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

Author:

Kalvala Anil1ORCID,Bagde Arvind1,Arthur Peggy1,Kulkarni Tanmay2ORCID,Bhattacharya Santanu23,Surapaneni Sunil1,Patel Nil1,Nimma Ramesh1,Gebeyehu Aragaw1,Kommineni Nagavendra1ORCID,Li Yan4ORCID,Meckes David5,Sun Li5ORCID,Banjara Bipika1ORCID,Mosley-Kellum Keb1,Dinh Thanh1,Singh Mandip1ORCID

Affiliation:

1. Department of Pharmaceutics, College of Pharmacy and Pharmaceutical Sciences, Florida A&M University, Tallahassee, FL 32301, USA

2. Department of Biochemistry and Molecular Biology, Mayo College of Medicine and Science, Jacksonville, FL 32224, USA

3. Department of Physiology and Biomedical Engineering, Mayo College of Medicine and Science, Jacksonville, FL 32224, USA

4. College of Engineering, Florida A&M University-Florida State University, 2525 Pottsdamer St., Tallahassee, FL 32310, USA

5. Department of Biomedical Sciences, Florida State University College of Medicine, 1115 West Call Street, Tallahassee, FL 32301, USA

Abstract

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.

Funder

Consortium for Medical Marijuana Clinical Outcomes Research

National Institute on Minority Health and Health Disparities of National Institutes of Health

NSF-CREST Center for Complex Materials Design for Multidimensional Additive Processing

Publisher

MDPI AG

Subject

Pharmaceutical Science

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