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Merck
  • Leptin suppresses non-apoptotic cell death in ischemic rat cardiomyocytes by reduction of iPLA(2) activity.

Leptin suppresses non-apoptotic cell death in ischemic rat cardiomyocytes by reduction of iPLA(2) activity.

Biochemical and biophysical research communications (2015-05-17)
Tomoka Takatani-Nakase, Koichi Takahashi
要旨

Caspase-independent, non-apoptotic cell death is an important therapeutic target in myocardial ischemia. Leptin, an adipose-derived hormone, is known to exhibit cytoprotective effects on the ischemic heart, but the mechanisms are poorly understood. In this research, we found that pretreatment of leptin strongly suppressed ischemic-augmented nuclear shrinkage and non-apoptotic cell death on cardiomyocytes. Leptin was also shown to significantly inhibit the activity of iPLA2, which is considered to play crucial roles in non-apoptotic cell death, resulting in effective prevention of ischemia-induced myocyte death. These findings provide the first evidence of a protective mechanism of leptin against ischemia-induced non-apoptotic cardiomyocyte death.

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Sigma-Aldrich
ヨウ化プロピジウム, ≥94.0% (HPLC)
Sigma-Aldrich
ピルビン酸, 98%
Sigma-Aldrich
セレン, powder, −100 mesh, 99.99% trace metals basis
Sigma-Aldrich
セレン, powder, −100 mesh, ≥99.5% trace metals basis
Sigma-Aldrich
ピルビン酸, ≥97%, FG
Sigma-Aldrich
ピルビン酸, 95%
Sigma-Aldrich
セレン, pellets, <5 mm particle size, ≥99.999% trace metals basis
Sigma-Aldrich
セレン, pellets, <5 mm, ≥99.99% trace metals basis
Sigma-Aldrich
ピルビン酸, natural, ≥95%, FG
Sigma-Aldrich
ヨウ化プロピジウム 溶液
セレン, foil, 25x25mm, thickness 3mm, 99.95%
セレン, pellets, < 5mm, ≥99.999%