Calcium and the contractile response to prostaglandin in the smooth muscle of guinea-pig stomach

Summary In the longitudinal smooth muscle of guinea-pig stomach, verapamil (10^–5 M) which showed marked suppression of high K-induced contractures, did not suppress the contractile response to PGE₁ (1.5×10^–9 to 10^–6 M) markedly. These results suggest that the contractile mechanism of PGE₁ in guinea-pig stomach may mainly depend on a release of bound Ca in the cell and partly depend on a Ca influx from the extracellular origin.     

Comparison of rat,mouse, guinea-pig and human slow reacting substance of anaphylaxis (SRS-A)

Summary Slow reacting substance of anaphylaxis obtained from rat, mouse, guinea-pig and human tissues have exhibited similar biological activity and have reacted in the same way to chemical and enzymatic treatments. It is concluded that they appear to be the same substance or a similar class of compounds.Acknowledgments. The authors are grateful to Le Conseil de Recherche en Santé du Québec and to Fisons Ltd for financial support. This work was also partly supported by a grant to the late Dr R. P. Orange from the Medical Research Council of Canada (MT-4605).     

Pathways for excitatory and inhibitory innervation to the guinea-pig tracheal smooth muscle

Summary The trachea receives excitatory cholinergic innervation from the vagus nerve and the stellate ganglion. Inhibitory adrenergic fibres have the same sources. Those in the vagus nerve probably derive from high vagosympathetic anastomoses. Nonadrenergic inhibitory fibres have a preganglionic vagal supply.This study has been supported by grants from Magnus Bergvall Memorial Found and Harald and Greta Jeansson Foundation.     

Comparison of rat, mouse, guinea-pig and human slow reacting substance of anaphylaxis (SRS-A).

Slow reacting substance of anaphylaxis obtained from rat, mouse, guinea-pig and human tissues have exhibited similar biological activity and have reacted in the same way to chemical and enzymatic treatments. It is concluded that they appear to be the same substance or a similar class of compounds.     

Size ofTrichinella spiralis (nematoda) muscle cysts in the rat,mouse and guinea-pig

Zusammenfassung Bei Ratte, Maus und Meerschweinchen ist die Grösse der Muskelzysten vonTrichinella spiralis 60 Tage nach standardisierter experimenteller Infektion bestimmt worden. Die Grösse der Muskelzysten variierte bei jeder der 3 untersuchten Tierarten erheblich. Bei der Ratte wurden durchschnittlich grössere Muskelzysten vonT. spiralis gefunden als bei der Maus, bei der die Muskelzysten wiederum durchschschnittlich grösser waren als beim Meerschweinchen. Die Zystengrösse vonT. spiralis scheint demnach vom Stoffwechsel der jeweils als Wirt dienenden Tierart abhängig zu sein.     

Pathways for excitatory and inhibitory innervation to the guinea-pig tracheal smooth muscle.

The trachea receives excitatory cholinergic innervation from the vagus nerve and the stellate ganglion. Inhibitory adrenergic fibres have the same sources. Those in the vagus nerve probably derive from high vagosympathetic anastomoses. Nonadrenergic inhibitory fibres have a preganglionic vagal supply.     

Spikes of smooth muscle in calcium-free solution (isolated taenia coli of the guinea-pig)

Zusammenfassung An der glatten Darmmuskulatur (Taenia coli) des Meerschweinchens konnten nach völligem Entzug von Kalzium (und Magnesium) aus der Nährlösung über lange Zeit Spikes gemessen werden. Diese kalziumfreien Spikes werden, im Gegensatz zu den Spikes unter normalen Bedingungen, durch Tetrodotoxin 10^–5 blockiert, und sie werden wie die normalen Spikes mit 100fach niedrigerer Schwelle durch Manganionen blockiert. Es wird angenommen, daß Na-Ionen die für diese Spikes verantwortlichen Ladungsträger sind.

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This work was supported by a grant from the Deutsche Forschungsgemeinschaft (No. Go 130/7).     

The effect of urethane on histamine-induced contraction of guinea-pig tracheal smooth muscle

Summary Urethane possesses a direct depressant action on histamine-induced contractions of guinea-pig tracheal smooth muscle both in vivo and in vitro.     

Cholinergic mechanisms in the production of focal cortical slow waves

Summary Microiontophoretic application of scopolamine and atropine usually induced or increased focal cortical slow waves of under 3 Hz and abolished or decreased focal fast waves of over 6 Hz whereas acetylcholine iontophoresis and electrical stimulation of the mesencephalic reticular formation had the opposite effect, suggesting that focal cortical slow waves may be due to the interruption of cholinergic input from the reticular formation.This study was supported by funds from the Veterans Administration and by NIH research grant NS 06820.We thank Mr C.C. Smathers, Jr, for his technical help.     

Contractile properties of fast muscle preparations regenerating in slow muscle beds

Summary Mechanical evidence is presented to show that fast muscle tissue regenerating in the bed of a slow muscle, and innervated by the slow muscle nerve, has contractile properties identical to those of a slow muscle regenerating in its own bed. The results do not support the idea that regenerating fast muscles are partially resistant to the transforming effects of a slow nerve.This investigation was supported in part by NIH grants 1-RO1-NS-14033 and 1-T32-07224.     

