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. 2021 Oct 19;10(10):1643. doi: 10.3390/antiox10101643

Table 3.

Cardioprotective, neuroprotective and renoprotective effects of apigenin following different toxic stimuli and during dysmetabolic-induced organ dysfunction.

Organ Effects of Apigenin through Antioxidant Action Effects of Apigenin during Dysmetabolic-Dependent Organ Alteration
  • -

    Protection against ISO-induced myocardial hypertrophy and myocardial infarction in vitro and in vivo models [86,87,88,89]

  • -

    Protection against high glucose-dependent endothelial dysfunction in vitro [100]

  • -

    Improvement of hypertension, cardiac hypertrophy and fibrosis in vivo [90]

  • -

    Amelioration of lipid profile and LDL oxidation in hyperlipidaemic rats [101]

  • -

    Protection against diabetes-mellitus-induced cardiac alteration in vivo [102,103]

HEART
  • -

    Protection against DOX-dependent cardiotoxicity [91,93,94,95]

  • -

    Protection against hypertensive cardiac hypertrophy and abnormal myocardial glucolipid metabolism in vivo [105,106]

  • -

    Improvement of vascular endothelial and cardiac function in vivo during aging or following I/R insult [96,97]

  • -

    Improvement of cardiac functions, cardiac hypertrophy and interstitial fibrosis in a mouse model of diabetic cardiomyopathy [107]

  • -

    Protection against I/R-induced damage in H9c2 cells [98]

  • -

    Improvement of glucose intolerance in miRNA103-overexpressing transgenic mice and glucose/lipid homeostasis [108,109,110,111]

  • -

    Neuroprotection against kainic-acid-induced ferroptosis and oxidative stress in vivo [113]

BRAIN
  • -

    Improvement of brain damage and neurological deficiencies following ischemic stroke, I/R damage or subarachnoid haemorrhage [116,118,119]

  • -

    Protective hippocampal action in rats fed high fat, fructose diet [120]

KIDNEY
  • -

    Protection against cisplatin-induced nephrotoxicity or DOX-induced nephrotoxicity in vivo [123,124,125]

  • -

    Beneficial preconditioning effect

against renal I/R injury [126]
  • -

    Protection against renal pathological changes in mesoporous silica-nanoparticles-treated mice [127]

  • -

    Reduction of NiONPs-induced kidney damage and carbon-nanotubes-induced mitochondrial dysfunction in rat models [29]

  • -

    Protection against diabetic nephropathy in a rat model [132]

  • -

    Improvement of tubulointerstitial fibrosis and tubular cell damage in Zucker diabetic fatty (fa/fa) rats [135]

ISO = isoproterenol, DOX = doxorubicin, LDL = low density lipoproteins, I/R = ischaemia/reperfusion, NiONPs = nickel oxide nanoparticles.