Kropp H, Sundelof J G, Hajdu R, Kahan F M
Antimicrob Agents Chemother. 1982 Jul;22(1):62-70. doi: 10.1128/AAC.22.1.62.
Thienamycin (THM), the N-formimidoyl thienamycin derivative MK0787, and related carbapenem antibiotics were metabolized extensively in mice, rats, rabbits, dogs, rhesus monkeys, and chimpanzees. Urinary recovery of THM ranged from a low of 5% in dogs to 58% in rhesus monkeys. Renal clearance rates in dogs and chimpanzees were unusually low, less than glomerular filtration rates. The reduction in clearance of THM and MK0787 from plasma of rats and rabbits after ligation of renal arteries indicate that the kidneys are responsible for 35 and 92%, respectively, of metabolic drug clearance. Degradation was detected only in kidney homogenates. The enzyme activity was membrane bound and sensitive to inhibitors of Zn-metalloenzymes such as EDTA. A renal dipeptidase, dehydropeptidase-I (DHP-I), EC 3.4.13.11, was found to be responsible for the metabolism of the THM-class antibiotics, which exhibit a structural homology to dehydropeptides. A parallel increase in specific activity against THM and the substrate of DHP-I, glycyldehydrophenylalanine, was observed during solubilization and purification of the enzyme from porcine and human renal cortex. DHP-I was found to catalyze the hydrolysis of the beta-lactam ring in THM and MK0787. The products of the enzyme reaction were identical by high-powered liquid chromatography to their respective metabolites found in the urine. Nonbasic N-acylated THM and natural N-acylated carbapenems (epithienamycins and olivanic acids) were degraded 4- to 50-fold faster than THM when exposed to the enzymatic hydrolysis of DHP-I. Good correlations were obtained between the increased susceptibility of the carbapenem antibiotics to DHP-I as measured in the in vitro enzyme assay and the generally lower recoveries of active antibiotic in the urine of test animals. Despite this unusual degree of metabolism localized in the kidney, the plasma half-life of MK0787 and its efficacy against experimental systemic infections in animals remain satisfactory.
硫霉素(THM)、N-甲脒基硫霉素衍生物MK0787以及相关的碳青霉烯类抗生素在小鼠、大鼠、兔子、狗、恒河猴和黑猩猩体内均有广泛代谢。THM经尿液排泄的回收率在狗体内低至5%,在恒河猴体内为58%。狗和黑猩猩的肾清除率异常低,低于肾小球滤过率。大鼠和兔子肾动脉结扎后,血浆中THM和MK0787清除率的降低表明,肾脏分别负责35%和92%的药物代谢清除。仅在肾脏匀浆中检测到降解。酶活性与膜结合,对锌金属酶抑制剂(如EDTA)敏感。发现一种肾二肽酶,即脱氢肽酶-I(DHP-I,EC 3.4.13.11),负责THM类抗生素的代谢,这类抗生素与脱氢肽具有结构同源性。在从猪和人肾皮质中溶解和纯化该酶的过程中,观察到对THM和DHP-I底物甘氨酰脱氢苯丙氨酸的比活性平行增加。发现DHP-I催化THM和MK0787中β-内酰胺环的水解。酶反应产物通过高效液相色谱法与尿液中各自的代谢物相同。非碱性N-酰化THM和天然N-酰化碳青霉烯类(表硫霉素和奥利万酸)在暴露于DHP-I的酶促水解时,降解速度比THM快4至50倍。在体外酶测定中测得的碳青霉烯类抗生素对DHP-I敏感性增加与试验动物尿液中活性抗生素回收率普遍较低之间存在良好的相关性。尽管这种异常程度的代谢局限于肾脏,但MK0787的血浆半衰期及其对动物实验性全身感染的疗效仍然令人满意。