Abstract:Objective To investigate the influences of glucagon-like peptide-2(GLP-2)on intestinal mucosal immune barrier in mice with sever acute pancreatitis(SAP).Methods All healthy female BALB/C mice were divided into normal control, SAP and GLP-2 group by random allocation. SAP mice model was established by intraperitoneal injections with large dose L-Arg. The changes of CD3+, CD4+, CD8+ lymphocyte and IgA λ chain of intestinal mucous membrane and amylase of blood and ascites were observed. The same method was used in GLP-2 group to observe the changes of the above indices.Results The blood and ascites amylase value in SAP groups were (1 260.93±58.99)U/L and (389.33±30.31)U/L respectively, were significantly higher than those in NC group and GLP-2 treatment group (all P values<0.01). Expression of SAP in intestinal mucosa of mice CD3+, CD4+, CD8+ lymphocytes and IgA λ chain were (19.57±6.56)/HP,(5.49±2.97)/HP,(2.96±1.22)/HP and (6.20±3.22)/HP respectively, were obviously higher than those of the NC group and the SAP group(all P values<0.05). Compared with the NC group, expression of mice CD4+ lymphocytes and IgAλ chain of GLP-2 treatment group had no statistical significance (all P values>0.05).Conclusions GLP-2 can increase the expression of CD3+, CD4+, CD8+ lymphocytes and IgA λ chain in intestinal mucosa of SAP mice, and has the protective effect on intestinal immune barrier.
孙凡华,许建国,张宗兵,孔令尚,汪华学,刘牧林,程兴望,何先弟. 胰高血糖素样肽-2对急性胰腺炎小鼠肠黏膜免疫屏障的影响[J]. 中华解剖与临床杂志, 2014, 19(4): 316-319.
Sun Fanhua , Xu Jianguo, Zhang Zongbing, Kong Lingshang, Wang Huaxue, Liu Mulin, Cheng Xingwang, He Xiandi. Effect of glucagon-like peptide-2 on intestinal mucosal immune barrier in mice with acute pancreatitis. Chinese Journal of Anatomy and Clinics, 2014, 19(4): 316-319.
Zhang XP, Jiang J, Cheng QH, et al. Protective effects of ligustrazine, kakonein and panax notoginsenoside on the small intestine and immune organs of rats with severe acute pancreatitis[J]. Hepatobiliary Pancreat Dis Int, 2011,10(6):632- 637.
[2]
Mizunuma T, Kawamura S, Kishino Y. Effects of injecting excess arginine on rat pancreas[J]. J Nutr ,1984, 114(3): 467- 471.
[3]
Sun JK, Mu XW, Li WQ, et al. Effects of early enteral nutrition on immune function of severe acute pancreatitis patients[J]. World J Gastroenterol, 2013, 19(6):917- 22.
[4]
Zou XP, Chen M, Wei W, et al. Effects of enteral immunonutrition on the maintenance of gut barrier function and immune function in pigs with severe acute pancreatitis[J]. JPEN J Parenter Enteral Nutr, 2010,34(5):554- 566.
[5]
Durcker DJ, Ehrlich P, Asa SL, et al. Induction of intestinal epithelial proliferation by glucagons- like peptide 2[J]. Proc Natl Acad Sci USA,1996, 93(15): 7911- 7916.
[6]
Wang JH, Inoue T, Higashiyama M,et al. Umami receptor activation increases duodenal bicarbonate secretion via glucagon- like peptide- 2 release in rats[J]. J Pharmacol Exp Ther,2011, 339(2): 464- 734.
[7]
Kissow H, Hartmann B, Holst JJ,et al. Glucagon- like peptide- 1 as a treatment for chemotherapy- induced mucositis[J]. Gut, 2013, 62(12):1724- 1733.
Rowland KJ, Brubaker PL. Life in the crypt: a role for glucagon- like peptide- 2 [J].Mol Cell Endocrinol, 2008, 288(1- 2):63- 70.
[10]
Yusta B, Holland D, Waschek JA, et al. Intestinotrophic glucagon-like peptide-2 (GLP-2) activates intestinal gene expression and growth factor-dependent pathways independent of the vasoactive intestinal peptide gene in mice[J]. Endocrinology, 2012, 153(6):2623- 2632.
[11]
Bvemholm L, Hornum M, Henriksen BM, et al. Glucagon-like peptide-2 increases mesenteric blood flow in humans[J].Scand J Gastroenterol, 2009, 44(3): 314- 319.
[12]
Hsieh J, Longuet C, Maida A, et al. Glucagon-like peptide-2 increases intestinal lipid absorption and chylomicron production via CD36[J]. Gastroenterology, 2009,137(3): 997- 1005.