Hepatic growth induced by injection of the liver growth factor into normal rats.

Growth regulation Pub Date : 1994-09-01
J J Díaz Gil, C Rúa, C Machin, R M Cereceda, R García-Cañero, M de Foronda, J Pérez de Diego, C Trilla, P Escartin
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Abstract

Normal Wistar rats injected with the liver growth factor (LGF), a mitogen specific for liver cells, experienced hepatic growth. LGF shows two peaks of activity in vivo, both of them mitogenic. Rats injected either with 6.8 ng or 3.9 micrograms LGF/rat every 3-4 days experienced liver growth showing a see-saw profile. Dry liver weight usually peaked at day 2 (microgram doses) or at day 3 (ng doses) after each injection, with increases of about 30% over controls. Liver DNA synthesis, measured by [3H]-thymidine incorporation, peaked 24 h after LGF injection at both doses. Liver protein synthesis, measured by [14]C-leucine incorporation, usually peaked 24 h after DNA synthesis maximums. Mitogen-stimulated cells were also assessed by immunohistochemical staining for proliferating cell nuclear antigen in livers of LGF-injected rats. Rats injected with rat serum albumin purified from normal rats to serve as controls showed a 6% increase in dry liver weight, but when serum albumin from 3-day fasted rats was injected instead, the increase was not statistically significant. The mild effect of rat serum albumin could be due to the lipid content of the solutions injected, but the level of lipids/mg protein in LGF solutions was half that determined with serum albumin from 3-day fasted rats. From the microscopic and ultramicroscopic studies carried out in rat livers injected with LGF at each dose, we observed: (1) an increase in the number of hepatocytes undergoing mitosis; (2) transient increases in lipid and glycogen contents, as occur after liver resection; (3) no signs of degeneration, such as the appearance of amyloids or fibrosis; (4) no increase in lysosome number, as in hepatotoxicity; (5) no alterations in endothelial or Kupffer cells; and (6) no ultrastructural signs of degeneration either in cytoplasmic organelles (rough endoplasmic reticulum, mitochondria) or in nuclei. One year after LGF injection, rat liver, pancreas, kidneys and spleen were normal, with no signs of degeneration or onset of fibrosis.

注射肝生长因子对正常大鼠肝脏生长的影响。
正常Wistar大鼠注射肝生长因子(LGF),肝细胞特异性丝裂原,经历肝脏生长。LGF在体内表现出两个活性峰,均为有丝分裂活性。每3-4天注射6.8 ng或3.9微克LGF的大鼠肝脏生长呈跷跷板状。干肝重通常在每次注射后第2天(微克剂量)或第3天(ng剂量)达到峰值,比对照组增加约30%。用[3H]-胸腺嘧啶掺入法测定肝脏DNA合成,两种剂量的LGF注射后24小时达到峰值。肝蛋白合成,用c -亮氨酸掺入测定[14],通常在DNA合成达到最大值后24小时达到峰值。用免疫组织化学染色法检测注射了lgf的大鼠肝脏中受丝裂原刺激的细胞增殖细胞核抗原。注射从正常大鼠纯化的大鼠血清白蛋白作为对照,大鼠的干肝重量增加了6%,但当注射3天禁食大鼠的血清白蛋白时,这种增加没有统计学意义。大鼠血清白蛋白的温和作用可能与注射溶液的脂质含量有关,但LGF溶液中脂质/mg蛋白的水平是禁食3天大鼠血清白蛋白测定的一半。通过对注射了不同剂量LGF的大鼠肝脏进行的显微镜和超微显微镜研究,我们观察到:(1)发生有丝分裂的肝细胞数量增加;(2)肝切除后脂质和糖原含量短暂升高;(3)无变性迹象,如淀粉样蛋白或纤维化的出现;(4)不增加溶酶体的数量,如肝毒性;(5)内皮细胞或库普弗细胞无改变;(6)细胞器(粗内质网、线粒体)和细胞核均未见超微结构变性迹象。注射LGF一年后,大鼠肝脏、胰腺、肾脏和脾脏正常,无退行性变或纤维化迹象。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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