Matsumura T, Kashiwagi T, Meren H, Thurman R G
Eur J Biochem. 1984 Nov 2;144(3):409-15. doi: 10.1111/j.1432-1033.1984.tb08480.x.
Rates of gluconeogenesis from lactate were calculated in periportal and pericentral regions of the liver lobule in perfused rat livers from increases in O2 uptake due to lactate. When lactate (0.1-2.0 mM) was infused into livers from fasted rats perfused in either anterograde or the retrograde direction, a good correlation (r = 0.97) between rates of glucose production and extra O2 uptake by the liver was observed as expected. Rates of oxygen uptake were determined subsequently in periportal and pericentral regions of the liver lobule by placing miniature oxygen electrodes on the liver surface and measuring the local change in oxygen concentration when the flow was stopped. Basal rates of oxygen uptake of 142 +/- 11 and 60 +/- 4 mumol X g-1 X h-1 were calculated for periportal and pericentral regions, respectively. Infusion of 2 mM lactate increased oxygen uptake by 71 mumol X g-1 X h-1 in periportal regions and by 29 mumol X g-1 X h-1 in pericentral areas of the liver lobule. Since the stoichiometry between glucose production and extra oxygen uptake is well-established, rates of glucose production in periportal and pericentral regions of the liver lobule were calculated from local changes in rates of oxygen uptake for the first time. Maximal rates of glucose production from lactate (2 mM) were 60 +/- 7 and 25 +/- 4 mumol X g-1 X h-1 in periportal and pericentral zones of the liver lobule, respectively. The lactate concentrations required for half-maximal glucose synthesis were similar (0.4-0.5 mM) in both regions of the liver lobule in the presence or absence of epinephrine (0.1 microM). In the presence of epinephrine, maximal rates of glucose production from lactate were 79 +/- 5 and 59 +/- 3 mumol X g-1 X h-1 in periportal and pericentral regions, respectively. Thus, gluconeogenesis from lactate predominates in periportal areas of the liver lobule during perfusion in the anterograde direction; however, the stimulation by added epinephrine was greatest in pericentral areas. Differences in local rates of glucose synthesis may be due to ATP availability, as a good correlation between basal rates of O2 uptake and rates of gluconeogenesis were observed in both regions of the liver lobule in the presence and absence of epinephrine. In marked contrast, when livers were perfused in the retrograde direction, glucose production was 28 +/- 5 mumol X g-1 X h-1 in periportal areas and 74 +/- 6 mumol X g-1 X h-1 in pericentral regions.(ABSTRACT TRUNCATED AT 400 WORDS)
根据灌注大鼠肝脏中因乳酸导致的氧气摄取增加情况,计算肝小叶门静脉周围和中央静脉周围区域的乳酸糖异生速率。当将乳酸(0.1 - 2.0 mM)注入正向或逆向灌注的禁食大鼠肝脏时,正如预期的那样,观察到肝脏葡萄糖生成速率与额外氧气摄取之间具有良好的相关性(r = 0.97)。随后,通过将微型氧电极放置在肝脏表面并测量血流停止时局部氧浓度的变化,测定肝小叶门静脉周围和中央静脉周围区域的氧气摄取速率。计算出的门静脉周围和中央静脉周围区域的基础氧气摄取速率分别为142±11和60±4 μmol·g⁻¹·h⁻¹。注入2 mM乳酸可使肝小叶门静脉周围区域的氧气摄取增加71 μmol·g⁻¹·h⁻¹,中央静脉周围区域增加29 μmol·g⁻¹·h⁻¹。由于葡萄糖生成与额外氧气摄取之间的化学计量关系已明确确立,首次根据局部氧气摄取速率的变化计算了肝小叶门静脉周围和中央静脉周围区域的葡萄糖生成速率。来自乳酸(2 mM)的最大葡萄糖生成速率在肝小叶门静脉周围和中央静脉周围区域分别为60±7和25±4 μmol·g⁻¹·h⁻¹。在有或没有肾上腺素(0.1 μM)存在的情况下,肝小叶两个区域中半最大葡萄糖合成所需的乳酸浓度相似(0.4 - 0.5 mM)。在有肾上腺素存在的情况下,来自乳酸的最大葡萄糖生成速率在门静脉周围和中央静脉周围区域分别为79±5和59±3 μmol·g⁻¹·h⁻¹。因此,在正向灌注过程中,肝小叶门静脉周围区域的乳酸糖异生占主导;然而,添加肾上腺素的刺激在中央静脉周围区域最大。局部葡萄糖合成速率的差异可能归因于ATP的可用性,因为在有和没有肾上腺素存在的情况下,在肝小叶的两个区域中都观察到基础氧气摄取速率与糖异生速率之间具有良好的相关性。与之形成鲜明对比的是,当肝脏进行逆向灌注时,门静脉周围区域的葡萄糖生成量为28±5 μmol·g⁻¹·h⁻¹,中央静脉周围区域为74±6 μmol·g⁻¹·h⁻¹。(摘要截断于400字)