Insulin’s effect on the liver: "Direct or indirect" continues to be the question
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《临床调查学报》
Institut Cochin, Departement Endocrinologie, Metabolisme et Cancer, UMR 8104 CNRS, U 567 INSERM, Universite Rene Descartes, Faculte de Medecine, Paris, France.
Abstract
Previous studies suggest that insulin can inhibit hepatic glucose production (HGP) by both direct and indirect actions. The indirect effects include inhibition of glucagon secretion, reduction in plasma nonesterified fatty acid levels, reduction of the amount of gluconeogenic precursor supplied to the liver, and change in neural input to the liver. A study in this issue of the JCI demonstrates that, in overnight-fasted dogs, an acute, selective increase of portal insulin induces a rapid inhibition of HGP, and a 4-fold rise in head insulin level does not enhance the inhibition of HGP in response to portal insulin infusion. This study demonstrates that insulin’s direct effects on the liver dominate the control of HGP. These data balance previous studies in mice that suggested that indirect effects of insulin via the hypothalamus are the primary determinant of HGP.
See the related article beginning on page 521
Introduction
For a long time it was believed that the inhibition of hepatic glucose production (HGP) by insulin resulted only from a direct effect of the hormone on the liver. However, 2 observations challenged this view: (a) whereas insulin is a potent inhibitor of HGP in vivo, the hormone is relatively ineffective in vitro in rodent liver (1), suggesting that insulin primarily acts on an extrahepatic tissue; and (b) peripheral insulin infusion in humans and dogs is just as effective as intraportal insulin infusion in suppressing HGP (2-4), suggesting that insulin can inhibit HGP by both direct and indirect actions (reviewed in ref. 5).
Indirect action of insulin on HGP
The indirect effects of insulin on HGP could be explained by its actions on pancreatic cells, adipose tissue, and skeletal muscles. Insulin inhibits glucagon secretion from pancreatic cells, thereby decreasing HGP (6, 7). Adipose tissue and muscles are exquisitely sensitive to the inhibitory effect of insulin on lipolysis and proteolysis. Insulin induces a decrease in the release of nonesterified fatty acids and glycerol from adipose tissue (8) and gluconeogenic precursors from skeletal muscles (9), thus causing a decrease in hepatic gluconeogenesis. More recently, insulin action on the brain has been demonstrated to play a role in the regulation of HGP (10): infusion of insulin in the third cerebral ventricle of rats reduces HGP. The blockade of insulin receptors in the rodent hypothalamus (by injection of antisense oligonucleotides that inhibit insulin receptor expression) impairs the ability of insulin to inhibit HGP (11).
Direct and dominant action of insulin on HGP
The best in vivo demonstration of a direct effect of insulin on HGP comes from studies in overnight-fasted dogs in which changes in portal plasma insulin, in the absence of changes in plasma glucagon, nonesterified fatty acid, or gluconeogenic precursors, effectively inhibit HGP (12). The study reported by Edgerton et al. in this issue of the JCI confirms these data and demonstrates that insulin’s direct effects on the liver dominate the control of HGP in overnight-fasted dogs (13). In addition, the authors show that a 4-fold rise in head insulin level does not enhance the inhibition of HGP in response to portal insulin infusion. The importance of the insulin receptor for the direct actions of insulin on HGP was supported by the observation that, in liver-specific insulin receptor knockout (LIRKO) mice, high-dose insulin fails to suppress HGP (14), but these results have been questioned, since the long-term absence of the insulin receptor may have induced an adaptive phenotype. This was supported by the finding that even upon restoration of insulin receptors to the livers of LIRKO mice, insulin was not able to suppress HGP (15). This led to the conclusion that both the direct and the indirect effects of insulin on HGP require an intact insulin-signaling pathway in liver.
