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Published in: BMC Complementary Medicine and Therapies 1/2015

Open Access 01-12-2015 | Research article

Suppression of acute pancreatitis by L-lysine in mice

Author: Abdulrahman L. Al-Malki

Published in: BMC Complementary Medicine and Therapies | Issue 1/2015

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Abstract

Background

Acute pancreatitis is an inflammatory disease caused by several factors such as viral infection, drugs, and diagnostic endoscopy. The aim of this study was to evaluate the potential protective or therapeutic effects of L-lysine on pancreatitis induced by L-arginine in mice.

Methods

Four groups of mice (10 in each group) were assessed. Group I was the control. Animals in groups II–IV were injected intraperitoneally with L-arginine hydrochloride (400 mg/kg body weight [bw]) for 3 days. Group III animals were orally pre-treated with L-lysine (10 mg/kg bw), whereas group IV animals were orally post-treated with L-lysine (10 mg/kg bw). Serum samples were subjected to amylase, lipase, transaminase, and interleukin-6 (IL-6) assays. The pancreas was excised to measure the levels of malondialdehyde, nitric oxide, catalase, superoxide dismutase, reduced glutathione, and glutathione peroxidase.

Results

Pre- or post-treatment with L-lysine led to significant decreases in the levels of malondialdehyde and nitric oxide, while significant enhancement was observed in the activities of antioxidant enzymes (superoxide dismutase, catalase, and glutathione peroxidase) and glutathione (p < 0.001). However, the treatment potential of L-lysine was better as a protective agent than a therapeutic agent.

