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Updated: Aug 19, 2026

A Doxorubicin-induced Cardiomyopathy Model in Adult Zebrafish
Published on: June 7, 2018
Effect of octreotide in the prevention of doxorubicin cardiotoxicity
Cem Barçin1, Hürkan Kurşaklioğlu, Mükerrem Safali
1Department of Cardiology, Gulhane Military Medical Academy, Ankara, Turkey. cembarcin@yahoo.com
Objective:
A precise method for prevention from doxorubicin cardiotoxicity is not known. We examined whether octreotide has a protective effect against doxorubicin cardiotoxicity.
Methods:
New Zealand rabbits (n=44) were divided into 4 groups according to drugs given: Group A (n=12) doxorubicin and octreotide, Group B (n=12) only doxorubicin, Group C (n=10) only octreotide and Group D (n=10) only saline. Effects of the drugs were evaluated in terms of histopathological score, fractional shortening (FS) and prolongation of the QTc interval.
Results:
Mean pathological score for cardiotoxicity (Group A: 3.7+/-0.5, Group B: 3.9+/-0.3), prolongation of QTc (Group A: from 244.5+/-21.2 ms to 282.9+/-25.9 ms, p<0.0001; Group B: from 248.5+/-17.7 ms to 298.3+/-13.7 ms, p<0.00001) and the rate of decrease in FS (Group A: from 34.4+/-2.0 to 28.0+/-2.0, p<0.05; Group B: from 35.1+/-1.9 to 24.8+/-1.3, p<0.05) were higher in Group B when compared to Group A, but only difference in the rate of decrease in FS was statistically significant (p<0.001). None of these variables changed significantly in groups C and D.
Conclusion:
In this preliminary study, octreotide seems not to reduce doxorubicin cardiotoxicity. On the other hand, a consistent tendency of decreased cardiotoxicity in octreotide+doxorubicin group was observed, although only the difference in FS decrease was significant. Further investigations are needed to address the issue of the extent and the mechanisms of this effect.
Insights
Octreotide did not significantly prevent doxorubicin cardiotoxicity in rabbits. However, a trend towards reduced cardiac damage was observed, warranting further investigation into its potential protective mechanisms.
Area of Science:
- Cardiology
- Pharmacology
- Oncology
Background:
- Doxorubicin is a widely used chemotherapy agent with known cardiotoxic side effects.
- Effective strategies for preventing doxorubicin-induced cardiotoxicity remain an unmet clinical need.
- Octreotide, a somatostatin analog, has been explored for various therapeutic applications.
Purpose of the Study:
- To investigate the potential protective effect of octreotide against doxorubicin-induced cardiotoxicity.
- To evaluate the impact of octreotide co-administration on cardiac function and structure in a rabbit model.
Main Methods:
- New Zealand rabbits were divided into four groups: doxorubicin + octreotide, doxorubicin alone, octreotide alone, and saline control.
- Cardiac function was assessed by measuring fractional shortening (FS) and QTc interval.
- Histopathological scoring was used to evaluate the extent of cardiotoxicity.
Main Results:
- Doxorubicin administration led to significant QTc interval prolongation and a decrease in fractional shortening.
- While octreotide co-administration showed a trend towards reduced cardiotoxicity, only the difference in the rate of decrease in FS was statistically significant compared to doxorubicin alone.
- No significant changes in cardiac parameters were observed in the octreotide-only or saline groups.
Conclusions:
- Octreotide did not demonstrate a significant protective effect against doxorubicin cardiotoxicity in this preliminary study.
- A consistent tendency towards decreased cardiotoxicity was observed in the group receiving both octreotide and doxorubicin.
- Further research is required to elucidate the extent and mechanisms of octreotide's potential effect on doxorubicin-induced cardiac damage.
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