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

Author:

Ramos Márcio V.1ORCID,Alencar Nylane M. N.2,Rangel Gisele F. P.2,do Carmo Luana D.2,Rabelo Liviane M. A.2,Silva Alfredo A. V.2,de Sousa Tamiris F. G.2,Lima Júnior Roberto C. P.2,Wong Deysi V. T.2,Leitão Renata F. C.2,Magalhães Pedro J. C.2,Sousa Brandon F.1,Frederico Marisa J. S.2

Affiliation:

1. Departamento de Bioquímica e Biologia Molecular, Federal University of Ceara, Campus do Pici. Fortaleza, Ceará, Brazil

2. Departamento de Fisiologia e Farmacologia, Federal University of Ceara, Campus do Porangabuçú. Fortaleza, Ceará, Brazil

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.

Publisher

Bentham Science Publishers Ltd.

Subject

Cancer Research,Pharmacology,Molecular Medicine

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