How do we reconcile the investigations performed in rodents and in dogs
It is now widely accepted that insulin inhibits HGP by both direct and indirect pathways (5), but controversy remains concerning which pathway exerts the dominant effect. In this issue of the JCI, Edgerton and colleagues provide convincing evidence that the direct effects of insulin on HGP are dominant in overnight-fasted dogs and that the indirect effects of insulin on the brain are of minor importance (13). In contrast, Rossetti and coworkers (10, 16) have provided robust evidence to support the existence of an indirect effect of insulin on HGP via the hypothalamus. Recently, a number of methodological and physiological considerations have been proposed to underlie the apparent complexity of insulin’s observed actions on HGP (5). In particular, basal HGP is 10–15 times greater (per kilogram of body weight) in mice than in dogs, while plasma glucagon levels are similar. It is possible that, in mice, the liver does have substantial neural input in the basal state and the removal of hepatic insulin receptors leads to increased neural control of HGP as a protective response. Another possible explanation is that, in overnight-fasted dogs, hepatic gluconeogenesis (as opposed to hepatic glycogenolysis) contributes to less than 50% of HGP, whereas it contributes to approximately 80–90% of HGP in rodents. In mice fasted for 4 hours and 24 hours, hepatic glycogenolysis contributed to less than 10–20% of HGP (17). As hepatic gluconeogenesis is much less sensitive to inhibition by insulin than glycogenolysis (18), it could be suggested that, in mice, efficient inhibition of hepatic gluconeogenesis by insulin requires basal inputs from the CNS. Several lines of evidence suggest that an autonomic neural input to the liver can modulate liver metabolism (19, 20). When insulin levels are increased via a systemic insulin infusion, the activation of central ATP-dependent potassium channels is required for the inhibition of HGP (16). It has been suggested that descending fibers within the hepatic branch of the vagus nerve could vehiculate autonomic neural input to the liver to modulate liver metabolism. Indeed, the inhibition of central fat oxidation, which, like insulin infusion, inhibits HGP, is largely accounted for by a marked inhibition of gluconeogenesis (21). Furthermore, hepatic vagotomy abolishes the effects of inhibition of central fat oxidation on HGP (21). It could be of interest to investigate whether the inhibition of HGP in response to insulin infusion is due to an inhibition of gluconeogenesis and whether hepatic vagotomy abolishes this effect.
It is possible that in overnight-fasted dogs, acute changes in plasma insulin have a predominantly direct effect on glycogenolysis, whereas at later time points insulin may inhibit gluconeogenesis by a predominantly indirect mechanism (secondary to an inhibition of lipolysis in adipose tissue and of proteolysis in skeletal muscle, which reduces the amount of FFAs, glycerol, and amino acids reaching the liver; see ref. 12).
Concluding remarks
The relative importance of direct and/or indirect effects of insulin on HGP could have implications for diabetes treatment. Indeed, the enhanced HGP observed in type 2 diabetes patients is primarily due to an increase in gluconeogenesis (22). As gluconeogenesis is much less sensitive than glycogenolysis to the inhibition by insulin, hepatic insulin resistance observed in type 2 diabetics could be due simply to the enhanced gluconeogenesis and not necessarily to a defect in insulin signaling. If this is true, a rational therapeutic approach for the correction of HGP in type 2 diabetes would be an inhibition of gluconeogenesis. Plasma glucagon levels are increased throughout the day in type 2 diabetic patients despite hyperglycemia (23), and glucagon stimulates gluconeogenic enzyme gene expression (24). This could explain the predominance of this pathway in the liver of type 2 diabetics. Recently, it has been shown that glucagon-like peptide-1, in addition to its well-known effect on the stimulation of insulin secretion, was able to inhibit glucagon secretion (25). This molecule could have promising effects for the treatment of increased HGP seen in type 2 diabetes.
Footnotes
Nonstandard abbreviations used: HGP, hepatic glucose production.
Conflict of interest: The author has declared that no conflict of interest exists.
References
Williamson, J., Wright, P., Malaisse, W., and Ashmore, J. 1966. . Control of gluconeogenesis by acetyl CoA in rats treated with glucagon and anti-insulin serum. Biochem. Biophys. Res. Commun. 22::765-770.
Ader, M., and Bergman, R. 1990. . Peripheral effects of insulin dominate suppression of fasting hepatic glucose production. Am. J. Physiol. 258::E1020-E1032.
Giacca, A. et al. 1992. . Importance of peripheral insulin levels for insulin-induced suppression of glucose production in depancreatized dogs. J. Clin. Invest. 90::1769-1777.
Lewis, G.F., Zinman, B., Groenewoud, Y., Vranic, M., and Giacca, A. 1996. . Hepatic glucose production is regulated both by direct hepatic and extrahepatic effects of insulin in humans. Diabetes. 45::454-462.
