Abstract:1 Peripheral nerve pathways responsible for adrenergic inhibition of mechanical and electrical activities in the chicken rectum and receptors mediating the adrenergic inhibition were investigated in isolated extrinsically-innervated rectum of the chicken. 2 Electrical stimulation ofthe anal end (Ra) or the ileal cut end (Ri) of Remak's nerve, or perivascular nerves (P) elicited relaxation of the rectum pretreated with atropine (0.5 JM) and hexamethonium (0.3 mM) to block the cholinergic and non-cholinergic, no… Show more
“…The resting membrane potential ranged between -42 and -68 mV, giving a mean of -55-0±0-6 mV (n = 95). This value was somewhat larger than that of the longitudinal muscle of the chicken rectum (Komori & Ohashi, 1987). Some preparations (70%) were spontaneously active and exhibited spontaneous membrane depolarizations in the early period of each experiment, during which the resting membrane potential was -55 mV or more.…”
Section: Electrical Activitiesmentioning
confidence: 74%
“…The membrane depolarizations (referred to as slow action potentials in the Results), which are spontaneous or electrically evoked, in the circular muscle of chicken rectum are similar in temporal parameters and amplitude to the slow waves in other gastrointestinal smooth muscles of many species (see . The slow depolarization is unlikely to be electrotonic spread from the longitudinal muscle, because such slow changes in membrane potential have not been observed in the longitudinal muscle of chicken rectum (Komori et al 1980;Komori & Ohashi, 1987). The effectiveness of D600 in suppressing discharge of the slow depolarization can be interpreted as an indication for involvement of a Ca21 inward current in the generation.…”
Section: Discussionmentioning
confidence: 97%
“…Nonadrenergic, non-cholinergic neurones whose cell bodies are located in Remak's ganglia (Kanazawa, Ohashi & Takewaki, 1980) are mainly responsible for the excitatory innervation, and excitatory junction potentials are recorded intracellularly from the smooth muscle cells Komori & Ohashi, 1982). Adrenergic nerve fibres innervating the muscle have been also demonstrated in the electrophysiological studies, and electrical stimulation of these fibres at a relatively high frequency produces membrane hyperpolarization, inhibits discharges of the action potentials and in turn causes relaxation (Komori & Ohashi, 1987). Although the circular muscle of chicken rectum has been suggested to play an essential role in storing and expelling the contents, little is known about the electrical membrane properties or about its innervation.…”
SUMMARY1. Membrane properties and innervation of the circular muscle of chicken rectum were investigated by recording intracellularly electrotonic potentials evoked by passing current, and excitatory and inhibitory junction potentials (EJPs and IJPs) evoked by electrical stimulation of the extrinsic or intrinsic nerves.2. The membrane potential was -55 + 06 mV (n = 95). Action potentials of long duration (P12-4-0 s) discharged spontaneously, or were generated when the membrane depolarization due to either electrotonic potential or EJP reached the threshold. The drug D600 blocked the generation of action potentials.3. Electrotonic potentials spread fairly well in the longitudinal direction of the muscle fibres but not in the transverse direction. The longitudinal space constant was 1-7+0-2 mm (n = 10) and the membrane time constant was 205+ 21 ms (n = 10).4. Field stimulation of intramural nerves evoked an EJP followed by a longlasting IJP (3-12 s in total duration) in most cells, and an EJP alone or an IJP alone in a small number of cells. The EJP and IJP were preserved in the simultaneous presence of atropine and guanethidine, but abolished with tetrodotoxin.5. Stimulation of Remak's nerve trunk or its branches produced EJPs which were atropine resistant and guanethidine resistant just like the EJP elicited by intramural nerve stimulation. The extrinsic nerve stimulation was ineffective in eliciting IJPs.6. The EJP amplitude declined in a linear manner as the distance from the stimulating site of intramural nerves was increased. The decline was much greater along the transverse axis than the longitudinal axis of circular muscle fibres.7. The reversal potential for the EJP was estimated by extrapolation to be about -15-3+003 mV (n = 7).8. Apamin did not inhibit the IJP. During the hyperpolarization of a single IJP or summed IJPs, electrotonic potentials remained unchanged or slightly decreased in amplitude.
