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Dong-Ping
Xie, Lian-Bi Chen, Department of Physiology, Medical College,
Shandong University, Jinan 250012, Shandong Province, China
Wei Li, Song-Yi Qu, Tian-Zhen Zheng, Department of
Physiology, Lanzhou Medical College, Lanzhou 730000,Gansu Province,
China
Ying-Li Yang, Northwest Normal University,Lanzhou 730070,
Gansu Province, China
Yong-Hui Ding, Yu-Ling Wei, Drug Control Institute of Gansu
Province, Lanzhou 730000,Gansu Province, China
Supported by the Natural Scientific Foundation of Shandong
Province, No.Y2001C06
Correspondence to: Dong-Ping Xie, Department of Physiology,
Medical College, Shandong University, Jinan 250012, Shandong
Province, China. xiedping@sdu.edu.cn
Telephone: +86-531-2942037 Fax: +86-531-2942156
Received 2001-07-19 Accepted 2002-01-20
Abstract
AIM: To
investigate the effects of areca on the contractile activity of
isolated colonic muscle strips in rats and mechanism involved.
METHODS:
Each
strip (LMPC, longitudinal muscle of proximal colon; CMPC, circular
muscle of proximal colon; LMDC, longitudinal muscle of distal colon;
CMDC, circular muscle of distal colon.) was suspended in a tissue
chamber containing 5mL Krebs solution (37℃),
bubbled continuously with 950mL·L-1 O2 and
50mL·L-1 CO2. The mean contractile amplitude
(A), the resting tension (T), and the contractile frequency (F) were
simultaneously recorded on recorders.
RESULTS:
Areca
dose dependently increased the mean contractile amplitude, the
resting tension of proximal and distal colonic smooth muscle strips
in rats (P<0.05). It also partly increased the contractile
frequency of colonic smooth muscle strips in rats (P<0.05).
The effects were partly inhibited by atropine (the resting tension
of LMPC decreased from 0.44±0.12 to 0.17±0.03; the resting tension
of LMDC decreased from 0.71±0.14 to 0.03±0.01; the mean
contractile amplitude of LMPC increased from -45.8±7.2 to -30.5±2.9;
the motility index of CMDC decreased from 86.6±17.3 to 32.8±9.3; P<0.05
vs areca), but the effects were not inhibited by hexamethonium (P>0.05).
CONCLUSION:
Areca
stimulated the motility of isolated colonic smooth muscle strips in
rats. The stimulation of areca might be relevant with M receptor
partly.
Xie
DP, Li W, Qu SY, Zheng TZ, Yang YL, Ding YH, Wei YL, Chen LB. Effect
of areca on contraction of colonic muscle strips in rats. World J
Gastroenterol 2002;8(2):350-352
INTRODUCTION
Areca ( Areca catechu L. ) had already been shown to relieve
indigestion, unblocked stagnation of the circulation of vital
energy. It had been used to treat abdominal distention and
constipation, which were caused by stagnation of the circulation of
vital energy in taste. But the actions and mechanisms of areca on
the colonic smooth muscle motility are not reported. In this study,
we observed the effect of areca on the different colonic smooth
muscle strips in rats and investigated the mechanism involved.
MATERIALS
AND METHODS
Animal preparation
Wistar rats of either sex (gradeⅠ,
purchased from Animal Center of Lanzhou Medical College), weighing
200-250g, were sacrificed, and the proximal colon and distal colon
were removed[1]. The segments of the colon were opened
along the mesentery. Muscle strips (8×3mm) were cut, parallel to
either the circular or the longitudinal fibers, and named circular
muscle of proximal colon (CMPC), longitudinal muscle of proximal
colon (LMPC), circular muscle of distal colon (CMDC), and
longitudinal muscle of distal colon (LMDC). The mucosa on each strip
was carefully removed.
Experiments
The muscle strip was suspended in a tissue chamber containing 5mL
Krebs solution (37℃)
and bubbled continuously with 950mL·L-1 O2
and 50mL·L-1 CO2[2]. One end of
the strip was fixed to a hook on the bottom of the chamber. The
other end was connected to an external isometric force transducer (JZ-BK,BK).
Motility of colonic strips (under an initial tension of 1g) in 4
tissue chambers were simultaneously recorded on ink-writing
recorders (LMS-ZB, Cheng-Du). After 1h equilibration,
areca(10,100,1000g·L-1 ) was added in the tissue chamber
to observe their effects on colon; atropine(0.01μmol·L-1
) or hexamethonium(10μmol·L-1 ), given 3min before
the administration of areca(100g·L-1 ), was added
separately to investigate whether the actions of areca were relevant
with M receptor or N receptor. The resting tension, the frequency,
and the mean contractile amplitude of LMPC, CMPC and LMDC, as well
as the motility index of CMDC were measured. Motility index=∑(amplitude×duration).
Drugs
preparation
Areca was broken into pieces, boiled, filtrated, and diluted to
1000g·L-1 (the drug was appraised and prepared by Drug
Control Institute of Gansu Province). The following agents were
used: atropine (Pharmaceutical Factory in Yancheng, Jiangsu
Province), hexamethonium (Sigma Chemical Company).
Data
analysis
The results were presented as mean±SD , and statistically analyzed
by paired t test, P<0.05 was considered to be significant.
RESULTS
Effect of areca on the spontaneous contraction of colonic smooth
muscle strips
Areca (10,100,1000g·L-1 ) dose dependently increased the
mean contractile amplitude of CMPC and LMDC, the motility index of
CMDC, and the resting tension of LMPC, LMDC and CMDC; but it
decreased the mean contractile amplitude of LMPC (Figure 1). It
increased the contractile frequency of CMPC and LMDC (Table 1). It
had no significant effects on the resting tension of CMPC and the
contractile frequency of LMPC and CMDC.
