Shahal Y, Bauminger E R, Zmora E, Katz M, Mazor D, Horn S, Meyerstein N
Dr. Joseph Kaufmann Hematology Laboratory, Corob Research Center, Faculty of Health Sciences, Ben Gurion University of the Negev, Beer Sheva, Israel.
Pediatr Res. 1991 Feb;29(2):119-22. doi: 10.1203/00006450-199102000-00001.
Phenylhydrazine (PHZ) exposure is used to study in vitro red cell aging mechanisms dependent on Hb oxidation. The effect of PHZ on normal neonatal red blood cells was studied in unseparated blood and after separation into light and heavy cells. PHZ caused more extensive morphologic changes in neonatal than in adult red blood cells. PHZ exposure of neonatal cells caused less reduced glutathione depletion than in adult cells. Although we found the same total amount of oxidized Hb in both cells, a well-defined oxidation product of Hb was demonstrated by Mössbauer spectra only in neonatal cells. This oxidation product was not methemoglobin but a trivalent, high-spin iron compound. All neonatal cell populations were more sensitive to PHZ than were adult ones, as demonstrated by the presence of Heinz bodies at low PHZ concentration, which did not affect adult cells. These studies demonstrate greater sensitivity of neonatal cells to PHZ in all density-separated populations.
苯肼(PHZ)暴露用于研究依赖于血红蛋白(Hb)氧化的体外红细胞衰老机制。在未分离的血液以及分离为轻、重细胞后,研究了PHZ对正常新生儿红细胞的影响。与成年红细胞相比,PHZ对新生儿红细胞造成的形态学变化更广泛。新生儿细胞暴露于PHZ后,谷胱甘肽消耗比成年细胞少。尽管我们发现两种细胞中氧化Hb的总量相同,但仅在新生儿细胞中通过穆斯堡尔光谱证实了一种明确的Hb氧化产物。这种氧化产物不是高铁血红蛋白,而是一种三价、高自旋铁化合物。所有新生儿细胞群体对PHZ的敏感性均高于成年细胞群体,低浓度PHZ时出现海因茨小体即可证明,而这对成年细胞没有影响。这些研究表明,在所有密度分离的群体中,新生儿细胞对PHZ更为敏感。