Cherrington, A.D. 2005. . The role of hepatic insulin receptors in the regulation of glucose production. J. Clin. Invest. 115::1136-1139. doi:10.1172/JCI200525152.
Ishihara, H., Maechler, P., Gjinovci, A., Herrera, P.L., and Wollheim, C.B. 2003. . Islet -cell secretion determines glucagon release from neighbouring alpha-cells. Nat. Cell Biol. 5::330-335.
Diao, J., Asghar, Z., Chan, C.B., and Wheeler, M.B. 2005. . Glucose-regulated glucagon secretion requires insulin receptor expression in pancreatic alpha-cells. J. Biol. Chem. 280::33487-33496.
Sindelar, D.K. et al. 1997. . The role of fatty acids in mediating the effects of peripheral insulin on hepatic glucose production in the conscious dog. Diabetes. 46::187-196.
Sindelar, D.K., Balcom, J.H., Chu, C.A., Neal, D.W., and Cherrington, A.D. 1996. . A comparison of the effects of selective increases in peripheral or portal insulin on hepatic glucose production in the conscious dog. Diabetes. 45::1594-1604.
Obici, S., Feng, Z., Karkanias, G., Baskin, D.G., and Rossetti, L. 2002. . Decreasing hypothalamic insulin receptors causes hyperphagia and insulin resistance in rats. Nat. Neurosci. 5::566-572.
Buettner, C. et al. 2005. . Severe impairment in liver insulin signaling fails to alter hepatic insulin action in conscious mice. J. Clin. Invest. 115::1306-1313. doi:10.1172/JCI200523109.
Cherrington, A. 1999. . Control of glucose uptake and release by the liver in vivo. Diabetes. 48::1198-1214.
Edgerton, D.S. et al. 2006. . Insulin’s direct effects on the liver dominate the control of hepatic glucose production. J. Clin. Invest. 116::521-527. doi:10.1172/JCI27073.
Fisher, S.J., and Kahn, C.R. 2003. . Insulin signaling is required for insulin’s direct and indirect action on hepatic glucose production. J. Clin. Invest. 111::463-468. doi:10.1172/JCI200316426.
Okamoto, H., Obici, S., Accili, D., and Rossetti, L. 2005. . Restoration of liver insulin signaling in Insr knockout mice fails to normalize hepatic insulin action. J. Clin. Invest. 115::1314-1322. doi:10.1172/JCI200523096.
Obici, S., Zhang, B.B., Karkanias, G., and Rossetti, L. 2002. . Hypothalamic insulin signaling is required for inhibition of glucose production. Nat. Med. 8::1376-1382.
Burgess, S.C. et al. 2005. . Effect of murine strain on metabolic pathways of glucose production after brief or prolonged fasting. Am. J. Physiol. 289::E53-E61.
Chiasson, J.L., Liljenquist, J.E., Finger, F.E., and Lacy, W.W. 1976. . Differential sensitivity of glycogenolysis and gluconeogenesis to insulin infusion in dogs. Diabetes. 25::283-291.
Shimazu, T. 1987. . Neuronal regulation of hepatic glucose metabolism in mammals. Diabetes Metab. Rev. 3::185-206.
Jungermann, K. et al. 1987. . Regulation of liver metabolism by hepatic nerves. Adv. Enzyme Regul. 26::63-88.
Pocai, A., Obici, S., Schwartz, G., and Rossetti, L. 2005. . A brain-liver circuit regulates glucose homeostasis. Cell Metab. 1::53-61.
Magnusson, I., Rothman, D.L., Katz, L.D., Shulman, R.G., and Shulman, G.I. 1992. . Increased rate of gluconeogenesis in type-II diabetes-mellitus. A 13C nuclear magnetic resonance study. J. Clin. Invest. 90::1323-1327.
Reaven, G.M., Chen, Y.D.I., Golay, A., Swislocki, A.L., and Jaspan, J.B. 1987. . Documentation of hyperglucagonemia throughout the day in non-obese and obese patients with non-insulin-dependent diabetes mellitus. J. Clin. Endocrinol. Metab. 64::106-110.
Granner, D.K., and Pilkis, S.J. 1990. . The genes of hepatic glucose metabolism. J. Biol. Chem. 265::10173-10176.
