The metabolism of urocanic acid, imidazolelactic acid, and D-histidine in the intact rat.
نویسندگان
چکیده
Interest has recently been revived in the possibility that urocanic acid may be an intermediate in the metabolism of L-histidine (1). In the rat, both Cox and Rose (2) and Harrow and Sherwin (3) found this product ineffective in the dietary replacement of histidine. However, neither it nor imidazolelactic acid has been tested for its capacity to promote liver glycogen deposition, which would serve as an index of comparison with another known behavior of n-histidine (4). So far as we are aware, none of the D isomers of the essential amino acids has been tested for its capacity to promote growth when supplied parenterally. This paper records comparative data for glycogen formation after the administration of n-histidine, rAmidazolelactic acid, and urocanic acid. Since such production might well be influenced by differences in rates of absorption, these were also determined. The paper also presents results obtained in tests of growth promotion conducted to determine the capacity of L-histidine, n-histidine, rAmidazolelactic acid, and urocanic acid to supplement a histidine-deficient diet, whether injected subcutaneously or fed.
منابع مشابه
Histidinaemia: a child and his family.
Histidinaemia, an inherited disorder of histidine metabolism, was first described by Ghadimi, Partington, and Hunter in 1961. The principal metabolic pathway for histidine is through urocanic acid and formiminoglutamic acid (FIGLU) to glutamic acid (Fig. 1). Zannoni and La Du (1963) demonstrated that histidase, the enzyme necessary for the conversion of histidine to urocanic acid, was absent fr...
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The major pathway of histidine metabolism in animals and bacteria other than incorporation into protein involves first deamination to urocanic acid, then the anaerobic addition of water to form an intermediate generally considered to be 4(5)imidazolone-5(4)-propionic acid (1, 2). Finally, the ring is split enzymatically to ~formiminoglutamic acid (3) which is converted to free cglutamic acid by...
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Urocanic acid, discovered in 1874 by Jaffe in dog urine (l), has been an evasive compound. The dog from whose urine it was first isolated escaped, and Jaff e was unable to detect urocanic acid in the urine of other dogs or of humans. Subsequently it was observed in the urine of two other dogs (2), but was not found to be a regular constituent of canine or human urine (2, 3). The isolation of an...
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ورودعنوان ژورنال:
- The Journal of biological chemistry
دوره 202 1 شماره
صفحات -
تاریخ انتشار 1953