Abstract
Diabetic neuropathy is the most entrenched complication of diabetes. Usually, it affects the distal foot and toes, which then gradually approaches the lower part of the legs. Diabetic foot ulcer (DFU) could be one of the worst complications of diabetes mellitus. Long-term diabetes leads to hyperglycemia, which is the utmost contributor to neuropathic pain. Hyperglycemia causing an upregulation of voltage-gated sodium channels in the dorsal root ganglion (DRG) was often observed in models of neuropathic pain. DRG opening frequency increases intracellular sodium ion levels, which further causes increased calcium channel opening and stimulates other pathways leading to diabetic peripheral neuropathy (DPN). Currently, pain due to diabetic neuropathy is managed via antidepressants, opioids, gamma-aminobutyric acid (GABA) analogs, and topical agents such as capsaicin. Despite the availability of various treatment strategies, the percentage of patients achieving adequate pain relief remains low. Many factors contribute to this condition, such as lack of specificity and adverse effects such as light-headedness, languidness, and multiple daily doses. Therefore, nanotechnology outperforms in every aspect, providing several benefits compared to traditional therapy such as site-specific and targeted drug delivery. Nanotechnology is the branch of science that deals with the development of nanoscale materials and products, even smaller than 100 nm. Carriers can improve their efficacy with reduced side effects by incorporating drugs into the novel delivery systems. Thus, the utilization of nanotechnological approaches such as nanoparticles, polymeric nanoparticles, inorganic nanoparticles, lipid nanoparticles, gene therapy (siRNA and miRNA), and extracellular vesicles can extensively contribute to relieving neuropathic pain.
Highlights
Diabetes mellitus (DM) is a common metabolic disorder characterized by diabetic neuropathy, influencing around 90% of patients [1]
Many apparent mechanisms have been put forward to elucidate the pain related to diabetic neuropathy, including auto-oxidative stress, hyperglycemia, agitated polyol pathway, enhanced levels of advanced glycation end products (AGEs), and rise in protein kinase C (PKC)
dorsal root ganglion (DRG) consists of satellite glial cells (SGCs), which are mainly involved in the expression of the P2X4 receptor
Summary
Diabetes mellitus (DM) is a common metabolic disorder characterized by diabetic neuropathy, influencing around 90% of patients [1]. There are numerous therapeutic agents utilized in the treatment of DNP, half of the population is not able to achieve adequate pain relief This failure is not due to the lack of efficacy of the drug but due to inadequate drug delivery at the site of action [14]. DM rats, when treated with NONRATT021972 [long non-proteincoding RNAs (lncRNAs) siRNA], have shown that the expression of the DRG P2X3 receptor is significantly decreased as compared to type 2 diabetes mellitus (T2DM) rats in which no treatment is given. Baclofen-loaded PLGA nanoparticles enhanced the retention duration of drug in the brain in order to mitigate neuropathic pain and turned out to be a suitable carrier for baclofen [16] Another emerging technology involves ribonucleic acid interference (RNAi) that mainly blocks gene assertion after transcription. Novel approaches for targeting the DRG with the illustration of physiology of DRG and pathophysiology of DNP are discussed
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.