Horm Metab Res 2011; 43(6): 369-373
DOI: 10.1055/s-0031-1277155
Original Basic

© Georg Thieme Verlag KG Stuttgart · New York

Involvement of Nitric Oxide in Corticosterone Release and Glucose Metabolism in Food Deprived Rats

B. Mornagui1 , R. Rezg1 , A. Grissa1 , C. Gharib2 , A. Kamoun1 , S. El-Fazaa1 , N. Gharbi1
  • 1Laboratoire de Physiologie des Agressions, Faculté des Sciences de Tunis, El Manar, Tunisia
  • 2Laboratoire de Physiologie de l’Environnement, Faculté de Médecine Grange-Blanche, Lyon, France
Further Information

Publication History

received 04.10.2010

accepted 05.04.2011

Publication Date:
09 May 2011 (online)

Abstract

This study was performed to investigate the involvement of nitric oxide (NO) in corticosterone, endpoint product of hypothalamo-pituitary-adrenal (HPA) axis activation, and metabolic responses to 3 days of food deprivation. To investigate this aim, we used a nonspecific inhibitor of nitric oxide synthases, N-nitro-L-arginine methyl ester (L-NAME). In food deprived group we have noted a significant increase in plasma corticosterone concentration accompanied by a significant depletion in hepatic glycogen content with concomitant increase in glycogen phosphorylase (GP) activity by 63.72%, key enzyme of glycogenolysis and decrease in hexokinase (HK) activity by 25.16%, leading to significant decrease in glucose concentration. However, L-NAME administration in food deprived rats decreased slightly corticosterone level and GP activity (16.39%) and increased HK activity (11.26%) as compared to food deprived group. Considering these results, we can deduce that in food deprivation nitric oxide is involved in the regulation of corticosterone release and in glucose metabolic responses via glycogenolysis activation by the stimulation of GP activity and the inhibition of HK activity. However, more studies are necessary to further clarify the mechanisms by which NO induces these responses.

