Name: Author Spotlight: Investigating Hepatic Adaptations and Prediabetic Progression in Liver Diseases
Uploaded: 2023-10-06T15:00:00
Description: Watch this Scientific Journal Video about Investigating Hepatic Adaptations and Prediabetic Progression in Liver Diseases at JoVE.com

The studies and Nicolai J. Wewer Albrechtsen were supported by Novo Nordisk Foundation Excellence Emerging Investigator Grant - Endocrinology and Metabolism (Application No. NNF19OC0055001), European Foundation for the Study of Diabetes Future Leader Award (NNF21SA0072746) and Independent Research Fund Denmark, Sapere Aude (1052-00003B). Novo Nordisk Foundation Center for Protein Research is supported financially by the Novo Nordisk Foundation (Grant agreement NNF14CC0001). Figure 1B was created with biorender.com.&#160;We thank Dr. Rune E. Kuhre (Novo Nordisk A/S) for fruitful discussions on the perfused mouse liver.&#160;

All animal experiments were conducted with permission from the Danish Animal Experiments Inspectorate, Ministry of Environment and Food of Denmark (permit 2018-15-0201-01397), and the local ethics committee in accordance with the EU directive 2010/63/EU, the National Institutes of Health (publication No. 85-3) and following the guidelines of Danish legislation governing animal experimentation (1987). This is a terminal procedure, and the cause of death is exsanguination and perforation of the diaphragm under deep anesthe...

In Situ Mouse Liver Perfusion Model to Study Metabolic Responses to Substrates

<ol>
	<li>Bale, S. S., Geerts, S., Jindal, R., Yarmush, M. L. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Isolation+and+co-culture+of+rat+parenchymal+and+non-parenchymal+liver+cells+to+evaluate+cellular+interactions+and+response.">Isolation and co-culture of rat parenchymal and non-parenchymal liver cells to evaluate cellular interactions and response.</a> Scientific Reports. 6, 25329 (2016).</li><li>Lauschke, V. M., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Massive+rearrangements+of+cellular+MicroRNA+signatures+are+key+drivers+of+hepatocyte+dedifferentiation.">Massive rearrangements of cellular MicroRNA signatures are key drivers of hepatocyte dedifferentiation.</a> Hepatology. 64 (5), 1743-1756 (2016).</li><li>Seirup, M., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Rapid+changes+in+chromatin+structure+during+dedifferentiation+of+primary+hepatocytes+in+vitro.">Rapid changes in chromatin structure during dedifferentiation of primary hepatocytes in vitro.</a> Genomics. 114 (3), 110330 (2022).</li><li>Gupta, R., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Comparing+in+vitro+human+liver+models+to+in+vivo+human+liver+using+RNA-Seq.">Comparing in vitro human liver models to in vivo human liver using RNA-Seq.</a> Archive of Toxicology. 95 (2), 573-589 (2021).</li><li>Bell, C. C., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Characterization+of+primary+human+hepatocyte+spheroids+as+a+model+system+for+drug-induced+liver+injury,+liver+function,+and+disease.">Characterization of primary human hepatocyte spheroids as a model system for drug-induced liver injury, liver function, and disease.</a> Scientific Reports. 6, 25187 (2016).</li><li>Dewyse, L., Reynaert, H., van Grunsven, L. A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Best+practices+and+progress+in+precision-cut+liver+slice+cultures.">Best practices and progress in precision-cut liver slice cultures.</a> International Journal of Molecular Sciences. 22 (13), 7137 (2021).</li><li>Li, X., George, S. M., Vernetti, L., Gough, A. H., Taylor, D. L. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=A+glass-based,+continuously+zonated+and+vascularized+human+liver+acinus+microphysiological+system+(vLAMPS)+designed+for+experimental+modeling+of+diseases+and+ADME/TOX.">A glass-based, continuously zonated and vascularized human liver acinus microphysiological system (vLAMPS) designed for experimental modeling of diseases and ADME/TOX.</a> Lab on a Chip. 18 (17), 2614-2631 (2018).</li><li>Broutier, L., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Culture+and+establishment+of+self-renewing+human+and+mouse+adult+liver+and+pancreas+3D+organoids+and+their+genetic+manipulation.">Culture and establishment of self-renewing human and mouse adult liver and pancreas 3D organoids and their genetic manipulation.</a> Nature Protocols. 11 (9), 1724-1743 (2016).</li><li>Barto&#353;ek, I., Guaitani, A., Miller, L. L. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=.">.</a> Isolated Liver Perfusion and its Applications. , (1973).</li><li>Gores, G. J., Kost, L. J., LaRusso, N. F. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=The+isolated+perfused+rat+liver:+conceptual+and+practical+considerations.">The isolated perfused rat liver: conceptual and practical considerations.</a> Hepatology. 6 (3), 511-517 (1986).</li><li>Mischinger, H. J., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=An+improved+technique+for+isolated+perfusion+of+rat+livers+and+an+evaluation+of+perfusates.">An improved technique for isolated perfusion of rat livers and an evaluation of perfusates.</a> Journal of Surgical Research. 53 (2), 158-165 (1992).</li><li>Vairetti, M., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Correlation+between+the+liver+temperature+employed+during+machine+perfusion+and+reperfusion+damage:+role+of+Ca2.">Correlation between the liver temperature employed during machine perfusion and reperfusion damage: role of Ca2.</a> Liver Transplantation. 14 (4), 494-503 (2008).</li><li>Ferrigno, A., Richelmi, P., Vairetti, M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Troubleshooting+and+improving+the+mouse+and+rat+isolated+perfused+liver+preparation.">Troubleshooting and improving the mouse and rat isolated perfused liver preparation.</a> Journal of Pharmacological and Toxicological Methods. 67 (2), 107-114 (2013).</li><li>Zawada, R. J. X., Kwan, P., Olszewski, K. L., Llinas, M., Huang, S. -. G. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Quantitative+determination+of+urea+concentrations+in+cell+culture+medium.">Quantitative determination of urea concentrations in cell culture medium.</a> Biochemistry and Cell Biology. 87 (3), 541-544 (2009).</li></ol>

