Table 2.
Drugs | Effects | Experimental Model | Route and Dosage of Drug Administration |
Local/ Systemic |
Mechanisms of Different Drugs |
References |
---|---|---|---|---|---|---|
Ferrostain-1 | Prevented ROS formation |
Animal model: Folic Acid-induced nephropathy; Cisplatin-induced nephropathy; UUO; Diabetic db/db mice; Pkd1RC/RC and Pkd1flox/flox: Pkhd1-Cre mice |
IP: Pkd1RC/RC and Pkd1flox/flox: Pkhd1-Cre mice: 4 mg/kg/da; Cisplatin-induced nephropathy; 5 mg/kg/day Diabetic db/db mice; 1 mg/kg/day; UUO: 5 mg/kg |
systemic | Inhibition of the upregulation of IL-33; Inhibition HIF-1α/HO-1 pathway; Normalize the iron metabolism and inhibiting cell proliferation through Akt, S6, Stat3 and Rb signal pathways |
[15,43,75,116] |
SRS 16-86 | Ferroptosis inhibition |
Animal model: IRI model |
IP: 2 mg/kg |
systemic | Inhibition of mitochondrial permeability transition, postischemic and toxic renal necrosis. |
[114] |
DFX/DFO | Chelate iron | Animal model: UUO; 5/6 nephrectomy |
DFO: IP: 100 mg/kg/day DFX: Oral: low dose 15 mg/kg/day, moderate dose 30 mg/kg/day high dose 60 mg/kg/day |
systemic | TGF-β1/Smad3, inflammation, and oxidative stress pathways |
[85,92] |
Liproxstain-1 | Ferroptosis inhibition |
Animal model: IRI model |
IP: 10 mg/kg |
systemic | Induces GPX4 expression, reduces COX2 expression and inhibition of the kidney inflammation activation |
[115] |
N-acetyl-l-
cysteine |
Reduce ROS | Animal model: Cisplatin-induced nephropathy |
IP: 50 mg/kg |
systemic | Inhibition of the kidney inflammation activation and the complement system |
[124] |
Rosiglitazone | Decrease ROS | Animal model: STZ-induced diabetic kidneys |
Intragastric: 5 or 20 mg/kg/day Oral: 3 mg/kg/day |
systemic | Inhibition of NF-ĸB activation and MCP-1 expression. |
[125,126] |
CPX-O | Chelate iron | Animal model: Pkd1RC/RC/Pkd2+/− mice |
IP: 10 mg/kg/day |
systemic | Induces ferritin degradation via ferritinophagy |
[118] |
L-buthionine
(S,R)-sulfoximine |
Deprivation of glutamine and cystine |
Animal model: MYC-dependent RCC mouse model |
Oral: 20 mM in drinking water/day |
systemic | GSH synthesis inhibition | [106] |
Artesunate | Induction of ferroptosis |
Cell model: Sunitinib-resistant RCC cells |
20 uM in cultured media |
local | Cell cycle arrest and modulation of cell cycle regulating proteins |
[122] |
CPX-O: Ciclopirox olamine; DFX: Desferriox; DFO: Deferroxamine; ROS: reactive oxygen species; HIF-1α: hypoxia-inducible factor 1-alpha; HO-1: heme oxygenase-1; UUO: unilateral ureteral obstruction; IRI: renal ischemia–reperfusion injury; CKD: chronic kidney disease; GPX4: glutathione peroxidase 4; COX2: cyclooxygenase-2; MCP-1: monocyte chemoattractant protein-1; RCC: renal cell carcinoma; GSH: glutathione.