Damage to some contractile and cytoskeleton proteins of the sarcomere in rat neonatal cardiomyocytes after exposure to pavetamine.

Abstract

Pavetamine, a cationic polyamine, is a cardiotoxin that affects ruminants. The animals die of heart failure after a period of four to eight weeks following ingestion of the plants that contain pavetamine. This immunofluorescent study was undertaken in rat neonatal cardiomyocytes (RNCM) to label some of the contractile and cytoskeleton proteins after exposure to pavetamine for 48 h. Myosin and titin were degraded in the RNCM treated with pavetamine and the morphology of alpha-actin was altered, when compared to the untreated cells, while those of beta-tubulin seemed to be unaffected. F-actin was degraded, or even absent, in some of the treated cells. On an ultrastructural level, the sarcomeres were disorganized or disengaged from the Z-lines. Thus, all three contractile proteins of the rat heart were affected by pavetamine treatment, as well as the F-actin of the cytoskeleton. It is possible that these proteins are being degraded by proteases like the calpains and/or cathepsins. The consequence of pavetamine exposure is literally a "broken heart".

• Authors: C E Ellis, D Naicker, K M Basson, C J Botha, R A Meintjes, R A Schultz
• Journal: Toxicon : official journal of the International Society on Toxinology (Toxicon) Vol. 55 Issue 6 Pg. 1071-9 (Jun 01 2010) ISSN: 1879-3150 [Electronic] England
• PMID: 20026156 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
• Copyright: Copyright 2009 Elsevier Ltd. All rights reserved.

Chemical References

• Actins
• Connectin
• Cytoskeletal Proteins
• Muscle Proteins
• Polyamines
• Tubulin
• pavetamine
• Protein Kinases
• Myosins

Topics

• Actins (drug effects, metabolism)
• Animals
• Animals, Newborn
• Cells, Cultured
• Connectin
• Cytoskeletal Proteins (drug effects, metabolism)
• Microscopy, Electron, Transmission
• Muscle Proteins (drug effects, metabolism)
• Myocytes, Cardiac (drug effects, metabolism, ultrastructure)
• Myosins (drug effects, metabolism)
• Polyamines (toxicity)
• Protein Kinases (drug effects, metabolism)
• Rats
• Rats, Sprague-Dawley
• Sarcomeres (drug effects, ultrastructure)
• Tubulin (drug effects, metabolism)