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Successful Pre-Clinical Management of Irinotecan-Debilitated Animals: A Protein- Based Accessory Phytomedicine

Authors :
Nylane M. N. Alencar
Márcio V. Ramos
Gisele F. P. Rangel
Luana D. do Carmo
Liviane M. A. Rabelo
Alfredo A. V. Silva
Tamiris F. G. de Sousa
Roberto C. P. Lima Júnior
Deysi V. T. Wong
Renata F. C. Leitão
Pedro J. C. Magalhães
Brandon F. Sousa
Marisa J. S. Frederico
Source :
Anti-cancer agents in medicinal chemistry. 22(18)
Publication Year :
2022

Abstract

Background: Calotropis procera is a laticiferous plant (Apocynaceae) found in tropical regions all over the world. The ultrastructural characteristics of laticifers, their restricted distribution among different taxonomic groups, and in some species in each clade, as peptidases from latex, make them very attractive for biological analysis. Objective: The study aims to investigate the effects of LP-PII-IAA (laticifer protein (LP) sub-fraction II (PII) of C. procera presenting an iodoacetamide-inhibited cysteine proteinase activity) on irinotecan-induced intestinal mucositis, a serious adverse effect of this medicine for the treatment of cancer. Methods: LP-PII-IAA is composed of closely related isoforms (90%) of peptidases derived from catalysis and an osmotin protein (5%). Animals receiving co-administration of LP-PII-IAA presented a significant decrease in mortality, absence of diarrhea, histological preservation, and normalization of intestinal functions. Results: Clinical homeostasis was accompanied by a reduction in MPO activity and declined levels of IL-1β, IL-6 and KC, while the IL-10 level increased in LP-PII-IAA-treated animals. COX-2 and NF-kB immunostaining was reduced and the levels of oxidative markers (GSH, MDA) were normalized in animals that received LP-PII-IAA. Conclusion: We suggest that peptidases from the latex of Calotropis procera were instrumental in the suppression of the adverse clinical and physiological effects of irinotecan.

Details

ISSN :
18755992
Volume :
22
Issue :
18
Database :
OpenAIRE
Journal :
Anti-cancer agents in medicinal chemistry
Accession number :
edsair.doi.dedup.....760fb7724d14c6d6db2a964f0e1e236c