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肿瘤坏死因子-α和白细胞介素-6可降低大鼠肝细胞胆小管收缩。

Tumor necrosis factor-alpha and interleukin-6 reduce bile canalicular contractions of rat hepatocytes.

作者信息

Ikeda Shinichiro, Mitaka Toshihiro, Harada Keisuke, Sato Fumihiko, Mochizuki Yohichi, Hirata Koichi

机构信息

First Department of Surgery, Cancer Research Institute, Sapporo Medical University School of Medicine, Sapporo, Japan.

出版信息

Surgery. 2003 Jan;133(1):101-9. doi: 10.1067/msy.2003.91.

Abstract

BACKGROUND

Surgeons sometimes encounter hyperbilirubinemia without mechanical obstruction of the biliary tree postoperatively. Many of these patients have bacterial infections and endotoxemia. Kupffer's cells stimulated by endotoxin secrete inflammatory cytokines such as tumor necrosis factor (TNF)-alpha and interleukin (IL)-6. We hypothesized that TNF-alpha and IL-6 might be involved in the pathogenesis of hyperbilirubinemia.

METHODS

Effects of TNF-alpha and IL-6 on the contractions of bile canaliculi (BC) of rat hepatocyte couplets were examined and time-lapse images using phase-contrast microscopy were taken. Bile was collected from rats treated with or without the cytokines. The livers, perfused with lanthanum after the injection of cytokines, were examined ultrastructurally using electron microscopy.

RESULTS

The number of BC contractions decreased in the couplets treated with both cytokines. The rapid movement of a droplet from BC was observed at the intercellular space of the hepatocyte couplet treated with TNF-alpha. Systolic blood pressure and hepatic tissue blood flow of rats injected with TNF-alpha were not changed, whereas the hepatic tissue blood flow of rats treated with IL-6 decreased (Dunnett test, P <.05). Bile secretion was reduced in both groups of rats (Dunnett test, P <.05). In rats treated with TNF-alpha the total serum bile acid concentration increased and lanthanum temporarily accumulated in BC.

CONCLUSIONS

These results suggest that TNF-alpha and IL-6 may reduce BC contractions and thereby decrease bile flow.

摘要

背景

外科医生有时会在术后遇到无胆道机械性梗阻的高胆红素血症。这些患者中的许多人存在细菌感染和内毒素血症。受内毒素刺激的库普弗细胞分泌炎性细胞因子,如肿瘤坏死因子(TNF)-α和白细胞介素(IL)-6。我们推测TNF-α和IL-6可能参与高胆红素血症的发病机制。

方法

检测TNF-α和IL-6对大鼠肝细胞偶联物胆小管(BC)收缩的影响,并使用相差显微镜拍摄延时图像。收集给予或未给予细胞因子处理的大鼠的胆汁。在注射细胞因子后用镧灌注肝脏,然后使用电子显微镜进行超微结构检查。

结果

用两种细胞因子处理的偶联物中BC收缩次数减少。在用TNF-α处理的肝细胞偶联物的细胞间隙处观察到液滴从BC快速移动。注射TNF-α的大鼠的收缩压和肝组织血流量未改变,而用IL-6处理的大鼠的肝组织血流量减少(Dunnett检验,P<.05)。两组大鼠的胆汁分泌均减少(Dunnett检验,P<.05)。在用TNF-α处理的大鼠中,血清总胆汁酸浓度升高,镧暂时积聚在BC中。

结论

这些结果表明,TNF-α和IL-6可能会减少BC收缩,从而减少胆汁流动。

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