Conclusions

L-lysine treatment attenuates pancreatic tissue injury induced by L-arginine by inhibiting the release of the inflammatory cytokine IL-6 and enhance antioxidant activity. These effects may involve upregulation of anti-inflammatory factors and subsequent downregulation of IL6.
Literature
1.
go back to reference Reila A, Zeinthmeister AR, Milton Lj. Etiology, incidence and survival of acute pancreatitis in olmested county, Minnosota. Gastroentrology 1991. p. 100-A269 Reila A, Zeinthmeister AR, Milton Lj. Etiology, incidence and survival of acute pancreatitis in olmested county, Minnosota. Gastroentrology 1991. p. 100-A269
2.
go back to reference Banerjee AK, Galloway SW, Kingsnorth AN. Experimental models of acute pancreatitis. Br J Surg. 1994;81:1093–106.CrossRef Banerjee AK, Galloway SW, Kingsnorth AN. Experimental models of acute pancreatitis. Br J Surg. 1994;81:1093–106.CrossRef
3.
go back to reference Formela LJ, Galloway SW, Kingsnorth AN. Inflamatory mediators in acute pancreatitis. Br J Surg. 1995;82:6–13.CrossRefPubMed Formela LJ, Galloway SW, Kingsnorth AN. Inflamatory mediators in acute pancreatitis. Br J Surg. 1995;82:6–13.CrossRefPubMed
4.
go back to reference Acosta JM, Ledesma CL. Gallstone migration as a cause of acute pancreatitis. N Engl J Med. 1974;290:484–7.CrossRefPubMed Acosta JM, Ledesma CL. Gallstone migration as a cause of acute pancreatitis. N Engl J Med. 1974;290:484–7.CrossRefPubMed
5.
go back to reference Kelly TR. Gallstone pancreatitis: the timing of surgery. Surgery. 1980;88:345–50.PubMed Kelly TR. Gallstone pancreatitis: the timing of surgery. Surgery. 1980;88:345–50.PubMed
6.
go back to reference Moody FG, Senninger N, Runkel N. Another challenge to the Opie’s theory. Gastroenterology. 1993;104:927–31.CrossRefPubMed Moody FG, Senninger N, Runkel N. Another challenge to the Opie’s theory. Gastroenterology. 1993;104:927–31.CrossRefPubMed
7.
go back to reference Crunkel N, Moody F, Mueller W. Experimental evidence against Opie’s common channel bile reflux theory. Digestion. 1992;52:67–7. Crunkel N, Moody F, Mueller W. Experimental evidence against Opie’s common channel bile reflux theory. Digestion. 1992;52:67–7.
8.
go back to reference Baris D, Yildiz EH. Basic Experimental Pancreatitis Models for Beginners. Surg Sci. 2010;1:31–9.CrossRef Baris D, Yildiz EH. Basic Experimental Pancreatitis Models for Beginners. Surg Sci. 2010;1:31–9.CrossRef
9.
go back to reference Smotkin J, Tenner S. Laboratory diagnostic tests in acute pancreatitis. J Clin Gastroenterol. 2002;34:459–62.CrossRefPubMed Smotkin J, Tenner S. Laboratory diagnostic tests in acute pancreatitis. J Clin Gastroenterol. 2002;34:459–62.CrossRefPubMed
10.
go back to reference Tani S, Itoh H, Okabayashi Y, Nakamura T, Fuji M, Fujisawa T, et al. New model of acute necrotizing pancreatitis induced by excessive doses of arginine in rats. Dig Dis Sci. 1990;35:367–74.CrossRefPubMed Tani S, Itoh H, Okabayashi Y, Nakamura T, Fuji M, Fujisawa T, et al. New model of acute necrotizing pancreatitis induced by excessive doses of arginine in rats. Dig Dis Sci. 1990;35:367–74.CrossRefPubMed
11.
go back to reference SU KH, Cuthbertson C, Christophi C. Review of experimental animal models of acute pancreatitis. HPB. 2006;8:264–86.CrossRefPubMed SU KH, Cuthbertson C, Christophi C. Review of experimental animal models of acute pancreatitis. HPB. 2006;8:264–86.CrossRefPubMed
12.
go back to reference Hegyi P, Rakonczay Jr Z, Sári R, Góg C, Lonovics J, Takács T, et al. L-arginine-induced experimental pancreatitis. World J Gastroenterol. 2004;10:2003–9.CrossRefPubMedPubMedCentral Hegyi P, Rakonczay Jr Z, Sári R, Góg C, Lonovics J, Takács T, et al. L-arginine-induced experimental pancreatitis. World J Gastroenterol. 2004;10:2003–9.CrossRefPubMedPubMedCentral
13.
go back to reference Shimomura A, Matsui I, Hamano T, Ishimoto T, Katou Y, Takehana K, et al. Dietary L-lysine prevents arterial calcification in adenine-induced uremic rats. J Am Soc Nephrol. 2014;25(9):1954–65.CrossRefPubMedPubMedCentral Shimomura A, Matsui I, Hamano T, Ishimoto T, Katou Y, Takehana K, et al. Dietary L-lysine prevents arterial calcification in adenine-induced uremic rats. J Am Soc Nephrol. 2014;25(9):1954–65.CrossRefPubMedPubMedCentral
14.
