Cannabidiol-Loaded Extracellular Vesicles from Human Umbilical Cord Mesenchymal Stem Cells Alleviate Paclitaxel-Induced Peripheral Neuropathy.
Anil Kumar KalvalaArvind BagdePeggy ArthurTanmay KulkarniSantanu BhattacharyaSunil SurapaneniNil Kumar PatelRamesh NimmaAragaw GebeyehuNagavendra KommineniDavid G MeckesLi SunBipika BanjaraKeb Mosley-KellumThanh Cong DinhMandip SinghPublished in: Pharmaceutics (2023)
In cancer patients, chronic paclitaxel (PTX) treatment causes excruciating pain, limiting its use in cancer chemotherapy. The neuroprotective potential of synthetic cannabidiol (CBD) and CBD formulated in extracellular vesicles (CBD-EVs) isolated from human umbilical cord derived mesenchymal stem cells was investigated in C57BL/6J mice with PTX-induced neuropathic pain (PIPN). The particle size of EVs and CBD-EVs, surface roughness, nanomechanical properties, stability, and release studies were all investigated. To develop neuropathy in mice, PTX (8 mg/kg, i.p.) was administered every other day (four doses). In terms of decreasing mechanical and thermal hypersensitivity, CBD-EVs treatment was superior to EVs treatment or CBD treatment alone ( p < 0.001). CBD and CBD-EVs significantly reduced mitochondrial dysfunction in dorsal root ganglions and spinal homogenates of PTX-treated animals by modulating the AMPK pathway ( p < 0.001). Studies inhibiting the AMPK and 5HT1A receptors found that CBD did not influence the neurobehavioral or mitochondrial function of PIPN. Based on these results, we hypothesize that CBD and CBD-EVs mitigated PIPN by modulating AMPK and mitochondrial function.
Keyphrases
- mesenchymal stem cells
- umbilical cord
- neuropathic pain
- spinal cord
- endothelial cells
- skeletal muscle
- signaling pathway
- spinal cord injury
- squamous cell carcinoma
- drug delivery
- stem cells
- high glucose
- oxidative stress
- combination therapy
- atomic force microscopy
- insulin resistance
- metabolic syndrome
- young adults
- subarachnoid hemorrhage
- risk assessment
- induced pluripotent stem cells
- blood brain barrier
- cancer therapy
- lymph node metastasis