Energy metabolism and transduction in smooth muscle

Early investigations into the nature of the coupling between energy transduction and metabolism in smooth muscle, particularly from the laboratories of Bülbring and Lundholm, suggested that specific metabolic pathways could independently supply energy for ion transport and actin-myosin interactions. Subsequent work has solidified the concept that oxidative phosphorylation is specifically coupled to tension generation and maintenance, whereas, aerobic glycolysis is not only a vital characteristic of smooth muscle metabolism, but also is likely to be independently coupled to Na-K transport at the plasmalemma. The independence of oxidative and glycolytic metabolism is reflected as a compartmentation of carbohydrate metabolism in the porcine carotid artery. The coupling of these independent metabolic pathways with specific energy utilizing processes, indicates a means by which energy production and transduction can be closely and efficiently regulated. The coupling of glycogenolysis to mitochondrial respiration may have evolved as a direct response to the energetic needs of VSM. That is, the large glycogenolytic response in the initial minutes of stimulation may be necessary to maximize the cellular production of ATP during the presteady state. Likewise, the coupling between aerobic glycolysis and Na-K transport indicates a sensitive and efficient means of coordinating energy metabolism with ion transport at the membrane level. Additionally, the regulation of substrate supply, i.e. glucose transport, also may be closely coordinated with changes in ion transport. One may speculate that alterations in the microenvironment of each compartment can independently regulate intermediary metabolism and therefore allow the cell to quickly and efficiently respond to localized stimuli. Thus, stimulation of Na-K transport could effectively regulate energy production at the membrane level without mobilizing or competing with the energy transduction of other cellular processes. This compartmentation of energy utilization may be highly advantageous, since oxidative metabolism is closely coordinated with mechanical activity and therefore regulation of blood flow. Future investigations will attempt to elucidate which intracellular signals which are responsible for the regulation of these functionally independent compartments of energy metabolism and transduction in VSM. In more general terms, our findings provide a basis from which future questions concerning the regulation of cellular metabolism must be directed. The cellular cytoplasm can no longer be envisioned as a homogeneous compartment, but rather a complex array of functional subcompartments which may be individual     

Histochemical fibre types in striated muscle from the guinea-pig oesophagus

Summary Histochemical techniques have been used to classify the striated muscle fibres found in the guinea-pig oesophagus. The functional significance of these results is discussed.     

TRAIL promotes the survival,migration and proliferation of vascular smooth muscle cells

Human and rat primary sub-cultured vascular smooth muscle cells (VSMCs) showed clear expression of the death receptors TRAIL-R1 and TRAIL-R2; however, recombinant soluble TRAIL did not induce cell death when added to these cells. TRAIL tended to protect rat VSMCs from apoptosis induced either by inflammatory cytokines tumor necrosis factor- + interleukin-1 + interferon- or by prolonged serum withdrawal, and promoted a significant increase in VSMC proliferation and migration. Of note, all the biological effects induced by TRAIL were significantly inhibited by pharmacological inhibitors of the ERK pathway. Western blot analysis consistently showed that TRAIL induced a significant activation of ERK1/2, and a much weaker phosphorylation of Akt, while it did not affect the p38/MAPK pathway. Taken together, these data strengthen the notion that the TRAIL/TRAIL-R system likely plays a role in the biology of the vascular system by affecting the survival, migration and proliferation of VSMCs.Received 6 May 2004; received after revision 7 June 2004; accepted 8 June 2004     

Nervous control of smooth muscle by transmitters,cotransmitters and modulators

Conclusion The part played by peripheral neuroeffector control mechanisms has been underestimated. These are additional to central and ganglionic control mechanisms and are much more elaborate than originally thought. While the classical view is that the autonomic nervous system consists largely of antagonistic cholinergic and adrenergic nerves, about sixteen putative neurotransmitters have been proposed in autonomic nerves in the past few years, including various monoamines, polypeptides, purines and amino acids. Modulatory transmitter mechanisms have also been recognized, including prejunctional inhibition or enhancement of transmitter release, postjunctional modulation of transmitter action, and the secondary involvement of locally synthesized hormones and prostaglandins. The existence of more than one transmitter substance in some nerves is now widely recognized, and suggestions have been made about the ways that this can lead to differential peripheral control mechanisms at nerve terminals themselves. The cotransmitters always have synergistic actions on postjunctional effector cells, but two different operating mechanisms are postulated. 1) If both substances are stored in the same vesicles (for example, ACh or NA with ATP), release is closely parallel at all impulse frequencies. Upon release, the cotransmitter, in addition to having a direct action on postjunctional cells, may facilitate the action of the other transmitter and/or act as an inhibitor of its release. Differential actions at different impulse frequencies are achieved post-junctionally by ATP and NA acting via EJP-spike and spike-independent mechanisms, respectively. 2) If the two substances are stored in separate vesicle types (for example ACh or NA with some peptides), then differential release is possible at different impulse frequencies; the peptides released at higher frequencies modulate the role of the classical transmitter, by both prejunctional enhancement of its release and post-junctional facilitation of its action.