Drucker, D.J. 2002. . Biologic actions and therapeutic potential of the proglucagon-derived peptides. Gastroenterology. 122::531-544.(Jean Girard)
Abstract
Previous studies suggest that insulin can inhibit hepatic glucose production (HGP) by both direct and indirect actions. The indirect effects include inhibition of glucagon secretion, reduction in plasma nonesterified fatty acid levels, reduction of the amount of gluconeogenic precursor supplied to the liver, and change in neural input to the liver. A study in this issue of the JCI demonstrates that, in overnight-fasted dogs, an acute, selective increase of portal insulin induces a rapid inhibition of HGP, and a 4-fold rise in head insulin level does not enhance the inhibition of HGP in response to portal insulin infusion. This study demonstrates that insulin’s direct effects on the liver dominate the control of HGP. These data balance previous studies in mice that suggested that indirect effects of insulin via the hypothalamus are the primary determinant of HGP.
See the related article beginning on page 521
Introduction
For a long time it was believed that the inhibition of hepatic glucose production (HGP) by insulin resulted only from a direct effect of the hormone on the liver. However, 2 observations challenged this view: (a) whereas insulin is a potent inhibitor of HGP in vivo, the hormone is relatively ineffective in vitro in rodent liver (1), suggesting that insulin primarily acts on an extrahepatic tissue; and (b) peripheral insulin infusion in humans and dogs is just as effective as intraportal insulin infusion in suppressing HGP (2-4), suggesting that insulin can inhibit HGP by both direct and indirect actions (reviewed in ref. 5).
Indirect action of insulin on HGP
The indirect effects of insulin on HGP could be explained by its actions on pancreatic cells, adipose tissue, and skeletal muscles. Insulin inhibits glucagon secretion from pancreatic cells, thereby decreasing HGP (6, 7). Adipose tissue and muscles are exquisitely sensitive to the inhibitory effect of insulin on lipolysis and proteolysis. Insulin induces a decrease in the release of nonesterified fatty acids and glycerol from adipose tissue (8) and gluconeogenic precursors from skeletal muscles (9), thus causing a decrease in hepatic gluconeogenesis. More recently, insulin action on the brain has been demonstrated to play a role in the regulation of HGP (10): infusion of insulin in the third cerebral ventricle of rats reduces HGP. The blockade of insulin receptors in the rodent hypothalamus (by injection of antisense oligonucleotides that inhibit insulin receptor expression) impairs the ability of insulin to inhibit HGP (11).
Direct and dominant action of insulin on HGP
The best in vivo demonstration of a direct effect of insulin on HGP comes from studies in overnight-fasted dogs in which changes in portal plasma insulin, in the absence of changes in plasma glucagon, nonesterified fatty acid, or gluconeogenic precursors, effectively inhibit HGP (12). The study reported by Edgerton et al. in this issue of the JCI confirms these data and demonstrates that insulin’s direct effects on the liver dominate the control of HGP in overnight-fasted dogs (13). In addition, the authors show that a 4-fold rise in head insulin level does not enhance the inhibition of HGP in response to portal insulin infusion. The importance of the insulin receptor for the direct actions of insulin on HGP was supported by the observation that, in liver-specific insulin receptor knockout (LIRKO) mice, high-dose insulin fails to suppress HGP (14), but these results have been questioned, since the long-term absence of the insulin receptor may have induced an adaptive phenotype. This was supported by the finding that even upon restoration of insulin receptors to the livers of LIRKO mice, insulin was not able to suppress HGP (15). This led to the conclusion that both the direct and the indirect effects of insulin on HGP require an intact insulin-signaling pathway in liver.