go back to reference Griffith RS, DeLong DC, Nelson JD. Relation of arginine-lysine antagonism to Herpes simplex growth in tissue culture. Chemotherapy. 1981;27:209–13.CrossRefPubMed Griffith RS, DeLong DC, Nelson JD. Relation of arginine-lysine antagonism to Herpes simplex growth in tissue culture. Chemotherapy. 1981;27:209–13.CrossRefPubMed
15.
go back to reference Yagi K, Rastogi R. Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction. Anal Biochem. 1979;95:351–8.CrossRefPubMed Yagi K, Rastogi R. Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction. Anal Biochem. 1979;95:351–8.CrossRefPubMed
16.
go back to reference Green LC, Wagner DA, Glogowski J, et al. Analysis of nitrate, nitrite, and [15 N] nitrate in biological fluids. Anal Biochem. 1982;126:131–8.CrossRefPubMed Green LC, Wagner DA, Glogowski J, et al. Analysis of nitrate, nitrite, and [15 N] nitrate in biological fluids. Anal Biochem. 1982;126:131–8.CrossRefPubMed
17.
go back to reference Kakkar P, Das B, Visvanathan PN. A modified spectrophotometric assay of superoxide dismutase. Ind J Biochem. 1972;197:588–90. Kakkar P, Das B, Visvanathan PN. A modified spectrophotometric assay of superoxide dismutase. Ind J Biochem. 1972;197:588–90.
18.
go back to reference Valentine WN, Pagila DE. Studies in the glutathione characterization of erythrocyte. J Lab Clin Med. 1967;1967(70):158–69. Valentine WN, Pagila DE. Studies in the glutathione characterization of erythrocyte. J Lab Clin Med. 1967;1967(70):158–69.
19.
go back to reference Moran MS. Levels of glutathione, glutathione reductase and glutathione-S-transferase activity in rat lung and liver. Biochim et Biophys. 1979;582:67–78.CrossRef Moran MS. Levels of glutathione, glutathione reductase and glutathione-S-transferase activity in rat lung and liver. Biochim et Biophys. 1979;582:67–78.CrossRef
20.
go back to reference Aebi H. Catalase: In Method of enzymatic analysis. HU Bergmeyer, edition, New york: Weinheim Verlag Chemie Academic Press; 1974;673–685. Aebi H. Catalase: In Method of enzymatic analysis. HU Bergmeyer, edition, New york: Weinheim Verlag Chemie Academic Press; 1974;673–685.
21.
go back to reference Habig WH, Pabst MJ, Jacoby WBC. Glutathione-Stransferase: The first enzymatic step in mercapturic acid formation. J Biol Chem. 1974;249:7130–9.PubMed Habig WH, Pabst MJ, Jacoby WBC. Glutathione-Stransferase: The first enzymatic step in mercapturic acid formation. J Biol Chem. 1974;249:7130–9.PubMed
22.
go back to reference Niederau C, Ferrell LD, Grendell JH. Caerulein-induced acute necrotizing pancreatitis in mice: Protective effects of proglumide, benzotript, and secretin. Gastroenterology. 1985;88:1192–204.CrossRefPubMed Niederau C, Ferrell LD, Grendell JH. Caerulein-induced acute necrotizing pancreatitis in mice: Protective effects of proglumide, benzotript, and secretin. Gastroenterology. 1985;88:1192–204.CrossRefPubMed
23.
go back to reference Lechin F, van der Dijs B. Arginine–induced pancreatitis: involvement of the autonomic nervous system? Am J Physiol Gastrointest Liver Physiol. 2008;294:G1450–1.CrossRefPubMed Lechin F, van der Dijs B. Arginine–induced pancreatitis: involvement of the autonomic nervous system? Am J Physiol Gastrointest Liver Physiol. 2008;294:G1450–1.CrossRefPubMed
24.
go back to reference Schmidt J, Lewandrowsi K, Warshaw AL, Compton CC, Rattner DW. Morphometric characteristics and homogeneity of a new model of acute pancreatitis in the rat. Int J Pancreatol. 1992;12:41–51.PubMed Schmidt J, Lewandrowsi K, Warshaw AL, Compton CC, Rattner DW. Morphometric characteristics and homogeneity of a new model of acute pancreatitis in the rat. Int J Pancreatol. 1992;12:41–51.PubMed
25.
go back to reference Ding S-P, Li J-C, Jin C. A mouse model of severe acute pancreatitis induced with caerulein and lipopolysaccharide. World J Gastroenterol. 2003;9(3):584–9.CrossRefPubMedPubMedCentral Ding S-P, Li J-C, Jin C. A mouse model of severe acute pancreatitis induced with caerulein and lipopolysaccharide. World J Gastroenterol. 2003;9(3):584–9.CrossRefPubMedPubMedCentral
Metadata
Title
Suppression of acute pancreatitis by L-lysine in mice
Author
Abdulrahman L. Al-Malki
Publication date
01-12-2015
Publisher
BioMed Central
Published in
BMC Complementary Medicine and Therapies / Issue 1/2015
Electronic ISSN: 2662-7671
DOI
https://doi.org/10.1186/s12906-015-0729-x

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