Prall Amy K, Longo G Matthew, Mayhan William G, Waltke Eugene A, Fleckten Beverly, Thompson Robert W, Baxter B Timothy
Department of Surgery, University of Nebraska Medical Center, Omaha, NE 68114, USA.
J Vasc Surg. 2002 May;35(5):923-9. doi: 10.1067/mva.2002.123757.
Doxycycline has been shown to inhibit aneurysm formation in a rodent model of abdominal aortic aneurysm (AAA). The doses necessary for this inhibition (6 mg/kg) are much higher than the standard antibiotic doses (1 to 1.5 mg/kg) used in humans. Because the side effects associated with doxycycline are dose related, whether patients would tolerate doses that are four to six times higher than normal is unclear. Also unclear is whether the serum levels necessary in these animal models can be safely achieved in patients. The purposes of this study were to determine the serum concentrations necessary to inhibit aneurysm formation in a mouse model of AAA and to compare them with the plasma concentrations in patients with AAA with a standard dose of doxycycline.
Four groups of 10 mice of C57BL/6 strain were given doxycycline (0, 10, 50, and 100 mg/kg) beginning at 7 weeks of age. At 8 weeks of age, the mice underwent AAA induction through bathing periadventitial aortic tissue with 0.25 mol/L CaCl(2). Blood samples were taken 10 weeks after surgery to assess the levels of doxycycline. Aortic size was measured at AAA induction and at death with a videomicrometer. Fourteen patients with diagnosed AAA were given 100 mg of doxycycline twice a day for at least 3 months. Blood samples to determine the plasma levels of the drug were taken at 3 or 6 months. The circulating levels of doxycycline for mice and humans were assessed with high-performance liquid chromatography.
The changes in aortic size and circulating levels of doxycycline in the AAA murine model are reported. Doses of 10, 50, and 100 mg/kg accounted for a 33%, 44%, and 66% reduction of the aneurysmal growth in the mice, respectively. In patients, the circulating doxycycline levels ranged from 1.8 to 9.42 microg/mL (mean, 4.14 +/- 0.557), values similar to those obtained in mice.
The circulating doxycycline levels of the patients are comparable with those achieved in mice. Doxycycline accounts for an inhibition of 33% to 66% of the aortic growth. The findings suggest that standard doxycycline doses could inhibit AAA growth in humans.
在腹主动脉瘤(AAA)啮齿动物模型中,强力霉素已被证明可抑制动脉瘤形成。产生这种抑制作用所需的剂量(6毫克/千克)远高于人类使用的标准抗生素剂量(1至1.5毫克/千克)。由于与强力霉素相关的副作用与剂量有关,尚不清楚患者是否能耐受比正常剂量高4至6倍的剂量。同样不清楚的是,在这些动物模型中所需的血清水平在患者身上能否安全达到。本研究的目的是确定在AAA小鼠模型中抑制动脉瘤形成所需的血清浓度,并将其与接受标准剂量强力霉素的AAA患者的血浆浓度进行比较。
四组每组10只C57BL/6品系小鼠,从7周龄开始给予强力霉素(0、10、50和100毫克/千克)。8周龄时,通过用0.25摩尔/升氯化钙浸泡主动脉外膜组织诱导小鼠发生AAA。术后10周采集血样以评估强力霉素水平。在诱导AAA时和处死时用视频显微镜测量主动脉大小。14例确诊为AAA的患者每天两次给予100毫克强力霉素,至少持续3个月。在3或6个月时采集血样以测定药物的血浆水平。用高效液相色谱法评估小鼠和人类体内强力霉素的循环水平。
报告了AAA小鼠模型中主动脉大小和强力霉素循环水平的变化。10、50和100毫克/千克的剂量分别使小鼠动脉瘤生长减少33%、44%和66%。在患者中,强力霉素的循环水平在1.8至9.42微克/毫升之间(平均为4.14±0.557),与在小鼠中获得的值相似。
患者体内强力霉素的循环水平与小鼠体内的相当。强力霉素可抑制33%至66%的主动脉生长。这些发现表明标准剂量的强力霉素可抑制人类AAA的生长。