Literature DB >> 15339746

Time course of the hepatic adaptation to TPN: interaction with glycogen depletion.

Sheng-Song Chen1, Carlos J Torres-Sanchez, Nadeen Hosein, Yiqun Zhang, D Brooks Lacy, Owen P McGuinness.   

Abstract

In response to chronic (5 days) TPN, the liver becomes a major site of glucose disposal, removing approximately 45% (4.5 mg.kg(-1).min(-1)) of exogenous glucose. Moreover, approximately 70% of glucose is not stored but released as lactate. We aimed to determine in chronically catheterized conscious dogs the time course of adaptation to TPN and the glycogen depletion impact on early time course. After an 18-h (n = 5) fast, TPN was infused into the inferior vena cava for 8 (n = 5) or 24 h (n = 6). A third group, of 42-h-fasted animals (n = 6), was infused with TPN for 8 h. TPN was infused at a rate designed to match the dog's calculated basal energy and nitrogen requirements. NHGU (-2.3 +/- 0.1 to 2.2 +/- 0.7 to 3.9 +/- 0.6 vs. -1.7 +/- 0.3 to 1.1 +/- 0.5 to 2.9 +/- 0.4 mg.kg(-1).min(-1), basal to 4 to 8 h, 18 vs. 42 h) and net hepatic lactate release (0.7 +/- 0.3 to 0.6 +/- 0.1 to 1.4 +/- 0.2 vs. -0.6 +/- 0.1 to 0.1 +/- 0.1 to 0.8 +/- 0.1 mg.kg(-1).min(-1), basal to 4 to 8 h) increased progressively. Net hepatic glycogen repletion and tracer determined that glycogen syntheses were similar. After 24 h of TPN, NHGU (5.4 +/- 0.6 mg.kg(-1).min(-1)) and net hepatic lactate release (2.6 +/- 0.4 mg.kg(-1).min(-1)) increased further. In summary, 1) most hepatic adaptation to TPN occurs within 24 h after initiation of TPN, and 2) prior glycogen depletion does not augment hepatic adaptation rate.

Entities:  

Mesh:

Substances:

Year:  2004        PMID: 15339746     DOI: 10.1152/ajpendo.00192.2004

Source DB:  PubMed          Journal:  Am J Physiol Endocrinol Metab        ISSN: 0193-1849            Impact factor:   4.310


  6 in total

Review 1.  Physiologic action of glucagon on liver glucose metabolism.

Authors:  C J Ramnanan; D S Edgerton; G Kraft; A D Cherrington
Journal:  Diabetes Obes Metab       Date:  2011-10       Impact factor: 6.577

2.  Continuous low-dose fructose infusion does not reverse glucagon-mediated decrease in hepatic glucose utilization.

Authors:  Paulette M Johnson; Sheng-Song Chen; Tammy S Santomango; Phillip E Williams; D Brooks Lacy; Owen P McGuinness
Journal:  Metabolism       Date:  2010-10-12       Impact factor: 8.694

3.  Glucagon-mediated impairments in hepatic and peripheral tissue nutrient disposal are not aggravated by increased lipid availability.

Authors:  Sheng-Song Chen; Tammy S Santomango; Phillip E Williams; D Brooks Lacy; Owen P McGuinness
Journal:  Am J Physiol Endocrinol Metab       Date:  2009-02-10       Impact factor: 4.310

4.  A physiological increase in the hepatic glycogen level does not affect the response of net hepatic glucose uptake to insulin.

Authors:  Jason J Winnick; Zhibo An; Mary Courtney Moore; Christopher J Ramnanan; Ben Farmer; Masakazu Shiota; Alan D Cherrington
Journal:  Am J Physiol Endocrinol Metab       Date:  2009-05-26       Impact factor: 4.310

5.  Liver, but not muscle, has an entrainable metabolic memory.

Authors:  Sheng-Song Chen; Yolanda F Otero; Kimberly X Mulligan; Tammy M Lundblad; Phillip E Williams; Owen P McGuinness
Journal:  PLoS One       Date:  2014-01-23       Impact factor: 3.240

6.  Liver but not adipose tissue is responsive to the pattern of enteral feeding.

Authors:  Yolanda F Otero; Tammy M Lundblad; Eric A Ford; Lawrence M House; Owen P McGuinness
Journal:  Physiol Rep       Date:  2014-02-25
  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.