Cannabidiol-Loaded Extracellular Vesicles from Human Umbilical Cord Mesenchymal Stem Cells Alleviate Paclitaxel-Induced Peripheral Neuropathy

被引:16
作者
Kalvala, Anil Kumar [1 ]
Bagde, Arvind [1 ]
Arthur, Peggy [1 ]
Kulkarni, Tanmay [2 ]
Bhattacharya, Santanu [2 ,3 ]
Surapaneni, Sunil [1 ]
Patel, Nil Kumar [1 ]
Nimma, Ramesh [1 ]
Gebeyehu, Aragaw [1 ]
Kommineni, Nagavendra [1 ]
Meckes Jr, David G. [4 ]
Sun, Li [4 ]
Banjara, Bipika [1 ]
Mosley-Kellum, Keb [1 ]
Dinh, Thanh Cong [1 ]
Singh, Mandip [1 ]
机构
[1] Florida A&M Univ, Coll Pharm & Pharmaceut Sci, Dept Pharmaceut, Tallahassee, FL 32301 USA
[2] Mayo Coll Med & Sci, Dept Biochem & Mol Biol, Jacksonville, FL 32224 USA
[3] Mayo Coll Med & Sci, Dept Physiol & Biomed Engn, Jacksonville, FL 32224 USA
[4] Florida State Univ, Dept Biomed Sci, Coll Med, 1115 West Call St, Tallahassee, FL 32301 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
extracellular vesicles; hUCMSCs; CBD-EVs; AMPK; atomic force microscopy; morphology; Young's modulus; NF-KAPPA-B; MITOCHONDRIAL BIOGENESIS; BREAST-CANCER; IN-VIVO; CHEMOTHERAPY; ACTIVATION; RECEPTORS; EXOSOMES; NANOPARTICLES; MECHANISMS;
D O I
10.3390/pharmaceutics15020554
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
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.
引用
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页数:24
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