Grzegorzewska A E, Czyzewska K, Szary B
Department of Nephrology, Karol Marcinkowski University School of Medical Sciences, Poznan, Poland.
Adv Perit Dial. 1995;11:33-5.
It was shown elsewhere that in a peritoneally dialyzed woman with pulmonary tuberculosis, oral treatment with rifampicin and pyrazinamide (11 and 25 mg/kg/day, respectively) caused a decrease in the peritoneal transport of sodium, potassium, urea, uric acid, protein, and ultrafiltration rate by 48% to 75% compared to the pretreatment values. Pyrazinoic acid (PA), a metabolite of pyrazinamide, may account for these changes, because rifampicin was also previously used in this patient without peritoneal function impairment. Thus in the present study the influence of PA on the human peritoneum is examined using the modified Ussing-type chamber. PA (1 mg/dL) was introduced into the medium on the interstitial side of the membrane. After the introduction of PA, uric acid transfer from the interstitial to the mesothelial side decreased by about 50%. There were no significant changes in the urea and albumin transfer rates. In conclusion, PA induces changes in uric acid transfer acting directly on mesothelial cells, whereas a decrease in the peritoneal transfer of other solutes may be caused by a decrease in convective transfer rates due to impaired ultrafiltration.
其他研究表明,在一名患有肺结核的腹膜透析女性患者中,口服利福平与吡嗪酰胺(分别为11毫克/千克/天和25毫克/千克/天)导致钠、钾、尿素、尿酸、蛋白质的腹膜转运以及超滤率相较于治疗前的值下降了48%至75%。吡嗪酰胺的代谢产物吡嗪酸(PA)可能是造成这些变化的原因,因为该患者此前也曾使用利福平,但并未出现腹膜功能损害。因此,在本研究中,使用改良的Ussing型小室来研究PA对人腹膜的影响。将PA(1毫克/分升)引入膜间质侧的培养基中。引入PA后,尿酸从间质侧到间皮侧的转运下降了约50%。尿素和白蛋白的转运速率没有显著变化。总之,PA通过直接作用于间皮细胞诱导尿酸转运发生变化,而其他溶质腹膜转运的减少可能是由于超滤受损导致对流转运速率降低所致。