Original Article
Copyright ©2012 Baishideng Publishing Group Co., Limited. All rights reserved.
World J Gastroenterol. Sep 21, 2012; 18(35): 4875-4884
Published online Sep 21, 2012. doi: 10.3748/wjg.v18.i35.4875
Effect of Tangweian Jianji on upper gastrointestinal remodeling in streptozotocin-induced diabetic rats
Gui-Fang Liu, Jing-Bo Zhao, Zhong Zhen, Hong Sha, Peng-Min Chen, Min Li, Jia-Cheng Zhang, Ming-Ze Yuan, Wen Gao, Hans Gregersen, Xiao-Lin Tong
Gui-Fang Liu, Zhong Zhen, Min Li, Jia-Cheng Zhang, Ming-Ze Yuan, Xiao-Lin Tong, Guang’anmen Hospital, China Academy of Chinese Medical Sciences, Beijing 100053, China
Jing-Bo Zhao, Aalborg Hospital, DK 9000 Aalborg, and Institute of Clinical Medicine, Aarhus University, DK8200 Aarhus N, Denmark
Hong Sha, Peng-Min Chen, Institute of Clinical Medicine, China-Japan Friendship Hospital, Beijing 100029, China
Wen Gao, China Pharmaceutical University, Nanjing 211198, Jiangsu Province, China
Hans Gregersen, Sino-Danish Centre for Education and Research, DK-8000 Aarhus C, Denmark
Author contributions: Tong XL and Gregersen H contributed equally to this work; Tong XL, Gregersen H, Liu GF and Zhao JB designed the research; Liu GF, Sha H, Yuan MZ and Zhang JC performed the experiment; Chen PM and Zhen Z contributed new analytic tools; Li M performed the molecular biology detection; Gao W performed the pharmaceutical detection; Liu GF and Zhao JB analyzed the data; Liu GF and Zhao JB wrote the manuscript; Gregersen H revised the manuscript.
Supported by National Natural Science Foundation of China, No. 81173259/H2708
Correspondence to: Xiao-Lin Tong, Professor of Medicine, Guang’anmen Hospital, China Academy of Chinese Medical Sciences, No. 5 Beixiange St., Xuanwu District, Beijing 100053, China. xiaolintong66@sina.com
Telephone: +86-10-88001260 Fax: +86-10-88001166
Received: February 23, 2012
Revised: April 23, 2012
Accepted: April 27, 2012
Published online: September 21, 2012
Abstract

AIM: To investigate the effect of Tangweian Jianji (TWAJJ) on the biomechanical and morphometrical remodeling of the upper gastrointestinal tract in diabetic rats.

METHODS: Diabetes was induced in 27 rats by injecting streptozotocin (40 mg/kg body weight), the animals were then divided into three groups (n = 9 in each group), i.e., diabetic control (DM); high dose (10 g/kg, T1) and low dose (5 g/kg, T2). Another 10 rats acted as normal controls (Control). TWAJJ was administered by gavage once daily. Blood glucose and serum insulin levels were measured. Circumferential length, wall thickness and opening angle were measured from esophageal, duodenal, jejunal and ileal ring segments. The residual strain was calculated from the morphometric data. Step-wise distension was carried out on esophageal and jejunal segments. The obtained data on the length, diameter and pressure changes were then used to calculate the circumferential and longitudinal stresses and strains. Real-time reverse transcription polymerase chain reaction was used to detect the receptor of advanced glycation end-products (RAGE) mRNA level in jejunal tissues.

RESULTS: At the end of the experiment, the blood glucose level was significantly higher and the serum insulin level was significantly lower in DM, T1 and T2 groups than in the control group (Glucose: 30.23 ± 0.41 mmol/L, 27.48 ± 0.27 mmol/L and 27.84 ± 0.29 mmol/L vs 5.05 ± 0.04 mmol/L, P = 1.65 × 10-16, P = 5.89 × 10-19 and P = 1.63 × 10-18, respectively; Insulin: 1.47 ± 0.32 μg/L, 2.66 ± 0.44 μg/L, 2.03 ± 0.29 μg/L and 4.17 ± 0.54 μg/L, P = 0.0001, P = 0.029 and P = 0.025, respectively). However, these levels did not differ among the DM, T1 and T2 groups. The wet weight per unit length, wall thickness and opening angle of esophageal and intestinal segments in the DM group were significantly higher than those in the control group (from P = 0.009 to P = 0.004). These parameters in the T1 group were significantly lower than those in the DM group (wet weight, duodenum: 0.147 ± 0.003 g/cm vs 0.158 ± 0.001 g/cm, P = 0.047; jejunum, 0.127 ± 0.003 g/cm vs 0.151 ± 0.002 g/cm, P = 0.017; ileum, 0.127 ± 0.004 g/cm vs 0.139 ± 0.003 g/cm, P = 0.046; wall thickness, esophagus: 0.84 ± 0.03 mm vs 0.94 ± 0.02 mm, P = 0.014; duodenum: 1.27 ± 0.06 mm vs 1.39 ± 0.05 mm, P = 0.031; jejunum: 1.19 ± 0.07 mm vs 1.34 ± 0.04 mm, P = 0.047; ileum: 1.09 ± 0.04 mm vs 1.15 ± 0.03 mm, P = 0.049; opening angle, esophagus: 112.2 ± 13.2˚ vs 134.7 ± 14.7˚, P = 0.027; duodenum: 105.9 ± 12.3˚ vs 123.1 ± 13.1˚, P = 0.046; jejunum: 90.1 ± 15.4˚ vs 115.5 ± 13.3˚, P = 0.044; ileum: 112.9 ± 13.4˚ vs 136.1 ± 17.1˚, P = 0.035). In the esophageal and jejunal segments, the inner residual stain was significantly smaller and the outer residual strain was larger in the DM group than in the control group (P = 0.022 and P = 0.035). T1 treatment significantly restored this biomechanical alteration (P = 0.011 and P = 0.019), but T2 treatment did not. Furthermore, the circumferential and longitudinal stiffness of the esophageal and jejunal wall increased in the DM group compared with those in the control group. T1, but not T2 treatment, significantly decreased the circumferential wall stiffness in the jejunal segment (P = 0.012) and longitudinal wall stiffness in the esophageal segment (P = 0.023). The mRNA level of RAGE was significantly decreased in the T1 group compared to that in the DM group (P = 0.0069).

CONCLUSION: TWAJJ (high dose) treatment partly restored the morphometric and biomechanical remodeling of the upper gastrointestinal tract in diabetic rats.

Keywords: Biomechanics and morphometric remodeling; Diabetes rats; Gastrointestinal tract; Mechanism; Tangweian Jianji