2003) that precludes specific measurement
of cold allodynia symptoms. Hence, our menthol testing needs validation against a testing method that provides an objective evaluation of cold allodynia/parasthesia, preferably the gold standard of CS, such as quantitative sensory testing. The validation of the menthol testing using quantitative sensory tests will be one of the important future studies. In addition, although our healthy subjects Inhibitors,research,lifescience,medical and chemotherapy-naïve patients were similar in age, sex, and baseline CDTs, having colon cancer patients as controls rather than healthy volunteers would have established equivalency at baseline by accounting for the potential influence of cancer-specific changes on CDTs. Future studies would benefit from conducting additional evaluations of CDTs after oxaliplatin infusion, performing quantitative Inhibitors,research,lifescience,medical sensory testing, and using patients with colon cancer without OPN as controls. The present data show that menthol may be used to determine and evaluate the http://www.selleckchem.com/products/Y-27632.html neurotoxicity severity score, although the methodology using menthol has not been firmly established. Interestingly,
patients with prior oxaliplatin exposure had significantly elevated CDT at Inhibitors,research,lifescience,medical baseline, and patients with grade 3 neurotoxicity did not show significant changes in the CDT before and after oxaliplatin administration. These findings suggest that TRM8 may be associated with the chronic stage of OPN. Unfortunately, in this study, these patients were not Inhibitors,research,lifescience,medical prospectively monitored for changes in the CDT during and after a long period of oxaliplatin
treatment therefore, we could not confirm whether or not the CDT increased with OPN progression. A prospective, multicenter, randomized, double-blind Inhibitors,research,lifescience,medical study is needed to investigate the possibility of CDT as a diagnostic marker for OPN. In conclusion, our findings indicate that OPN may be associated with TRPM8 in acute hypersensitivity to CS, and that additional studies on TRPM8 will enhance our understanding of the mechanisms of OPN. Further, our study demonstrates the feasibility of undertaking CDT test in a clinical setting to facilitate the identification of early neurotoxicity, although larger Phosphatidylinositol diacylglycerol-lyase trials need to be conducted to confirm our findings. Acknowledgments Our heartfelt condolences and appreciation go to J. Iwamoto whose comments and suggestions were invaluable for our study. The assistance of K. Lee with manuscript preparation is gratefully acknowledged. The first two authors, T. Kono and M. Satomi, contributed equally to this work.
Cervical carotid artery stenosis (CS) is diagnosed using a combination of history, clinical examination, and imaging. Rapid advancement of noninvasive imaging modalities notwithstanding, biplane and rotational digital subtraction angiography still provide unsurpassed anatomic resolution of the endoluminal aspect of CS.