新型黄嘌呤衍生物(HWA-138)对脓毒症豚鼠急性肺损伤的衰减作用。

Pharmatherapeutica Pub Date : 1989-01-01
J R Hatherill, M Yonemaru, H Zheng, H Hoffmann, S Fujishima, A Ishizaka, T A Raffin
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引用次数: 0

摘要

黄嘌呤对大肠杆菌和细胞因子诱导的豚鼠肺损伤的保护作用最近得到证实。本研究探讨了黄嘌呤衍生物己酮茶碱类似物HWA-138对脓毒症豚鼠肺损伤的保护作用。三组动物在8小时内进行研究:第一组动物-生理盐水对照,静脉注射3ml 2%赖氨酸/生理盐水,然后连续输注赖氨酸/生理盐水(1ml /kg/hr);II组——脓毒症对照组:静脉注射2 × 10(9)/kg大肠杆菌,随后持续输注赖氨酸/生理盐水(1ml /kg/hr);第三组——E。大肠杆菌败血症加HWA-138连续输注(HWA-138溶解于赖氨酸/生理盐水中),开始时给予大剂量(10mg /kg),然后在注射大肠杆菌前60分钟开始持续输注HWA-138 (3mg /kg/hr)。连续监测动脉血压和白细胞计数8小时。检测肺水(干湿比)、支气管肺泡灌洗液和肺组织中125i标记白蛋白与血浆的浓度比(125i -白蛋白BAL/血浆、125i -白蛋白肺/血浆)。结果表明,静脉注射大肠杆菌可使W/D比升高(p < 0.01),肺/血浆125i白蛋白比升高(p < 0.01)。相比之下,hwa -138治疗组肺W/D比和肺血浆125i白蛋白比均无显著升高(p < 0.01)。这些数据表明,HWA-138可能在减轻败血症引起的肺损伤中发挥作用。
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Attenuation of acute lung injury in septic guinea-pigs by a new xanthine derivative (HWA-138).

The protective effect of xanthines against E. coli-induced and cytokine-induced lung injury in guinea-pigs has been demonstrated recently. In the present study, the possible protective effects were examined of an analogue of pentoxifylline, HWA-138, a xanthine derivative, on lung injury in septic guinea-pigs. Three groups of animals were studied over a period of 8 hours: Group I animals--saline control injected intravenously with 3 ml 2% lysine/normal saline followed by a continuous lysine/saline infusion (1 ml/kg/hr); Group II--septic control injected intravenously with 2 x 10(9)/kg Escherichia coli followed by a continuous lysine/saline infusion (1 ml/kg/hr); and Group III--E. coli septicaemia plus HWA-138 continuous infusion (HWA-138 dissolved in lysine/saline) began with a bolus (10 mg/kg) followed by a HWA-138 continuous infusion (3 mg/kg/hr) started 60 minutes before injection of E. coli. Arterial blood pressure and white blood cell counts were monitored serially for 8 hours. Lung water (wet-to-dry ratio) and the concentration ratio of 125I-labelled albumin in bronchoalveolar lavage (BAL) fluid and lung tissue compared to plasma (125I-albumin BAL/plasma, 125I-albumin lung/plasma) were examined. Results demonstrated that an intravenous injection of E. coli caused an increased W/D ratio (p less than 0.01) and an increased 125I-albumin lung/plasma ratio (p less than 0.01). In contrast, the HWA-138-treated group did not demonstrate significantly increased W/D lung ratios (p less than 0.01) and 125I-albumin lung/plasma ratios (p less than 0.05). The data suggest a possible role for HWA-138 in attenuating sepsis-induced lung injury.

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