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Arginine synthesis and

Fig. 3. Proline and arginine synthesis and degradation to show interrelationships between the pathways. The structures are glutamic acid (GLU), ornithine (ORN), citrulline (CIT), arginine (ARG), urea. 2-oxo-5-amino valeric acid (OAV), A -pyrroline-2-carboxylic acid (P2C), proline (PRO), A -pyrroline-5-carboxylic acid (P5C), glutamic semialdehyde (GSA). Fig. 3. Proline and arginine synthesis and degradation to show interrelationships between the pathways. The structures are glutamic acid (GLU), ornithine (ORN), citrulline (CIT), arginine (ARG), urea. 2-oxo-5-amino valeric acid (OAV), A -pyrroline-2-carboxylic acid (P2C), proline (PRO), A -pyrroline-5-carboxylic acid (P5C), glutamic semialdehyde (GSA).
Logically, ADH receptor antagonists, and ADH synthesis and release inhibitors can be effective aquaretics. ADH, 8-arginine vasopressin [113-79-17, is synthesized in the hypothalamus of the brain, and is transported through the supraopticohypophyseal tract to the posterior pituitary where it is stored. Upon sensing an increase of plasma osmolaUty by brain osmoreceptors or a decrease of blood volume or blood pressure detected by the baroreceptors and volume receptors, ADH is released into the blood circulation it activates vasopressin receptors in blood vessels to raise blood pressure, and vasopressin V2 receptors of the nephrons of the kidney to retain water and electrolytes to expand the blood volume. [Pg.211]

Figure 31-3. Arginine, ornithine, and proline metabolism. Reactions with solid arrows all occur in mammalian tissues. Putrescine and spermine synthesis occurs in both mammals and bacteria. Arginine phosphate of invertebrate muscle functions as a phosphagen analogous to creatine phosphate of mammalian muscle (see Figure 31-6). Figure 31-3. Arginine, ornithine, and proline metabolism. Reactions with solid arrows all occur in mammalian tissues. Putrescine and spermine synthesis occurs in both mammals and bacteria. Arginine phosphate of invertebrate muscle functions as a phosphagen analogous to creatine phosphate of mammalian muscle (see Figure 31-6).
Wiesinger, H., Arginine metabolism and the synthesis of nitric oxide in the nervous system, Prog. Neurobiol. 64 (2001), p. 365-391... [Pg.278]

An anomaly associated with citrulline that became evident when detailed kinetic studies were made in the 1950s (R.B. Fisher and J.R. Bronk) was the irreproducibility of its catalytic activity in liver slices on the formation of urea, despite the clear evidence from Ratner and Petrack of its importance in arginine synthesis. Initially the discrepancy in catalytic activity between ornithine and citrulline was ascribed to the possible impermeability of the liver cell plasma membrane to the latter intermediate, a hypothesis which was rapidly disproved experimentally. Only recently has it been shown that ornithine transcarbamylase is clearly associated with the ornithine/... [Pg.108]

B. Rzeszotarska u. E. Masuikiewicz, Arginine, Histidine and Tryptophane in Peptide Synthesis. The Imidazole Function of Histidine, Org. Prep. Proced. Int. 21, 393-450 (1989). [Pg.820]

Baich, A. Vogel, H.J. N-Acetyl-y-glutamokinase and N-acetylglutamic y-semialdehyde dehydrogenase repressible enzymes of arginine synthesis in Escherichia coh. Biochem. Biophys. Res. Commun., 7, 491-496 (1962)... [Pg.346]

Synthesis of NO Arginine, 02, and NADPH are substrates for cytosolic NO synthase (Figure 13.9). Flavin mononucleotide (FMN), flavin adenine dinucleotide (FAD), heme, and tetrahydro- biopterin are coenzymes for the enzyme, and NO and citrulline are products of the reaction. Three NO synthases have been identified. Two are constitutive (synthesized at a constant rate regardless of physiologic demand), Ca2+-calmodulin-dependent enzymes. They are found primarily in endothelium (eNOS), and neural tissue... [Pg.148]

Synthesis of Arginine and Ornithine and the 1407 1. Synthesis and Catabolism of Cysteine... [Pg.1358]

C. Synthesis and Catabolism of Proline, Ornithine, Arginine, and Polyamines... [Pg.1374]


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Arginine synthesis

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