Adaptation of intestinal muscle in bypassed loops after jejunoileal bypass in rat

1983 ◽  
Vol 244 (6) ◽  
pp. G599-G603
Author(s):  
P. R. Nemeth ◽  
D. J. Kwee ◽  
N. W. Weisbrodt

The function and structure of intestinal smooth muscle in the bypassed intestine of rats with 70% intestinal bypass were compared with the function and structure of muscle from equivalent areas of intestine from transected and nontransected controls. Muscle function was assessed by evaluating changes in intestinal transit. At all times studied after operation, transit in transected controls was identical to that seen in nontransected controls. In the bypassed intestine at 3 days after operation, transit in fasted animals was significantly slower than intestinal transit in either control group. Over a period of 14-35 days, transit in the bypassed intestine of fasted animals returned toward control values. In fed animals, on the other hand, transit was delayed when measured at both 3 and 35 days after bypass operation. These findings demonstrate a persistent change in muscle function in bypassed intestine in response to the ingestion of a meal. No changes in intestinal structure were found when bypassed intestine was compared with tissue from transected controls. Thus there were no indications of mucosal or muscular atrophy in the bypassed intestine. The weights of the combined submucosal, muscular, and serosal layers in the study segments were increased at 35 days after either bypass or transection compared with tissue from nontransected controls. These changes appear to be a nonspecific result of operation.

iScience ◽  
2020 ◽  
Vol 23 (9) ◽  
pp. 101464
Author(s):  
Weilong Zhong ◽  
Bo Sun ◽  
Hao Ruan ◽  
Guang Yang ◽  
Baoxin Qian ◽  
...  

1988 ◽  
Vol 65 (3) ◽  
pp. 1238-1243 ◽  
Author(s):  
G. L. Jones ◽  
C. G. Lane ◽  
E. E. Daniel ◽  
P. M. O'Byrne

Airway epithelium has been reported to release epithelium-derived relaxing factor (EpDRF), which inhibits contraction of airway smooth muscle. This study tested the hypothesis that airway hyperresponsiveness after inhalation of ozone in dogs results from an inability to produce EpDRF. Two groups of five dogs each were studied; one group inhaled ozone, the other dry room air. Ozone-treated dogs developed airway hyperresponsiveness, whereas the control group did not. The acetylcholine provocative concentration decreased from 4.17 (%SE 1.35) to 0.56 mg/ml (%SE 1.24) (P = 0.0006) in the ozone-treated dogs and was 18.76 (%SE 2.04) and 29.77 mg/ml (%SE 2.07) in the air-treated dogs (P = 0.47). In vitro the presence of airway epithelium reduced the constrictor responses to acetylcholine, histamine, serotonin, and KCl in trachealis strips from the control dogs. This effect of epithelium was still present in trachealis strips from dogs with airway hyperresponsiveness. These results demonstrate that EpDRF is released from canine tracheal epithelium, that this function is not impaired in dogs with airway hyperresponsiveness after inhaled ozone, and that loss of EpDRF is not responsible for the development of airway hyperresponsiveness after inhaled ozone in dogs.


Surgery ◽  
1999 ◽  
Vol 125 (3) ◽  
pp. 339-344 ◽  
Author(s):  
Joseph J. Cullen ◽  
David Mercer ◽  
Marilyn Hinkhouse ◽  
Kimberly S. Ephgrave ◽  
Jeffrey L. Conklin

1985 ◽  
Vol 88 (4) ◽  
pp. 958-963 ◽  
Author(s):  
Norman W. Weisbrodt ◽  
Paul R. Nemeth ◽  
Rebecca L. Bowers ◽  
William A. Weems

1993 ◽  
Vol 104 (6) ◽  
pp. 1692-1699 ◽  
Author(s):  
Dianne L. Vermillion ◽  
Jan D. Huizinga ◽  
Robert H. Riddell ◽  
Stephen M. Collins

2013 ◽  
Vol 204 (1) ◽  
pp. 1-5 ◽  
Author(s):  
C. Königer ◽  
F. Worek ◽  
H. Thiermann ◽  
T. Wille

1975 ◽  
Vol 229 (6) ◽  
pp. 1609-1613 ◽  
Author(s):  
A Bortoff ◽  
R Muller

In order to determine whether or not atropine, procaine, and tetrodotoxin (TTX) can stimulate intestinal smooth muscle directly, we examined the effects of these drugs on the mechanical and electrical activities of several types of cat intestinal smooth muscle preparations. The preparations consisted of isolated rings of 1) intact intestinal wall, 2) intact longitudinal and circular muscle, 3) ganglion-free circular muscle, and 4) ganglion-free circular muscle devoid of its dense layer and plexus muscularis profundus. Atropine and procaine (greater than 10(-4) M) stimulated all four types of preparation. On the other hand, TTX (up to 5 X 10(-6) M) stimulated only preparations 1 and 2. It is concluded that whereas atropine and procaine can directly stimulate intestinal smooth muscle, the excitatory effect of TTX is neurally mediated.


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