The isolated perfused mouse liver is a strong research tool for studies of the dynamics and molecular mechanisms of hepatic metabolism. The possibility of minute-to-minute sample collection provides a detailed evaluation of the direct effect of a test compound on the liver. Compared to in vivo studies, the perfused liver allows us to study liver metabolism in an isolated manner avoiding extra-hepatic factors carried by the blood and with complete control over the experimental conditions. The advantages of liver ...

The liver is an essential organ in metabolism. It plays a key role in the control of whole-body energy balance by regulating glucose, lipid, and amino acid metabolism. The increase in liver diseases worldwide is emerging as a major global health burden, and more knowledge is needed about the pathophysiology and its consequences for liver functions.
Various in vitro models have been developed for research on the liver to complement in vivo studies. Isolated and cultured primary hepatocytes from rodents and humans are widely used. Non-parenchymal cells can be separated from hepatocytes using differential and gradient centrifugation, and the co-culture of different cell types is useful for studying intercellular crosstalk1. Although primary human hepatocytes are considered the golden standard for testing drug toxicity, several studies have shown that the hepatocytes rapidly dedifferentiate in tissue culture resulting in loss of hepatic functions2,3,4. Hepatocyte culture in a 3D spheroid system ameliorates the dedifferentiation, is more stable, and appears to mimic the liver in vivo to a higher degree than the traditional 2D culture systems5. Precision-cut liver slices are another well-established in vitro model that keeps the tissue architecture intact and contains the non-parenchymal cells present in the liver6. More advanced in vitro models include liver-on-a-chip7 and liver organoids8. However, with all these approaches, there is a loss of structural integrity and flow dynamics, including vectorial portal-hepatic vein flow, which likely impacts the generalizability.
The isolated perfused rat liver was first described by Claude Bernard in 18559, and is still used in various scientific fields for studies of liver biology, toxicology, and pathophysiology. Advantages of the perfused liver compared to the above-mentioned in vitro models include the maintenance of the hepatic architecture, the vascular flow, the hepatocyte polarity and zonation, and the interactions between hepatocytes and non-parenchymal cells. Compared to in vivo studies, the perfused liver allows the study of liver metabolism in an isolated manner avoiding extra-hepatic factors carried by the blood and with complete control over the experimental conditions. Several modifications have been made to improve the rat liver perfusion model over the years10,11,12,13. Although mice have been used for isolated perfused liver studies, less literature is available. Here, we present a method for in situ perfusion of the mouse liver by cannulation of the portal vein and the suprahepatic vena cava inferior to study the acute and direct metabolic responses to metabolic substrates and hormones as measured in the hepatic venous effluent from the mouse liver in real-time.

