Summary
Female RLEF1/Lati rats were chronically treated with 2-mercaptoethanol in a dose of 13 μg·100 g bw-1·day-1 dissolved in drinking water. During a 48-h experiment 15N-labelled glycine was given orally in a dose of 5 mg 15N·kg bw-1 and urine samples were collected and analysed by an emission spectrometric isotope method. Protein synthesis and nitrogen excretion rate constants were calculated according to the three-pool model, and 3-methylhistidine excretion rates were also determined. 2-Mercaptoethanol appears to influence protein metabolism; however, the slower rates of protein synthesis proved to be apparent in almost all groups of treated rats. Protein synthesis and nitrogen excretion rate constants have exceptionally high values in 2-year-old rats, possibly explained by the occurrence of hypercompensation mechanisms in old age. These were reflected by the excretion rates of 3-methylhistidine which were reduced as a result of sulphhydryl group interactions in age-dependent cellular metabolic changes.
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Abbreviations
- 2ME:
-
2-mercaptoethanol
- 3MeHis:
-
3-methylhistidine
- bw:
-
body weight
- HPLC:
-
high performance liquid chromatography
- SD:
-
standard deviation
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Albrecht, V., Pénzes, L., Petzke, K.J. et al. Relationship between a long-term treatment of 2-mercaptoethanol and protein metabolism in the ageing rat. J Comp Physiol B 162, 547–551 (1992). https://doi.org/10.1007/BF00264816
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DOI: https://doi.org/10.1007/BF00264816