References

  • 1 Koretz RL. Should patients with cancer be offered nutritional support: does the benefit outweigh the burden?.  Eur J Gastroenterol Hepatol. 2007;  19 379-382
  • 2 Beishuizen A, Thijs LG. Endotoxin and the hypothalamo-pituitary-adrenal (HPA) axis.  J Endotoxin Res. 2003;  9 3-24
  • 3 Givalois L, Naert G, Rage F, Ixart G, Arancibia S, Tapia-Arancibia L. A single brain-derived neurotrophic factor injection modifies hypothalamo-pituitary-adrenocortical axis activity in adult male rats.  Mol Cell Neurosci. 2004;  27 280-295
  • 4 Rezg R, Mornagui B, El-Arbi M, Kamoun A, El-Fazaa S, Gharbi N. Effect of subchronic exposure to malathion on glycogen phosphorylase and hexokinase activities in rat liver using native PAGE.  Toxicology. 2006;  223 9-14
  • 5 Schmidt HH, Walter U. NO at work.  Cell. 1994;  78 919-925
  • 6 Raber J, Koob GF, Bloom FE. Interleukin-2 (IL-2) induces corticotropin-releasing factor (CRF) release from the amygdala and involves a nitric oxide-mediated signaling; comparison with the hypothalamic response.  J Pharmacol Exp Ther. 1995;  272 815-824
  • 7 Akasaka S, Nomura M, Nishii H, Fujimoto N, Ueta Y, Tsutsui M, Shimokawa H, Yanagihara N, Matsumoto T. The hypothalamo-pituitary axis responses to lipopolysaccharide-induced endotoxemia in mice lacking inducible nitric oxide synthase.  Brain Res. 2006;  1089 1-9
  • 8 Adams ML, Nock B, Truong R, Cicero TJ. Nitric oxide control of steroidogenesis: endocrine effects of NG-nitro-L-arginine and comparisons to alcohol.  Life Sci. 1992;  50 PL35-PL40
  • 9 Jobgen WS, Fried SK, Fu WJ, Meininger CJ, Wu G. Regulatory role for the arginine-nitric oxide pathway in metabolism of energy substrates.  J Nutr Biochem. 2006;  17 571-588
  • 10 Sugita H, Kaneki M, Tokunaga E, Sugita M, Koike C, Yasuhara S, Tompkins RG, Martyn JA. Inducible nitric oxide synthase plays a role in LPS-induced hyperglycemia and insulin resistance.  Am J Physiol Endocrinol Metab. 2002;  282 E386-E394
  • 11 Stadler J, Barton D, Beil-Moeller H, Diekmann S, Hierholzer C, Erhard W, Heidecke CD. Hepatocyte nitric oxide biosynthesis inhibits glucose output and competes with urea synthesis for L-arginine.  Am J Physiol. 1995;  268 G183-G188
  • 12 Borgs M, Bollen M, Keppens S, Yap SH, Stalmans W, Vanstapel F. Modulation of basal hepatic glycogenolysis by nitric oxide.  Hepatology. 1996;  23 1564-1571
  • 13 Sprangers F, Sauerwein HP, Romijn JA, van Woerkom GM, Meijer AJ. Nitric oxide inhibits glycogen synthesis in isolated rat hepatocytes.  Biochem J. 1998;  330 (Pt 2) 1045-1049
  • 14 Mornagui B, Grissa A, Duvareille M, Gharib C, Kamoun A, El-Fazaa S, Gharbi N. Vasopressin and nitric oxide synthesis after three days of water or food deprivation.  Acta Biol Hung. 2006;  57 1-11
  • 15 Kamiya A, Iwase S, Michikami D, Fu Q, Mano T, Kitaichi K, Takagi K. Increased vasomotor sympathetic nerve activity and decreased plasma nitric oxide release after head-down bed rest in humans: disappearance of correlation between vasoconstrictor and vasodilator.  Neurosci Lett. 2000;  281 21-24
  • 16 Tracey WR, Tse J, Carter G. Lipopolysaccharide-induced changes in plasma nitrite and nitrate concentrations in rats and mice: pharmacological evaluation of nitric oxide synthase inhibitors.  J Pharmacol Exp Ther. 1995;  272 1011-1015
  • 17 Lott JA, Turner K. Evaluation of Trinder's glucose oxidase method for measuring glucose in serum and urine.  Clin Chem. 1975;  21 1754-1760
  • 18 Good CA, Krames H, Somogyi M. Method in enzymology VII. Chemical procedures for analysis of polysaccharides.. New York: Academic Press; 1933
  • 19 Pasteur N, Pasteur GBF, Catalon J, Britton-Davidion J. Manuel technique de génétique par électrophorèse des Protéines.  1987;  57
  • 20 Bradford MM. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding.  Anal Biochem. 1976;  72 248-254
  • 21 Gennady M. ed Handbook of detection of enzymes on electrophoretic gels.. CRC Press; 1994: 112-135
  • 22 Schwartz MW, Dallman MF, Woods SC. Hypothalamic response to starvation: implications for the study of wasting disorders.  Am J Physiol. 1995;  269 R949-R957
  • 23 Dallman MF, Strack AM, Akana SF, Bradbury MJ, Hanson ES, Scribner KA, Smith M. Feast and famine: critical role of glucocorticoids with insulin in daily energy flow.  Front Neuroendocrinol. 1993;  14 303-347
  • 24 Dallman MF, Akana SF, Bhatnagar S, Bell ME, Choi S, Chu A, Horsley C, Levin N, Meijer O, Soriano LR, Strack AM, Viau V. Starvation: early signals, sensors, and sequelae.  Endocrinology. 1999;  140 4015-4023
  • 25 Lopez-Figueroa MO, Day HE, Akil H, Watson SJ. Nitric oxide in the stress axis.  Histol Histopathol. 1998;  13 1243-1252
  • 26 Rettori V, Fernandez-Solari J, Mohn C, Zorrilla Zubilete MA, de la Cal C, Prestifilippo JP, De Laurentiis A. Nitric oxide at the crossroad of immunoneuroendocrine interactions.  Ann NY Acad Sci. 2009;  1153 35-47
  • 27 Mohn CE, Fernandez-Solari J, De Laurentiis A, Prestifilippo JP, de la Cal C, Funk R, Bornstein SR, McCann SM, Rettori V. The rapid release of corticosterone from the adrenal induced by ACTH is mediated by nitric oxide acting by prostaglandin E2.  Proc Natl Acad Sci U S A. 2005;  102 6213-6218
  • 28 Vila R, Adan C, Grasa MM, Masanes RM, Esteve M, Cabot C, Fernandez-Lopez JA, Remesar X, Alemany M. Effect of food deprivation on rat plasma estrone fatty acid esters.  Diabetes Obes Metab. 1999;  1 353-356
  • 29 Reshef L, Olswang Y, Cassuto H, Blum B, Croniger CM, Kalhan SC, Tilghman SM, Hanson RW. Glyceroneogenesis and the triglyceride/fatty acid cycle.  J Biol Chem. 2003;  278 30413-30416
  • 30 Finn PF, Dice JF. Proteolytic and lipolytic responses to starvation.  Nutrition. 2006;  22 830-844
  • 31 Taylor AW, Cary S, McNulty M, Garrod J, Secord DC. Effects of food restriction and exercise upon the deposition and mobilization of energy stores in the rat.  J Nutr. 1974;  104 218-222
  • 32 Farghali H, Hodis J, Kutinova-Canova N, Potmesil P, Kmonickova E, Zidek Z. Glucose release as a response to glucagon in rat hepatocyte culture: involvement of NO signaling.  Physiol Res. 2008;  57 569-575
  • 33 Bornstein SR, Chrousos GP. Clinical review 104: Adrenocorticotropin (ACTH)- and non-ACTH-mediated regulation of the adrenal cortex: neural and immune inputs.  J Clin Endocrinol Metab. 1999;  84 1729-1736
  • 34 Di Giulio RT, Scanlon PF. Effects of cadmium ingestion and food restriction on energy metabolism and tissue metal concentrations in mallard ducks (Anas platyrhynchos).  Environ Res. 1985;  37 433-444

Correspondence

B. Mornagui

Laboratoire de Physiologie des

Agressions

Département de Biologie

Faculté des Sciences de Tunis

Campus Universitaire

2092 El Manar

Tunisia

Phone: +216/71/872 600

Fax: +216/71/871 666

Email: bessem.mornagui@fst.rnu.tn

    >