Figure
1(PDF)Effect
of areca on the mean contractile (the motility index of CMDC) and
the resting tension ( mean±SD , n=12) LMPC: longitudinal
muscle of proximal colon; CMPC: circular muscle of proximal colon;
LMDC: longitudinal muscle of distal colon; CMDC: circular muscle of
distal colon. A, the mean contractile amplitude; T, the resting
tension. aP<0.05, bP<0.01 vs
control.
Table
1
Effect of areca on the contractile frequency of colonic contractile
in rats ( mean±SD , waves·min-1 , n=12)
|
|
Areca
(g·L-1)
|
|
0
|
10
|
0
|
100
|
0
|
1000
|
|
LMPC
|
1.8±0.2
|
1.9±0.2
|
2.2±0.2
|
2.5±0.3
|
1.8±0.2
|
1.8±0.4
|
|
CMPC
|
1.5±0.1
|
1.5±0.1
|
1.
6±0.1
|
2.1±0.2a
|
1.6±0.1
|
2.3±0.1b
|
|
LMDC
|
1.3±0.1
|
1.3±0.1
|
1.5±0.1
|
2.3±0.2a
|
1.5±0.2
|
2.7±0.5b
|
|
CMDC
|
0.7±0.1
|
0.7±0.1
|
0.6±0.1
|
0.6±0.1
|
0.6±0.1
|
0.6±0.1
|
LMPC:
longitudinal muscle of proximal colon; CMPC: circular muscle of
proximal colon; LMDC: longitudinal muscle of distal colon; CMDC:
circular muscle of distal colon. aP<0.05, bP<0.01
vs control (0).
Effect
of atropine on the responses caused by areca
Atropine (0.01μmol·L-1 ) itself had no significant
effects on rat colon. But when given 3min before the administration
of areca (100g·L-1), it reduced the increasing action of
areca on the resting tension of LMPC and LMDC, the motility index of
CMDC, and the mean contractile amplitude of LMPC. It had no
significant effects on the other action of areca (Table 2).
Table
2 Effect
of areca on the mean contractile amplitude and the resting tension
of colon, and the motilityindex of distal colon after atropine
pretreatment in rats (mean±SD , n=12)
|
|
LMPC
|
CMPC
|
LMDC
|
CMDC
|
|
T/g
|
A/mm
|
T/g
|
A/mm
|
T/g
|
A/mm
|
T/g
|
MI/mm·s-1
|
|
Areca
|
0.44.±0.12b
|
-45.8±7.2b
|
0
|
40.0±3.5b
|
0.71±0.14b
|
79.7±12.8b
|
0.11±0.05a
|
86.6±17.3b
|
|
Atropine
|
0
|
0.1±0.1
|
0
|
0.6±1.4
|
0
|
1.3±3.0
|
0
|
0.9±1.3
|
|
Atropine+Areca
|
0.17±0.03bc
|
-30.5±2.9
|
0
|
36.9±2.5b
|
0.03±0.01ab
|
70.9±13.6b
|
0.03±0.02
|
32.±98.3bc
|
T,
the resting tension; A, the mean contractile amplitude; MI, the
motility index. aP<0.05, bP<0.001
vs control. cP<0.05, dP<0.001
vs areca.
Effect
of hexamethonium on the responses caused by areca
Hexamethonium (10μmol·L-1 ) had no significant
effect on the contractile activity of each colonic smooth muscle
strip. Hexamethonium given 3 minute before administration of areca
(100g·L-1 ) had no significant effects on the action of
areca.
DISCUSSION
There are many diseases which are caused by colonic motility
disorder or accompany with colonic motility abnormality, such as
constipation, diarrhea, irritable bowel syndrome and so on[3-11].
There are some reports on the study of normal colonic motility and
intestinal diseases that are connected with colonic motility[12-25].
The studies on how to treat the diseases that are caused by colonic
motility disorder have also been reported[26-35]. But it
still needs a long time for us to recognize the colonic motility
completely.
Recently,
the effects of Chinese herbals on the gastrointestinal motility have
been reported[36-46]. Areca had been used to treat
abdominal distention,constipation, abdominal pain and non-ulcer
dyspepsia,which were considered to be connected with intestinal
motility disorder[47-49]. Whether the clinical use is
connected with its effects on colonic motility The present study
revealed that areca dose dependently stimulated the contractions of
proximal and distal colonic smooth muscle strips of rats. The
exciting actions suggested that areca might caused the colonic
contents to be mixed, stirred, promoted, and even excreted. These
results can partly explained why areca was used to treat intestinal
motility disorder.
Areca
has been showed to stimulate both cholinergic M and N receptors. Our
results showed that the stimulating effects of areca were partly
blocked by atropine but not by hexamethonium. Our results suggested
that the stimulating effects of areca on rat colonic smooth muscle
strips were relevant with M receptor but irrelevant with N receptor.
When M receptor was stimulated,the potential sensitive Ca2+
channel was opened, which will cause the influx of extracellular Ca2+
and then cause the contraction of smooth muscle[50].
Areca might stimulate M receptor and then cause the concentration of
intracellular Ca2+ increased, areca might also act on the
Ca2+ channel receptor directly, which still need to be
further studied. In conclusion, areca stimulates the contractile
activity of colonic smooth muscle of rats in vitro . The
effect of areca is partly relevant with M receptor, but irrelevant
with N receptor.
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