In (1904) Magnus described the technique of using excised segments of intest ines bathed by physiological sa l t solut ions. I n i t i a l l y , the smooth muscle ac t i v i t y was recorded by mechanical methods. Today, in addit ion to the mechanical recording under isotonic, isometric, and auxotonic condit ions, e lect r ica l ac t i v i t y is studied by i n t race l l u la r and ex t race l lu la r electrodes. Even though each method has l imi ta t ions, the information obtained has resu l t ed in advancement of smooth muscle physiology. However, the ex is t ing mechanical recording procedures have the fol lowing l imi ta t ions (I) each smooth muscle preparation must serve as i t own control , thus precluding "in vivo" exposures, (2) each evaluation of an e l i c i t ed response is based pr imari ly on visual impressions of the trace recordings, rather than automative quant i tat ive analysis and (3) the primary parameter has been the contraction, e i ther i t s presence, absence or magnitude. Studies on smooth muscle e lec t r ica l ac t i v i t y and i t s relat ionship to contract ions have suggested ( i ) that smooth muscle's e lect r ica l ac t i v i t y is composed of slow-waves and superimposed action potent ials whose combined action is required to i n i t i a t e a contraction, (2) that the slow waves(sometimes referred to as ei ther basic elect r i c rhythms or pacesetter potent ia ls) or ig inate in the long i tud i nal muscle's pacemaker cel ls and regulate the frequency of contractions, (3) that the superimposed action potent ials determine the magnitude of contraction, (4) that both longitudinal and c i rcu lar muscle layers are required for propagation of the elect r i c a l ac t i v i t y . In addit ion, Connor, et al (1976) have suggested that the slow waves are associated with cel l metabolism by means of electrogenic ion t ransport . Thus, i t appeared that "in v i t ro" measurements of the intact gut segment's frequency of contraction should be a suitable ind i rect method for monitoring smooth muscle ac t i v i t y , in par t icu lar , the slow-wave ac t i v i t y of i t s pacemaker ce l ls . This approach was fac i l i t a ted by using a microprocessor based system designed and constructed in th is laboratory. Since the frequency of contraction is the reciprocal of the intercont ract ion in terva l , the l a t t e r was measured by the microprocessor based system. The automative quant i tat ive measurements of 512 consecutive spontaneous contractions provided an i ntercont racti on interval histogram for each gut segment s imi lar to the interspike interval for neuronal spike t ra ins (MacGregory & Lewis, 1971).
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