AI Article Synopsis

  • Berberine (Ber) shows promise as a treatment for ulcerative colitis (UC) due to its anti-inflammatory properties, but its use is limited by poor water solubility and bioavailability.
  • Exosomes derived from human placental mesenchymal stem cells (HplMSC-Exos) are being explored as effective carriers for Ber, enhancing its delivery and targeting to the colon while maintaining low toxicity.
  • Engineered exosomes loaded with Ber (Exos-Ber) exhibit antioxidant and anti-inflammatory effects, promote cell repair, and may improve UC treatment by influencing the MAPK signaling pathway.

Article Abstract

Berberine (Ber), an isoquinoline alkaloid, is a potential drug therapy for ulcerative colitis (UC) because of its anti-inflammatory activity, high biological safety, and few side effects. Nevertheless, its clinical application is hindered by its limited water solubility and low bioavailability. Currently, compared to synthetic nanocarriers, exosomes as carriers possess advantages such as low toxicity, high stability, and high specificity. Human placental mesenchymal stem cell-derived exosomes (HplMSC-Exos) have emerged as a promising drug delivery system, offering intrinsic anti-inflammatory and antioxidant activities. Therefore, we engineered MSC-Exos loaded with Ber (Exos-Ber) to enhance the solubility and bioavailability of Ber and for colon targeting, revealing a novel approach for treating UC with natural compounds. Structurally and functionally, Exos-Ber closely resembled unmodified Exos. Both in vitro and in vivo investigations confirmed the antioxidant and anti-inflammatory properties of Exos-Ber. Notably, Exos-Ber exhibited reparative effects on injured epithelial cells and reduced cellular apoptosis. Furthermore, Exos-Ber concurrently demonstrated anti-inflammatory and antioxidant activities, contributing to the mitigation of UC, possibly through its modulation of the MAPK signaling pathway. Overall, our findings demonstrate the potential of Exos-Ber as a promising therapeutic option for alleviating UC, highlighting its capacity to enhance the clinical applicability of Ber.

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Source
http://dx.doi.org/10.1016/j.jcis.2024.05.162DOI Listing

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