hepatic glucose production, ureagenesis, and lipolysis quantified using the perfused mouse liver model

The liver has numerous functions, including nutrient metabolism. In contrast to other in vitro and in vivo models of liver research, the isolated perfused liver allows the study of liver biology and metabolism in the whole liver with an intact hepatic architecture, separated from the influence of extra-hepatic factors. Liver perfusions were originally developed for rats, but the method has been adapted to mice as well. Here we describe a protocol for in situ perfusion of the mouse liver. The liver is perfused antegradely through the portal vein with oxygenated Krebs-Henseleit bicarbonate buffer, and the output is collected from the suprahepatic inferior vena cava with clamping of the infrahepatic inferior vena cava to close the circuit. Using this method, the direct hepatic effects of a test compound can be evaluated with a detailed time resolution. Liver function and viability are stable for at least 3 h, allowing the inclusion of internal controls in the same experiment. The experimental possibilities using this model are numerous and may infer insight into liver physiology and liver diseases.

Author Spotlight: Investigating Hepatic Adaptations and Prediabetic Progression in Liver Diseases 

Hepatic Glucose Production, Ureagenesis, and Lipolysis Quantified using the Perfused Mouse Liver Model

In our lab, we investigate how the liver responds to common, as well as rare liver diseases, and how these adaptation may predispose to a pre-diabetogenic state. The liver responds to changes in nutrient availability and concentrations of hormones with increased transcription of relevant genes, but importantly also, with acute and non-transcriptional regulation. With the perfused liver, we can quantify all aspects of metabolism, including the release of metabolites in a minute to minute resolution.Advantages of this technique compared to other in vitro models are that the liver is left in situ with an intact hepatic architecture. And that the liver is viable for at least three hours, allowing each mouse liver to be its own control. Lastly, increasing the translational relevance.Using the mouse perfused liver system, we are able to identify and characterize novel signaling cascade of the hormone glucagon. This may be important as glucagon, as well as other hormone, may play a vital role in the dysmetabolic conditions of the liver in patients with fatty liver disease and diabetes.

A steady baseline is required to determine whether a stimulus or substrate leads to the release of the molecule of interest. Figure 3A shows an example of a successful experiment. Production of urea in the perfused liver is measured in 2 min intervals and shown as mean &#177; SEM. The baseline periods preceding each of the two stimulation periods are steady. The mean urea production during the two stimulation periods and the respective preceding baselines are...

Watch this Scientific Journal Video about Investigating Hepatic Adaptations and Prediabetic Progression in Liver Diseases at JoVE.com

Here, we present a robust method for in situ perfusion of the mouse liver to study the acute and direct regulation of liver metabolism without disturbing the hepatic architecture but in the absence of extra-hepatic factors.

The liver has numerous functions, including nutrient metabolism. In contrast to other in vitro and in vivo models of liver research, the isolated perfused ...