“…The resting membrane potential ranged between -42 and -68 mV, giving a mean of -55-0±0-6 mV (n = 95). This value was somewhat larger than that of the longitudinal muscle of the chicken rectum (Komori & Ohashi, 1987). Some preparations (70%) were spontaneously active and exhibited spontaneous membrane depolarizations in the early period of each experiment, during which the resting membrane potential was -55 mV or more.…”
Section: Electrical Activitiesmentioning
confidence: 74%
“…The membrane depolarizations (referred to as slow action potentials in the Results), which are spontaneous or electrically evoked, in the circular muscle of chicken rectum are similar in temporal parameters and amplitude to the slow waves in other gastrointestinal smooth muscles of many species (see . The slow depolarization is unlikely to be electrotonic spread from the longitudinal muscle, because such slow changes in membrane potential have not been observed in the longitudinal muscle of chicken rectum (Komori et al 1980;Komori & Ohashi, 1987). The effectiveness of D600 in suppressing discharge of the slow depolarization can be interpreted as an indication for involvement of a Ca21 inward current in the generation.…”
Section: Discussionmentioning
confidence: 97%
“…Nonadrenergic, non-cholinergic neurones whose cell bodies are located in Remak's ganglia (Kanazawa, Ohashi & Takewaki, 1980) are mainly responsible for the excitatory innervation, and excitatory junction potentials are recorded intracellularly from the smooth muscle cells Komori & Ohashi, 1982). Adrenergic nerve fibres innervating the muscle have been also demonstrated in the electrophysiological studies, and electrical stimulation of these fibres at a relatively high frequency produces membrane hyperpolarization, inhibits discharges of the action potentials and in turn causes relaxation (Komori & Ohashi, 1987). Although the circular muscle of chicken rectum has been suggested to play an essential role in storing and expelling the contents, little is known about the electrical membrane properties or about its innervation.…”
SUMMARY1. Membrane properties and innervation of the circular muscle of chicken rectum were investigated by recording intracellularly electrotonic potentials evoked by passing current, and excitatory and inhibitory junction potentials (EJPs and IJPs) evoked by electrical stimulation of the extrinsic or intrinsic nerves.2. The membrane potential was -55 + 06 mV (n = 95). Action potentials of long duration (P12-4-0 s) discharged spontaneously, or were generated when the membrane depolarization due to either electrotonic potential or EJP reached the threshold. The drug D600 blocked the generation of action potentials.3. Electrotonic potentials spread fairly well in the longitudinal direction of the muscle fibres but not in the transverse direction. The longitudinal space constant was 1-7+0-2 mm (n = 10) and the membrane time constant was 205+ 21 ms (n = 10).4. Field stimulation of intramural nerves evoked an EJP followed by a longlasting IJP (3-12 s in total duration) in most cells, and an EJP alone or an IJP alone in a small number of cells. The EJP and IJP were preserved in the simultaneous presence of atropine and guanethidine, but abolished with tetrodotoxin.5. Stimulation of Remak's nerve trunk or its branches produced EJPs which were atropine resistant and guanethidine resistant just like the EJP elicited by intramural nerve stimulation. The extrinsic nerve stimulation was ineffective in eliciting IJPs.6. The EJP amplitude declined in a linear manner as the distance from the stimulating site of intramural nerves was increased. The decline was much greater along the transverse axis than the longitudinal axis of circular muscle fibres.7. The reversal potential for the EJP was estimated by extrapolation to be about -15-3+003 mV (n = 7).8. Apamin did not inhibit the IJP. During the hyperpolarization of a single IJP or summed IJPs, electrotonic potentials remained unchanged or slightly decreased in amplitude.
“…Ten birds were killed by an overdose of halothane anaesthetic. The rectum, jejunum and attached mesentery with Remak's nerve and blood vessels were quickly excised and immersed into cold modified Krebs'-Henseleit solution: 118.9 mM NaCl, 4.6 mM KCl, 1.8 mM CaCl 2 , 2.4 mM MgSO 4, 1.2 mM KH 2 PO 4 , 25.0 mM NaHCO 3 and 11.1 mM glucose bubbled with 5% CO 2 and 95% O 2 (Komori and Ohashi 1987) maintained at 4°C. The gut contents were flushed from the lumen and the tissue washed in several changes of fresh Krebs' solution.…”
Section: Tissuementioning
confidence: 99%
“…Electrophysiological and pharmacological studies have demonstrated that Remak's nerve participates in the regulation of gut motility (Bartlet and Hassan 1971;Hodgkiss 1984a,b;Komori et al 1986Komori et al , 1988Komori and Ohashi 1987). The nature of this control is unknown.…”
Micro-injections of biocytin were made into neurons in whole-mount preparations of Remak's nerve of the domestic fowl to visualise the morphology and projections of Remak's neurons. Remak's neurons were classified into four distinct morphological types. Remak type-I and -II neurons had a morphology resembling that of mammalian sympathetic neurons. Type-I neurons (found only in juxta-jejunal ganglia) had numerous primary dendritic processes (8-14) with large dendritic fields and extensive dendritic arborizations. Type-II neurons had 2-9 primary dendritic processes, large dendritic fields and sparse dendritic branching. These were found in similar numbers in juxta-rectal and juxta-jejunal ganglia. Remak type-III neurons were the most numerous cell type of juxta-rectal ganglia. They had small cell somata and short dendritic processes that branched infrequently. Remak type-IV neurons (found only in juxta-jejunal ganglia) had a morphology resembling that of invertebrate neurons in that they possessed a prominent long tapering axon from which most of the numerous long dendritic processes emerged. In juxta-jejunal ganglia, all type-IV and most type-I, -II and -III neurons projected orally, whereas axons of juxta-rectal neurons (types II and III) projected either orally or aborally, or projected directly into a lateral nerve bundle supplying the gut. These regional differences in neuron types and axonal projections suggest that different neural circuits exist between Remak's nerve and the small and large intestine.
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