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Copyright ©The Author(s) 2003. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastroenterol. Aug 15, 2003; 9(8): 1874-1877
Published online Aug 15, 2003. doi: 10.3748/wjg.v9.i8.1874
Effects of neurotrophins on gastrointestinal myoelectric activities of rats
Ning-Li Chai, Lei Dong, Zong-Fang Li, Ke-Xin Du, Jian-Hua Wang, Li-Kun Yan, Xi-Lin Dong
Ning-Li Chai, Lei Dong, Xi-Lin Dong, Department of Digestion, Second Affiliated Hospital, Xi’an Jiaotong University, Xi’an 710004, Shaanxi Province, China
Zong-Fang Li, Department of General Surgery, Second Affiliated Hospital, Xi’an Jiaotong University, Xi’an 710004, Shaanxi Province, China
Ke-Xin Du, Functional Center of Medical School, Xi’an Jiaotong University, Xi’an 710061, Shaanxi Province, China
Jian-Hua Wang, Li-Kun Yan, Department of General Surgery, Shaanxi Provincial People’s Hospital, Xi’an 710068, Shaanxi Province, China
Author contributions: All authors contributed equally to the work.
Supported by the National Natural Science Foundation of China, No. 30170414
Correspondence to: Lei Dong, Department of Digestion, Second Affiliated Hospital, Xi’an Jiaotong University, Xi’an 710004, Shaanxi Province, China. csxlily@ hotmail.com
Telephone: +86-29-8024005 Fax: +86-29-7231758
Received: January 18, 2003
Revised: January 26, 2003
Accepted: March 10, 2003
Published online: August 15, 2003
Abstract

AIM: To observe the effects of mouse nerve growth factor (NGF), rat recombinant brain derived neurotrophic factor (rm-BDNF) and recombinant human neurotrophin-3 (rh-NT-3) on the gastrointestinal motility and the migrating myoelectric complex (MMC) in rat.

METHODS: A randomized, double-blinded, placebo-controlled experiment was performed. 5-7 days after we chronically implanted four or five bipolar silver electrodes on the stomach, duodenum, jejunum and colon, 21 experimental rats were coded and divided into 3 groups and injected NGF, rm-BDNF, rh-NT-3 or placebo respectively via tail vein at a dose of 20 μg·kg- 1. The gastrointestinal myoelectrical activity was recorded 2 hours before and after the test substance infusions in these consciously fasting rats.

RESULTS: The neurotrophins-induced pattern of activity was characterized by enhanced spiking activity of different amplitudes at all recording sites, especially in the colon. In the gastric antrum and intestine, only rh-NT-3 had increased effects on the demographic characteristics of electrical activities (P < 0.05), but did not affect the intervals of MMCs. In the colon, all the three kinds of neurotrophins could significantly increase the frequency, amplitude and duration levels of spike bursts, and also rh-NT-3 could prolong the intervals of MMC in the transverse colon (25 ± 11 min vs 19 ± 6 min, P < 0.05). In the distal colon rh-NT-3 could evoke phase III-like activity and disrupt the MMC pattern, which was replaced by a continuously long spike bursts (LSB) and irregular spike activity (ISA) for 48 ± 6 min.

CONCLUSION: Exogenous neurotrophic factors can stimulate gut myoelectric activities in rats.

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