Table 4: Pre-clinical and clinical studies with curcumin.
Mechanisms of action/clinical action |
Evaluation |
References |
Anti-inflammatory action: Decreased M1G levels from 4.8 F 2.9 adducts per 107 nucleotides to 2.0 F 1.8 adducts per 107 nucleotides |
Human Patients colorectal cancer |
GARCEA, et al. [41] |
Phase I dose escalation: Toxicity at 8,000 mg/d |
Human Patients Breast cancer |
BAYET-ROBERT, et al. [42] |
Association with PLGA Nanoparticles: Improve bioavailability, increased solubility, higher release rate in intestinal juice, enhanced absorption by improved permeability, inhibition of P-glycoprotein (P-gp)-mediated efflux, and increased residence time in the intestinal cavity |
Rats |
XIE, et al. [43] |
Association with of Liposomal Curcumin and its Metabolite Tetrahydrocurcumin: Two-hour infusion levels were higher than eight-hour, and would be preferable for liquid malignancies; however, eight-hour infusion would be preferable for solid tumors. |
Healthy Beagle Dogs |
HELSON, et al. [44] |
Association with Liposomal Curcumin and its Metabolite Tetrahydrocurcumin: Facilitate distribution and elevated tissue concentrations of curcumin may inhibit or saturate a putative reductase enzyme converting curcumin to THC |
Healthy Beagle Dogs |
MATABUDULm et al. [45] |
Ameliorates Nephrotoxicity: Decrease levels of serum creatinine and urea, renal malondialdehyde, NO, tumor necrosis factor-α with a concurrent increase in renal glutathione peroxidase and superoxide dismutase activities. Reduced cyclooxygenase-2 expression |
Methotrxate-induced Nephrotoxicity Rats |
MORSY, et al. [46] |
Ameliorates Nephrotoxicity: Decrease serum concentrations TNF-alpha, renal TNF-alpha, and decreased MCP-1 and ICAM-1 mRNA expression in kidney |
Cisplatin-induced Nephrotoxicity Mice |
SANDUR, et al. [47] |
Ameliorative Effect via Modulation of Inflammation, Oxidative Stress and Cell Death |
|
MENG, et al. [48] |
Apoptosis: Pathway PARP-, cleavage |
Pre-B Acute Lymphoblastic Leukemia Cell Lines |
MISHRA ,et al. [31] |
Apoptosis and Renoprotective effects: Inhibiting oxidative stress through regulation of the AMPK and Nrf2/HO-1 signaling pathways, ameliorated RM-associated renal injury |
Rhabdomyolysis-induced rats |
WU, et al. [49] |