How do we reconcile the investigations performed in rodents and in dogs
It is now widely accepted that insulin inhibits HGP by both direct and indirect pathways (5), but controversy remains concerning which pathway exerts the dominant effect. In this issue of the JCI, Edgerton and colleagues provide convincing evidence that the direct effects of insulin on HGP are dominant in overnight-fasted dogs and that the indirect effects of insulin on the brain are of minor importance (13). In contrast, Rossetti and coworkers (10, 16) have provided robust evidence to support the existence of an indirect effect of insulin on HGP via the hypothalamus. Recently, a number of methodological and physiological considerations have been proposed to underlie the apparent complexity of insulin’s observed actions on HGP (5). In particular, basal HGP is 10–15 times greater (per kilogram of body weight) in mice than in dogs, while plasma glucagon levels are similar. It is possible that, in mice, the liver does have substantial neural input in the basal state and the removal of hepatic insulin receptors leads to increased neural control of HGP as a protective response. Another possible explanation is that, in overnight-fasted dogs, hepatic gluconeogenesis (as opposed to hepatic glycogenolysis) contributes to less than 50% of HGP, whereas it contributes to approximately 80–90% of HGP in rodents. In mice fasted for 4 hours and 24 hours, hepatic glycogenolysis contributed to less than 10–20% of HGP (17). As hepatic gluconeogenesis is much less sensitive to inhibition by insulin than glycogenolysis (18), it could be suggested that, in mice, efficient inhibition of hepatic gluconeogenesis by insulin requires basal inputs from the CNS. Several lines of evidence suggest that an autonomic neural input to the liver can modulate liver metabolism (19, 20). When insulin levels are increased via a systemic insulin infusion, the activation of central ATP-dependent potassium channels is required for the inhibition of HGP (16). It has been suggested that descending fibers within the hepatic branch of the vagus nerve could vehiculate autonomic neural input to the liver to modulate liver metabolism. Indeed, the inhibition of central fat oxidation, which, like insulin infusion, inhibits HGP, is largely accounted for by a marked inhibition of gluconeogenesis (21). Furthermore, hepatic vagotomy abolishes the effects of inhibition of central fat oxidation on HGP (21). It could be of interest to investigate whether the inhibition of HGP in response to insulin infusion is due to an inhibition of gluconeogenesis and whether hepatic vagotomy abolishes this effect.
It is possible that in overnight-fasted dogs, acute changes in plasma insulin have a predominantly direct effect on glycogenolysis, whereas at later time points insulin may inhibit gluconeogenesis by a predominantly indirect mechanism (secondary to an inhibition of lipolysis in adipose tissue and of proteolysis in skeletal muscle, which reduces the amount of FFAs, glycerol, and amino acids reaching the liver; see ref. 12).
Concluding remarks
The relative importance of direct and/or indirect effects of insulin on HGP could have implications for diabetes treatment. Indeed, the enhanced HGP observed in type 2 diabetes patients is primarily due to an increase in gluconeogenesis (22). As gluconeogenesis is much less sensitive than glycogenolysis to the inhibition by insulin, hepatic insulin resistance observed in type 2 diabetics could be due simply to the enhanced gluconeogenesis and not necessarily to a defect in insulin signaling. If this is true, a rational therapeutic approach for the correction of HGP in type 2 diabetes would be an inhibition of gluconeogenesis. Plasma glucagon levels are increased throughout the day in type 2 diabetic patients despite hyperglycemia (23), and glucagon stimulates gluconeogenic enzyme gene expression (24). This could explain the predominance of this pathway in the liver of type 2 diabetics. Recently, it has been shown that glucagon-like peptide-1, in addition to its well-known effect on the stimulation of insulin secretion, was able to inhibit glucagon secretion (25). This molecule could have promising effects for the treatment of increased HGP seen in type 2 diabetes.
Footnotes
Nonstandard abbreviations used: HGP, hepatic glucose production.
Conflict of interest: The author has declared that no conflict of interest exists.
References
Williamson, J., Wright, P., Malaisse, W., and Ashmore, J. 1966. . Control of gluconeogenesis by acetyl CoA in rats treated with glucagon and anti-insulin serum. Biochem. Biophys. Res. Commun. 22::765-770.
Ader, M., and Bergman, R. 1990. . Peripheral effects of insulin dominate suppression of fasting hepatic glucose production. Am. J. Physiol. 258::E1020-E1032.
Giacca, A. et al. 1992. . Importance of peripheral insulin levels for insulin-induced suppression of glucose production in depancreatized dogs. J. Clin. Invest. 90::1769-1777.
Lewis, G.F., Zinman, B., Groenewoud, Y., Vranic, M., and Giacca, A. 1996. . Hepatic glucose production is regulated both by direct hepatic and extrahepatic effects of insulin in humans. Diabetes. 45::454-462.
Cherrington, A.D. 2005. . The role of hepatic insulin receptors in the regulation of glucose production. J. Clin. Invest. 115::1136-1139. doi:10.1172/JCI200525152.
