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Macrophage colony-stimulating factor treatment after myocardial infarction attenuates left ventricular dysfunction by accelerating infarct repair.
J Am Coll Cardiol. 2006 Feb 07; 47(3):626-34.JACC

Abstract

OBJECTIVES

We aimed to determine the effects of macrophage colony-stimulating factor (M-CSF) and granulocyte colony-stimulating factor (G-CSF) treatment on both the repair process and ventricular function after myocardial infarction (MI).

BACKGROUND

The M-CSF and G-CSF have multiple potential effects on cells involved in wound repair.

METHODS

Myocardial infarction was induced by 45- or 90-min coronary occlusion and reperfusion in rats with or without subsequent injection of M-CSF (10(6) IU/kg/day) or G-CSF (50 microg/kg/day) for five days. We examined histology and messenger ribonucleic acid (mRNA), and assessed left ventricular function in situ using a conductance catheter.

RESULTS

Five days after MI, M-CSF increased the number of ED-1-positive cells, mRNA levels of transforming growth factor-beta-1, collagen I and III, and collagen fibers within the infarct. Fourteen days after MI, induced by 45-min ischemia, left ventricular end-systolic elastance (Ees) was reduced (1,191 +/- 87 mm Hg/ml vs. 1,812 +/- 150 mm Hg/ml) and both isovolumic relaxation time constant (tau) (11.9 +/- 0.9 ms vs. 8.5 +/- 0.4 ms) and left ventricular end-diastolic volume (LVEDV) (0.225 +/- 0.014 ml vs. 0.172 +/- 0.011 ml) increased versus sham-operated rats. These alterations after MI were attenuated by M-CSF (Ees = 1,650 +/- 146, tau = 9.7 +/- 0.7, LVEDV = 0.199 +/- 0.012) but not by G-CSF. This beneficial effect of M-CSF on Ees was also detected in hearts with MI induced by 90-min ischemia. Furthermore, M-CSF increased collagen content within infarcts and reduced the proportion of thin collagen fibers 14 days after MI. The Ees significantly correlated with infarct collagen content. Nevertheless, neither M-CSF nor G-CSF modified infarct size.

CONCLUSIONS

The M-CSF treatment attenuates deterioration of left ventricular function after MI by accelerating infarct repair.

Authors+Show Affiliations

Second Department of Internal Medicine, Sapporo Medical University School of Medicine, Sapporo, Japan.No affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article
Research Support, Non-U.S. Gov't

Language

eng

PubMed ID

16458148

Citation

Yano, Toshiyuki, et al. "Macrophage Colony-stimulating Factor Treatment After Myocardial Infarction Attenuates Left Ventricular Dysfunction By Accelerating Infarct Repair." Journal of the American College of Cardiology, vol. 47, no. 3, 2006, pp. 626-34.
Yano T, Miura T, Whittaker P, et al. Macrophage colony-stimulating factor treatment after myocardial infarction attenuates left ventricular dysfunction by accelerating infarct repair. J Am Coll Cardiol. 2006;47(3):626-34.
Yano, T., Miura, T., Whittaker, P., Miki, T., Sakamoto, J., Nakamura, Y., Ichikawa, Y., Ikeda, Y., Kobayashi, H., Ohori, K., & Shimamoto, K. (2006). Macrophage colony-stimulating factor treatment after myocardial infarction attenuates left ventricular dysfunction by accelerating infarct repair. Journal of the American College of Cardiology, 47(3), 626-34.
Yano T, et al. Macrophage Colony-stimulating Factor Treatment After Myocardial Infarction Attenuates Left Ventricular Dysfunction By Accelerating Infarct Repair. J Am Coll Cardiol. 2006 Feb 7;47(3):626-34. PubMed PMID: 16458148.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Macrophage colony-stimulating factor treatment after myocardial infarction attenuates left ventricular dysfunction by accelerating infarct repair. AU - Yano,Toshiyuki, AU - Miura,Tetsuji, AU - Whittaker,Peter, AU - Miki,Takayuki, AU - Sakamoto,Jun, AU - Nakamura,Yuichi, AU - Ichikawa,Yoshihiko, AU - Ikeda,Yoshihiro, AU - Kobayashi,Hironori, AU - Ohori,Katsuhiko, AU - Shimamoto,Kazuaki, Y1 - 2006/01/20/ PY - 2005/07/01/received PY - 2005/08/29/revised PY - 2005/09/08/accepted PY - 2006/2/7/pubmed PY - 2006/3/28/medline PY - 2006/2/7/entrez SP - 626 EP - 34 JF - Journal of the American College of Cardiology JO - J Am Coll Cardiol VL - 47 IS - 3 N2 - OBJECTIVES: We aimed to determine the effects of macrophage colony-stimulating factor (M-CSF) and granulocyte colony-stimulating factor (G-CSF) treatment on both the repair process and ventricular function after myocardial infarction (MI). BACKGROUND: The M-CSF and G-CSF have multiple potential effects on cells involved in wound repair. METHODS: Myocardial infarction was induced by 45- or 90-min coronary occlusion and reperfusion in rats with or without subsequent injection of M-CSF (10(6) IU/kg/day) or G-CSF (50 microg/kg/day) for five days. We examined histology and messenger ribonucleic acid (mRNA), and assessed left ventricular function in situ using a conductance catheter. RESULTS: Five days after MI, M-CSF increased the number of ED-1-positive cells, mRNA levels of transforming growth factor-beta-1, collagen I and III, and collagen fibers within the infarct. Fourteen days after MI, induced by 45-min ischemia, left ventricular end-systolic elastance (Ees) was reduced (1,191 +/- 87 mm Hg/ml vs. 1,812 +/- 150 mm Hg/ml) and both isovolumic relaxation time constant (tau) (11.9 +/- 0.9 ms vs. 8.5 +/- 0.4 ms) and left ventricular end-diastolic volume (LVEDV) (0.225 +/- 0.014 ml vs. 0.172 +/- 0.011 ml) increased versus sham-operated rats. These alterations after MI were attenuated by M-CSF (Ees = 1,650 +/- 146, tau = 9.7 +/- 0.7, LVEDV = 0.199 +/- 0.012) but not by G-CSF. This beneficial effect of M-CSF on Ees was also detected in hearts with MI induced by 90-min ischemia. Furthermore, M-CSF increased collagen content within infarcts and reduced the proportion of thin collagen fibers 14 days after MI. The Ees significantly correlated with infarct collagen content. Nevertheless, neither M-CSF nor G-CSF modified infarct size. CONCLUSIONS: The M-CSF treatment attenuates deterioration of left ventricular function after MI by accelerating infarct repair. SN - 1558-3597 UR - https://www.unboundmedicine.com/medline/citation/16458148/Macrophage_colony_stimulating_factor_treatment_after_myocardial_infarction_attenuates_left_ventricular_dysfunction_by_accelerating_infarct_repair_ L2 - https://linkinghub.elsevier.com/retrieve/pii/S0735-1097(05)02628-8 DB - PRIME DP - Unbound Medicine ER -