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多杀巴斯德菌毒素处理的大鼠中生长板面积减小及软骨细胞增殖减少。

Reduced physeal area and chondrocyte proliferation in Pasteurella multocida toxin-treated rats.

作者信息

Ackermann M R, Stabel J R, Pettit R K, Jacobson C D, Elmquist J K, Register K B, Rimler R B, Hilton J H

机构信息

National Animal Disease Center, Ames, IA, USA.

出版信息

Vet Pathol. 1995 Nov;32(6):674-82. doi: 10.1177/030098589503200609.

Abstract

Pasteurella multocida toxin depresses weight gain in rats and pigs. It also affects tissues with rapidly dividing cells. In the present study, we investigated the role of this protein toxin on chondrocyte growth in vivo. Rats were divided into a single- or multiple-dose group and were given, respectively, either a single injection (0.15 or 0.6 micrograms/kg toxin subcutaneously) or multiple injections (0.01-0.2 micrograms/kg subcutaneously) of toxin. Bone (humerus) and other selected tissues were stained for bromodeoxyuridine immunoreactivity (BrDU-IR) in order to gauge cell proliferation. Physeal area was measured in rats from the multiple-dose group. Serum from single- and multiple-dose groups were tested for tumor necrosis factor alpha (TNF-alpha) and interleukin 6 (IL-6) activity using a bioassay system. Decreased weight gain, feed intake, and feed efficiency were observed in single- and multiple-dose groups of rats. Decreased BrDU-IR indices were present in the resting and proliferative zone chondrocytes of the humeral physis in rats from the multiple-dose group, as was decreased physeal area. Increased serum IL-6 bioactivity was present in rats after 24 hours, and no changes in TNF-alpha bioactivity were seen in any group. No alterations in BrDU-IR were seen in rats fed restricted (80% of control) diets. These studies show that sublethal doses of toxin decrease weight gain and affect growth of long bones through suppression of chondrocyte proliferation. These effects may be mediated by direct binding of the toxin to target cells or IL-6 but are not associated with altered feed intake or TNF-induced cachexia.

摘要

多杀巴斯德菌毒素会抑制大鼠和猪的体重增加。它还会影响快速分裂细胞的组织。在本研究中,我们调查了这种蛋白质毒素在体内对软骨细胞生长的作用。将大鼠分为单剂量组或多剂量组,分别给予单次注射(皮下注射0.15或0.6微克/千克毒素)或多次注射(皮下注射0.01 - 0.2微克/千克)毒素。对骨骼(肱骨)和其他选定组织进行溴脱氧尿苷免疫反应性(BrDU - IR)染色,以评估细胞增殖。测量多剂量组大鼠的生长板面积。使用生物测定系统检测单剂量组和多剂量组血清中的肿瘤坏死因子α(TNF - α)和白细胞介素6(IL - 6)活性。在单剂量组和多剂量组大鼠中均观察到体重增加、采食量和饲料效率降低。多剂量组大鼠肱骨生长板静止和增殖区软骨细胞的BrDU - IR指数降低,生长板面积也减小。大鼠在24小时后血清IL - 6生物活性增加,任何组中TNF - α生物活性均无变化。在限制饮食(对照组的80%)的大鼠中未观察到BrDU - IR的改变。这些研究表明,亚致死剂量的毒素会降低体重增加,并通过抑制软骨细胞增殖影响长骨生长。这些作用可能是由毒素与靶细胞的直接结合或IL - 6介导的,但与采食量改变或TNF诱导的恶病质无关。

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