Ishihara, H., Maechler, P., Gjinovci, A., Herrera, P.L., and Wollheim, C.B. 2003. . Islet -cell secretion determines glucagon release from neighbouring alpha-cells. Nat. Cell Biol. 5::330-335.
Diao, J., Asghar, Z., Chan, C.B., and Wheeler, M.B. 2005. . Glucose-regulated glucagon secretion requires insulin receptor expression in pancreatic alpha-cells. J. Biol. Chem. 280::33487-33496.
Sindelar, D.K. et al. 1997. . The role of fatty acids in mediating the effects of peripheral insulin on hepatic glucose production in the conscious dog. Diabetes. 46::187-196.
Sindelar, D.K., Balcom, J.H., Chu, C.A., Neal, D.W., and Cherrington, A.D. 1996. . A comparison of the effects of selective increases in peripheral or portal insulin on hepatic glucose production in the conscious dog. Diabetes. 45::1594-1604.
Obici, S., Feng, Z., Karkanias, G., Baskin, D.G., and Rossetti, L. 2002. . Decreasing hypothalamic insulin receptors causes hyperphagia and insulin resistance in rats. Nat. Neurosci. 5::566-572.
Buettner, C. et al. 2005. . Severe impairment in liver insulin signaling fails to alter hepatic insulin action in conscious mice. J. Clin. Invest. 115::1306-1313. doi:10.1172/JCI200523109.
Cherrington, A. 1999. . Control of glucose uptake and release by the liver in vivo. Diabetes. 48::1198-1214.
Edgerton, D.S. et al. 2006. . Insulin’s direct effects on the liver dominate the control of hepatic glucose production. J. Clin. Invest. 116::521-527. doi:10.1172/JCI27073.
Fisher, S.J., and Kahn, C.R. 2003. . Insulin signaling is required for insulin’s direct and indirect action on hepatic glucose production. J. Clin. Invest. 111::463-468. doi:10.1172/JCI200316426.
Okamoto, H., Obici, S., Accili, D., and Rossetti, L. 2005. . Restoration of liver insulin signaling in Insr knockout mice fails to normalize hepatic insulin action. J. Clin. Invest. 115::1314-1322. doi:10.1172/JCI200523096.
Obici, S., Zhang, B.B., Karkanias, G., and Rossetti, L. 2002. . Hypothalamic insulin signaling is required for inhibition of glucose production. Nat. Med. 8::1376-1382.
Burgess, S.C. et al. 2005. . Effect of murine strain on metabolic pathways of glucose production after brief or prolonged fasting. Am. J. Physiol. 289::E53-E61.
Chiasson, J.L., Liljenquist, J.E., Finger, F.E., and Lacy, W.W. 1976. . Differential sensitivity of glycogenolysis and gluconeogenesis to insulin infusion in dogs. Diabetes. 25::283-291.
Shimazu, T. 1987. . Neuronal regulation of hepatic glucose metabolism in mammals. Diabetes Metab. Rev. 3::185-206.
Jungermann, K. et al. 1987. . Regulation of liver metabolism by hepatic nerves. Adv. Enzyme Regul. 26::63-88.
Pocai, A., Obici, S., Schwartz, G., and Rossetti, L. 2005. . A brain-liver circuit regulates glucose homeostasis. Cell Metab. 1::53-61.
Magnusson, I., Rothman, D.L., Katz, L.D., Shulman, R.G., and Shulman, G.I. 1992. . Increased rate of gluconeogenesis in type-II diabetes-mellitus. A 13C nuclear magnetic resonance study. J. Clin. Invest. 90::1323-1327.
Reaven, G.M., Chen, Y.D.I., Golay, A., Swislocki, A.L., and Jaspan, J.B. 1987. . Documentation of hyperglucagonemia throughout the day in non-obese and obese patients with non-insulin-dependent diabetes mellitus. J. Clin. Endocrinol. Metab. 64::106-110.
Granner, D.K., and Pilkis, S.J. 1990. . The genes of hepatic glucose metabolism. J. Biol. Chem. 265::10173-10176.
Drucker, D.J. 2002. . Biologic actions and therapeutic potential of the proglucagon-derived peptides. Gastroenterology. 122::531-544.(Jean Girard)