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Nitrogen elimination via the urea cycle is a critical metabolic pathway in mammals and amphibians for detoxifying and excreting excess nitrogen, primarily derived from amino acid catabolism. The urea cycle converts highly toxic ammonia into urea, a much less toxic and water-soluble compound, which is then transported to the kidneys for excretion in urine. The primary function of the urea cycle is to safely remove excess nitrogen from the body by converting ammonia (NH₃), produced during amino acid breakdown, into urea ((NH₂)₂CO). This process prevents toxic accumulation of ammonia in tissues and blood, which can be life-threatening if not efficiently eliminated. The cycle also helps maintain acid-base balance by consuming acidic waste carbon dioxide along with basic ammonia. The urea cycle occurs mainly in hepatocytes (liver cells), with some activity also present in kidney cells. Dysfunction or genetic defects affecting any step can lead to hyperammonemia—a dangerous buildup of ammonia—with severe neurological consequences if untreated.
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