首页> 外文期刊>The Journal of Physiology >Neutralization of pyrogen-induced tumour necrosis factor by its type 1 soluble receptor in guinea-pigs: effects on fever and interleukin-6 release.
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Neutralization of pyrogen-induced tumour necrosis factor by its type 1 soluble receptor in guinea-pigs: effects on fever and interleukin-6 release.

机译:在豚鼠中通过其1型可溶性受体中和热原诱导的肿瘤坏死因子:对发烧和白介素6释放的影响。

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1. A soluble form of the tumour necrosis factor (TNF) type 1 receptor (referred to as TNF binding protein, TNF-bp) at a dose of 1 mg per animal, or an equivalent volume of solvent, was injected together with 10 microg kg-1 lipopolysaccharide (LPS) or 50 microg kg-1 muramyl-dipeptide (MDP) directly into the arterial circulation of guinea-pigs and the effects on circulating TNF or interleukin-6 (IL-6) and on abdominal temperature were studied. 2. At 15 or 60 min after injection, LPS-induced and MDP-induced circulating TNF was below the detection limit of the assay and thus completely neutralized in animals treated with TNF-bp. In the control group, TNF was still below the limit of detection in most animals 15 min after LPS was injected; in some animals small traces of TNF could already be detected at that time. However, 60 min after administration of LPS, large amounts of TNF (19508 +/- 4682 pg ml-1) were measured in the control group. MDP-induced TNF in plasma was below the limit of detection 15 min after MDP was injected, and rose to 10862 +/- 3029 pg ml-1 60 min after injection. 3. Low levels of circulating IL-6 (20-40 international units (IU) ml-1) were measured in all groups of animals 15 min after injection of LPS or MDP. This value corresponds to the baseline activity of IL-6 in plasma of guinea-pigs. One hour after administration of LPS, IL-6 rose to 5442 +/- 1662 IU ml-1 in the control group and to a significantly lower value of 1485 +/- 179 IU ml-1 in guinea-pigs treated with TNF-bp. One hour after injection of MDP, circulating IL-6 was 2614 +/- 506 IU ml-1 in the control group, while the corresponding value in animals treated with TNF-bp again was significantly lower (873 +/- 312 IU ml-1). 4. The second phase of the characteristic biphasic LPS fever in guinea-pigs was significantly attenuated in animals treated with TNF-bp. The shorter first phase of the febrile response to LPS was identical in both groups of animals. 5. The late phase of MDP-induced fever (7-22 h after injection) was depressed by treatment with TNF-bp, while the first phase of MDP-induced fever (0-7 h after injection) was significantly enhanced by the neutralization of TNF by TNF-bp.
机译:1.以每只动物1 mg的剂量或等体积的溶剂与10 microg一起注射可溶性形式的1型肿瘤坏死因子(TNF)1型受体(称为TNF结合蛋白,TNF-bp)。研究了将kg-1脂多糖(LPS)或50微克kg-1鼠李二肽(MDP)直接引入豚鼠的动脉循环中,并研究了其对循环TNF或白介素6(IL-6)和腹部温度的影响。 2.在注射后15或60分钟,LPS诱导的和MDP诱导的循环TNF低于测定的检测极限,因此在用TNF-bp治疗的动物中被完全中和。在对照组中,注射LPS 15分钟后,大多数动物的TNF仍低于检出限。在某些动物中,那时已经发现了少量的TNF。但是,LPS给药后60分钟,对照组中检测到大量的TNF(19508 +/- 4682 pg ml-1)。注射MDP后15分钟,血浆中MDP诱导的TNF低于检测极限,注射后60分钟上升至10862 +/- 3029 pg ml-1。 3.注射LPS或MDP后15分钟,在所有动物组中均检测到低水平的循环IL-6(20-40国际单位(IU)ml-1)。该值对应于豚鼠血浆中IL-6的基线活性。给予LPS一小时后,对照组的IL-6上升至5442 +/- 1662 IU ml-1,而用TNF-bp治疗的豚鼠的IL-6明显降低至1485 +/- 179 IU ml-1 。注射MDP一小时后,对照组的循环IL-6为2614 +/- 506 IU ml-1,而再次用TNF-bp治疗的动物的相应值则明显降低(873 +/- 312 IU ml- 1)。 4.在用TNF-bp治疗的动物中,豚鼠的特征性双相LPS发烧的第二阶段显着减弱。在两组动物中,对LPS的发热反应的较短的第一阶段是相同的。 5.用TNF-bp治疗可抑制MDP引起的发烧后期(注射后7-22小时),而中和作用可显着增强MDP引起的发烧的第一阶段(注射后0-7小时)。 TNF-bp对TNF的影响。

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