Renal excretion:
Renal filtration accounts for most Medicine excretion. About one fifth of the plasma reaching the glomerulus is filtered through pores in the glomerular endothelium; nearly all water and most electrolytes are passively and actively reabsorbed from the renal tubules back into the circulation. However, polar compounds, which account for most Medicine metabolites, cannot diffuse back into the circulation and are excreted unless a specific transport mechanism exists for their reabsorption (eg, as for glucose, ascorbic acid, and B vitamins). With aging, renal Medicine excretion decreases ; at age 80, clearance is typically reduced to half of what it was at age 30.
The principles of transmembrane passage govern renal handling of Medicines. Medicines bound to plasma proteins remain in the circulation; only unbound Medicine is contained in the glomerular filtrate. Un-ionized forms of Medicines and their metabolites tend to be reabsorbed readily from tubular fluids.
Urine pH, which varies from 4.5 to 8.0, may markedly affect Medicine reabsorption and excretion because urine pH determines the ionization state of a weak acid or base . Acidification of urine increases reabsorption and decreases excretion of weak acids, and, in contrast, decreases reabsorption of weak bases. Alkalinization of urine has the opposite effect. In some cases of overdose, these principles are used to enhance the excretion of weak bases or acids; eg, urine is alkalinized to enhance excretion of acetylsalicylic acid. The extent to which changes in urinary pH alter the rate of Medicine elimination depends on the contribution of the renal route to total elimination, the polarity of the un-ionized form, and the molecule's degree of ionization.
Active tubular secretion in the proximal tubule is important in the elimination of many Medicines. This energy-dependent process may be blocked by metabolic inhibitors. When Medicine concentration is high, secretory transport can reach an upper limit (transport maximum); each substance has a characteristic transport maximum.
Anions and cations are handled by separate transport mechanisms. Normally, the anion secretory system eliminates metabolites conjugated with glycine, sulfate, or glucuronic acid. Anions compete with each other for secretion. This competition can be used therapeutically; eg, probenecid
blocks the normally rapid tubular secretion of penicillin, resulting in higher plasma penicillin concentrations for a longer time. In the cation transport system, cations or organic bases (eg, pramipexole, dofetilide) are secreted by the renal tubules; this process can be inhibited by cimetidine, trimethoprim,prochlorperazine, megestrol, or ketoconazole.
Biliary excretion:
Some Medicines and their metabolites are extensively excreted in bile. Because they are transported across the biliary epithelium against a concentration gradient, active secretory transport is required. When plasma Medicine concentrations are high, secretory transport may approach an upper limit (transport maximum). Substances with similar physicochemical properties may compete for excretion.
Medicines with a molecular weight of > 300 g/mol and with both polar and lipophilic groups are more likely to be excreted in bile; smaller molecules are generally excreted only in negligible amounts. Conjugation, particularly with glucuronic acid, facilitates biliary excretion.
In the enterohepatic cycle, a Medicine secreted in bile is reabsorbed into the circulation from the intestine. Biliary excretion eliminates substances from the body only to the extent that enterohepatic cycling is incomplete—when some of the secreted Medicine is not reabsorbed from the intestine.
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