Excitation of intestinal muscle by atropine, tetrodotoxin, and xylocaine.
نویسنده
چکیده
WOOD, J. D. Excitation of intestinal muscle by atropine, tetrodotoxin, and Xylocaine. Am. J. Physiol. 222(l): li8-125. 1972.-The circular muscle layer of cat jejunum was mechanically and electrically quiescent when equilibrated in Tyrode solution at 37 C. Atropine, procaine, tetrodotoxin, and Xylocaine produced action potentials and a large increase in the amplitude of contractions in the circular muscle. High concentrations of Xylocaine suppressed circular muscle activity. The excitatory response to atropine and Xylocaine did not occur after 7 days of storage at 5 C; suppression by high concentrations of Xylocaine was not affected by storage. Barium chloride produced excitation after 7 days of storage. Circular muscle activity produced by atropine was inhibited by transmural electrical stimulation. This inhibition was not antagonized by guanethidine, but was abolished by procaine, tetrodotoxin, and Xvlocaine. Conducted responses to mechanical stimulation were . more easily elicited and were propagated over greater distances after blockade of enteric neurons. The results indicate that myogenie activity of the circular muscle is continuously inhibited by spontaneously active inhibitory pathways within the enteric nervous system. The mechanism of the excitatory action of the drugs appears to not be directly on the muscle, but to involve removal of inhibition from the muscle by interrupting nervous transmission within the pathways. Myogenic mechanisms trigger action potentials and associated contractions when inhibition is removed.
منابع مشابه
Stimulation of intestinal smooth muscle by atropine, procaine, and tetrodotoxin.
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) ...
متن کاملSecondary excitation of intestinal smooth muscle.
1. A period of stimulation of intrinsic or extrinsic nerves to intestinal muscle is often followed by a secondary contraction. In the present work, the basis for such secondary contractions in the longitudinal muscle of the large bowel of guinea-pigs and rabbits was examined.2. In general, the action of cholinergic nerves did not contribute significantly to the secondary contractions. Concentra...
متن کاملPituitary adenylate cyclase-activating peptide as a neurotransmitter in the canine ileal circular muscle.
Pituitary adenylate cyclase-activating peptide (PACAP)1-27, PACAP1-38, and vasoactive intestinal peptide (VIP) initiated dose-dependent contractions of canine ileal circular muscle after intra-arterial injection in vivo or ex vivo. PACAP1-27- and VIP-induced contractions approached the tissue maximum; VIP was 100-fold less potent. PACAP1-38 was more potent than VIP. PACAP1-27 contractions in vi...
متن کاملElectrical stimulation of esophageal smooth muscle and effects of antagonists.
LUND, GORDON F., AND JAMES CHRISTENSEN. Electrical stimulation of esophageal smooth muscle and effects of antagonists. Am. J. Physiol. 217(5): 1369-1374. 1969.-Smooth muscle strips from the esophageal body of the opossum were arranged to show, separately, responses of longitudinal, circular, and mucosal muscle layers to electrical stimulation by l.O-msec square waves at 30 v. Longitudinal and m...
متن کاملMorphine leads to contraction of the ileal circular muscle via inhibition of the nitrergic pathway in mice.
Morphine inhibits small intestinal transit in mice, although few mu-opioid receptors are present in the ileum. The present study focused on the action of morphine in the isolated mouse ileum to reveal the mechanism by which morphine inhibits mouse small intestinal transit. In the isolated circular muscle, morphine caused tonic contraction. This contraction was potently inhibited by naloxone and...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید
ثبت ناماگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید
ورودعنوان ژورنال:
- The American journal of physiology
دوره 222 1 شماره
صفحات -
تاریخ انتشار 1972