢的暴露而无明显损伤,这部分归因于活跃的谷胱甘肽氧化还原循环。本研究旨在探讨谷胱甘肽还原酶在保护晶状体阳离子转运系统免受过氧化物潜在损伤作用中的作用。用0.5 mM 1,3 - 双(2 - 氯乙基)- 1 - 亚硝基脲(BCNU)预处理兔晶状体,BCNU是谷胱甘肽还原酶相对特异性的抑制剂,可使晶状体囊膜 - 上皮细胞中的该酶活性受到71%的抑制。随后将晶状体在培养基中暴露于恒定水平的0.05 mM过氧化氢3小时,导致晶状体上皮细胞中氧化型谷胱甘肽(GSSG)显著积累,并对晶状体中的电解质平衡、Na,K - ATP酶活性以及86Rb的积累和外流产生严重影响。这些影响包括Na,K - ATP酶活性降低35%,Na+浓度增加10 mM,K+浓度降低8 mM。BCNU - H2O2处理还导致晶状体以位于前囊下区域的空泡形式失去透明度,这些空泡环绕着上皮生发区附近器官的整个周边。单独用BCNU或0.05 mM过氧化氢处理对上皮细胞中GSSG的积累、晶状体透明度以及所研究的阳离子转运参数只有最小的影响。当晶状体仅用0.05 mM过氧化氢处理,然后置于正常培养基中测量86Rb的积累时,发现阳离子泵的活性比正常水平高20%。在没有BCNU预处理的情况下,高于0.05 mM的过氧化氢水平会显著抑制Na,K - ATP酶,0.3 mM过氧化氢对阳离子转运和GSSG积累的影响与BCNU - 0.05 mM过氧化氢的影响相当。虽然发现晶状体中谷胱甘肽还原酶和Na,K - ATP酶的活性抑制是不可逆的,但当处理后的晶状体在正常培养基中再培养6小时时,观察到Na+水平部分恢复,K+水平几乎完全恢复。此外,与对照组相比,BCNU - H2O2处理的晶状体中86Rb的外流速率明显更快,发现在恢复期间其回到了对照值。(摘要截取自400字)