Pacemaker potentials in lymphatic smooth muscle of the guinea-pig mesentery
1. Intracellular microelectrode recordings have been made from lymphatic smooth muscle (SM) to investigate pacemaker mechanisms underlying lymphatic pumping. 2. The SM of small lymphangions or that of short segments, cut from lymphangions of any length, behaved similarly. Both preparations exhibited...
Saved in:
Published in | The Journal of physiology Vol. 471; no. 1; pp. 465 - 479 |
---|---|
Main Author | |
Format | Journal Article |
Language | English |
Published |
Oxford
The Physiological Society
01.11.1993
Blackwell |
Subjects | |
Online Access | Get full text |
Cover
Loading…
Summary: | 1. Intracellular microelectrode recordings have been made from lymphatic smooth muscle (SM) to investigate pacemaker mechanisms
underlying lymphatic pumping. 2. The SM of small lymphangions or that of short segments, cut from lymphangions of any length,
behaved similarly. Both preparations exhibited spontaneous transient depolarizations (STDs) and exhibited simplified electrical
characteristics approximating those of a spherical cell. 3. STDs were found to underlie activation of action potentials and
hence constrictions. 4. The level of STD activity correlated to the pumping activity of lymphangions, the SM from more active
chambers exhibiting increased STD activity. 5. Lymphatic SM exhibited STDs with properties similar to the STDs of mesenteric
veins. STDs appeared to be of myogenic origin as they were present despite denervation or substantial destruction of the endothelium.
6. Noradrenaline enhanced the size and frequency of STDs. 7. STD activity was abolished by chelation of cytosolic Ca2+. 8.
It is proposed that STDs provide a mechanism for pacemaking in the lymphatic SM studied here. Furthermore, it is postulated
that STDs are the consequence of Ca(2+)-dependent pulsatile release of an intracellular messenger, probably Ca2+ itself. This
mechanism provides a novel means for pacemaking. |
---|---|
Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0022-3751 1469-7793 |
DOI: | 10.1113/jphysiol.1993.sp019910 |