PulseExploreJournal ClubDebatesTrendingResearchersJournals
Instagram
HomeExploreJournal ClubTrending
Synapse
⌘+K
Synapse
July 30, 2009Circulation Heart Failure162 citations

Characterization of an Extensive Transverse Tubular Network in Sheep Atrial Myocytes and its Depletion in Heart Failure

View Full Paper
KDKatharine M. DibbJCJessica D. ClarkeMHM Horn

Key Result

In sheep atrial myocytes, heart failure induced by rapid ventricular pacing resulted in an almost complete loss of t-tubules, increasing the distance of 50% of voxels from a membrane from 0.88 to 2.04 micrometers.

Key Points

  • This research aims to characterize the t-tubule network in sheep atrial myocytes and its role in calcium dynamics, particularly in heart failure.
  • Sheep left atrial myocytes were stained with di-4-ANEPPS to visualize the t-tubule network.
  • The distance of voxels from a membrane was measured in control and heart failure conditions.
  • Control myocytes had an extensive t-tubule network with voxels 0.88 ± 0.04 microm from a membrane.
  • In heart failure, the network was nearly completely lost, with voxels 2.04 ± 0.08 microm from a membrane.
  • Early Ca(2+) release was significantly disrupted in heart failure, indicating altered calcium dynamics.

Structured PICO

P
Population
Sheep left atrial myocytes from control and rapid ventricular pacing-induced heart failure models.
E
Exposure
Heart failure induced by rapid ventricular pacing
C
Comparator
Control sheep atrial myocytes
O
Outcome
Presence and structure of t-tubule network and intracellular Ca(2+) release profilesurrogate

Sheep atrial myocytes possess a substantial t-tubule network that synchronizes systolic Ca(2+) transients, which is markedly disrupted in heart failure.

Main Result

Absolute Event Rate: 2.04% vs 0.88%

Abstract

BACKGROUND: In ventricular myocytes, the majority of structures that couple excitation to the systolic rise of Ca(2+) are located at the transverse tubular (t-tubule) membrane. In the failing ventricle, disorganization of t-tubules disrupts excitation contraction coupling. The t-tubule membrane is virtually absent in the atria of small mammals resulting in spatiotemporally distinct profiles of intracellular Ca(2+) release on stimulation in atrial and ventricular cells. The aims of this study were to determine (i) whether atrial myocytes from a large mammal (sheep) possess t-tubules, (ii) whether these are functionally important, and (iii) whether they are disrupted in heart failure. METHODS AND RESULTS: Sheep left atrial myocytes were stained with di-4-ANEPPS. Nearly all control cells had an extensive t-tubule network resulting in each voxel in the cell being nearer to a membrane (sarcolemma or t-tubule) than would otherwise be the case. T-tubules decrease the distance of 50% of voxels from a membrane from 3.35 + or - 0.15 to 0.88 + or- 0.04 microm. During depolarization, intracellular Ca(2+) rises simultaneously at the cell periphery and center. In heart failure induced by rapid ventricular pacing, there was an almost complete loss of atrial t-tubules. The distance of 50% of voxels from a membrane increased to 2.04 + or - 0.08 microm, and there was a loss of early Ca(2+) release from the cell center. CONCLUSIONS: Sheep atrial myocytes possess a substantial t-tubule network that synchronizes the systolic Ca(2+) transient. In heart failure, this network is markedly disrupted. This may play an important role in changes of atrial function in heart failure.

Ask AI
Helpful
Bookmark
Share
View Full Paper

Cite This Study

Dibb et al. (2009) studied Heart failure. Heart failure induced by rapid ventricular pacing vs. Control cells was evaluated on Distance of 50% of voxels from a membrane (micrometers). In sheep atrial myocytes, heart failure induced by rapid ventricular pacing resulted in an almost complete loss of t-tubules, increasing the distance of 50% of voxels from a membrane from 0.88 to 2.04 micrometers.

synapsesocial.com/papers/6a22665cb04f494b2753d1bfhttps://doi.org/10.1161/circheartfailure.109.852228
Ask AI
Helpful
Bookmark
Share
View Full Paper