Formulated Curcumin Prevents Paclitaxel-Induced Peripheral Neuropathy through Reduction in Neuroinflammation by Modulation of α7 Nicotinic Acetylcholine Receptors

被引:8
|
作者
Caillaud, Martial [1 ,2 ]
Thompson, Danielle [1 ]
Toma, Wisam [1 ]
White, Alyssa [1 ]
Mann, Jared [1 ]
Roberts, Jane L. [1 ]
Bigbee, John W. [3 ]
Gewirtz, David A. [4 ,5 ,6 ,7 ]
Damaj, M. Imad [1 ]
机构
[1] Virginia Commonwealth Univ, Dept Pharmacol & Toxicol, Translat Res Initiat Pain & Neuropathy, Med Coll Virginia Campus, Richmond, VA 23284 USA
[2] Nantes Univ, INSERM, Enter Nervous Syst Gut & Brain Disorders, IMAD, F-44000 Nantes, France
[3] Virginia Commonwealth Univ, Dept Anat & Neurobiol, Sch Med, Med Coll Virginia Campus, Richmond, VA 23284 USA
[4] Virginia Commonwealth Univ, Dept Pharmacol, Med Coll Virginia Campus, Richmond, VA 23284 USA
[5] Virginia Commonwealth Univ, Dept Toxicol, Med Coll Virginia Campus, Richmond, VA 23284 USA
[6] Virginia Commonwealth Univ, Dept Med, Med Coll Virginia Campus, Richmond, VA 23298 USA
[7] Virginia Commonwealth Univ, Massey Canc Ctr, Med Coll Virginia Campus, Richmond, VA 23284 USA
关键词
curcumin; chemotherapy; peripheral neuropathy; neuroinflammation; alpha 7 nACh receptors; OSTEOARTHRITIS; MERIVA(R); EFFICACY; SAFETY; TRIAL;
D O I
10.3390/pharmaceutics14061296
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Paclitaxel is widely used in the treatment of various types of solid malignancies. Paclitaxel-induced peripheral neuropathy (PIPN) is often characterized by burning pain, cold, and mechanical allodynia in patients. Currently, specific pharmacological treatments against PIPN are lacking. Curcumin, a polyphenol of Curcuma longa, shows antioxidant, anti-inflammatory, and neuroprotective effects and has recently shown efficacy in the mitigation of various peripheral neuropathies. Here, we tested, for the first time, the therapeutic effect of 1.5% dietary curcumin and Meriva (a lecithin formulation of curcumin) in preventing the development of PIPN in C57BL/6J mice. Curcumin or Meriva treatment was initiated one week before injection of paclitaxel and continued throughout the study (21 days). Mechanical and cold sensitivity as well as locomotion/motivation were tested by the von Frey, acetone, and wheel-running tests, respectively. Additionally, sensory-nerve-action-potential (SNAP) amplitude by caudal-nerve electrical stimulation, electronic microscopy of the sciatic nerve, and inflammatory-protein quantification in DRG and the spinal cord were measured. Interestingly, a higher concentration of curcumin was observed in the spinal cord with the Meriva diet than the curcumin diet. Our results showed that paclitaxel-induced mechanical hypersensitivity was partially prevented by the curcumin diet but completely prevented by Meriva. Both the urcumin diet and the Meriva diet completely prevented cold hypersensitivity, the reduction in SNAP amplitude and reduced mitochondrial pathology in sciatic nerves observed in paclitaxel-treated mice. Paclitaxel-induced inflammation in the spinal cord was also prevented by the Meriva diet. In addition, an increase in alpha 7 nAChRs mRNA, known for its anti-inflammatory effects, was also observed in the spinal cord with the Meriva diet in paclitaxel-treated mice. The use of the alpha 7 nAChR antagonist and alpha 7 nAChR KO mice showed, for the first time in vivo, that the anti-inflammatory effects of curcumin in peripheral neuropathy were mediated by these receptors. The results presented in this study represent an important advance in the understanding of the mechanism of action of curcumin in vivo. Taken together, our results show the therapeutic potential of curcumin in preventing the development of PIPN and further confirms the role of alpha 7 nAChRs in the anti-inflammatory effects of curcumin.
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页数:20
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