Smith G N, Yu L P, Brandt K D, Capello W N
Department of Medicine, Indiana University School of Medicine, Indianapolis 46202-5103, USA.
J Rheumatol. 1998 Mar;25(3):532-5.
To determine whether oral administration of doxycycline in clinically relevant doses will suppress activities of collagenase and gelatinase in extracts of human osteoarthritic (OA) cartilage.
Femoral heads were obtained from 21 patients undergoing arthroplasty for endstage hip OA. Activities of collagenase and gelatinase were measured in extracts of the OA cartilage from patients who received doxycycline, 100 mg bid or qam for 5 days before surgery (n = 5 and n = 6, respectively), 200 mg as a single dose 3 days before surgery (n = 4); or no doxycycline (n = 6).
Five days of doxycycline treatment, in a dose of either 100 mg bid or 100 mg qam, inhibited gelatinase activity in the cartilage extracts (p = 0.003, 0.008, respectively). The bid dose also inhibited collagenase activity (p = 0.002), but inhibition of collagenase with 100 mg qam did not quite reach statistical significance (p = 0.055), in comparison with the values for the untreated OA controls. The single 200 mg dose, given 3 days before procurement of the cartilage, was ineffective in inhibiting metalloproteinase activity.
Oral administration of doxycycline significantly inhibited collagenase and gelatinase activity in human OA cartilage. The effective dose is likely to be well tolerated during chronic administration, e.g., in a clinical trial to assess the potential of the drug to modify cartilage breakdown in OA.
确定临床相关剂量的口服强力霉素是否会抑制人骨关节炎(OA)软骨提取物中胶原酶和明胶酶的活性。
从21例因终末期髋关节OA接受关节置换术的患者获取股骨头。在术前5天接受强力霉素治疗(分别为每日2次,每次100mg或每日1次,每次100mg,n分别为5例和6例)、术前3天接受单次200mg强力霉素治疗(n = 4例)或未接受强力霉素治疗(n = 6例)的患者的OA软骨提取物中测量胶原酶和明胶酶的活性。
5天的强力霉素治疗,剂量为每日2次,每次100mg或每日1次,每次100mg,均可抑制软骨提取物中的明胶酶活性(p分别为0.003和0.008)。每日2次的剂量也可抑制胶原酶活性(p = 0.002),但与未治疗的OA对照组相比,每日1次,每次100mg剂量对胶原酶的抑制作用未达到统计学意义(p = 0.055)。在获取软骨前3天给予单次200mg剂量对抑制金属蛋白酶活性无效。
口服强力霉素可显著抑制人OA软骨中的胶原酶和明胶酶活性。在长期给药期间,例如在评估该药物改变OA中软骨破坏潜力的临床试验中,有效剂量可能具有良好的耐受性。