Guavira Fruit Pomace Promotes Immunomodulation and Reduction of Tumor Growth in Walker 256 Tumor-Bearing Rats

Author:

Zulin Natália Eirão1,Martins Carolina Garcia2,Appel Márcia Helena3,da Silva Coutinho Débora Salles4,Bialli Amanda Plaça1,Bronoski Daiana Milena1,Carvalhal Stephanie Rubianne Silva1,dos Santos Elisvania Freitas5,Loubet Filho Paulo Sérgio56,Bonatto Sandro José Ribeiro1,Fernandes Luiz Cláudio1,Cordeiro Lucimara Mach Côrtes4,Iagher Fabíola1

Affiliation:

1. Department of Physiology, Division of Biological Sciences, Federal University of Parana, Curitiba, PR, Brazil

2. Instituto de Pesquisa Pelé Pequeno Príncipe, Curitiba, PR, Brazil

3. Department of Structural Biology, Molecular and Genetics, State University of Ponta Grossa, Ponta Grossa, PR, Brazil

4. Department of Biochemistry and Molecular Biology, Federal University of Parana, Curitiba, PR, Brazil

5. Faculty of Pharmaceutical Sciences, Food, and Nutrition, Federal University of Mato Grosso do Sul, Campo Grande, MS, Brazil

6. Department of Food Science and Nutrition, School of Food Engineering, State University of Campinas, Campinas, SP, Brazil

Abstract

Background: Guavira fruit is widely used for juice extraction purposes, and this process generates large amounts of pomace (waste). Guavira pomace was dried and milled to produce guavira pomace flour (GPF), which is rich in antioxidants and dietary fibers (polysaccharides). These compounds are known for their immunomodulatory and antitumor effects. Objective: To investigate whether GPF intake promotes immunomodulation and reduces Walker 256 tumor growth in rats. Methods: GPF was provided to Wistar rats in two different models: 1) 15-day Model, according to which, Walker 256 tumor-bearing rats received GPF (63 mg/200 g b.w./day) simultaneously to tumor growth for 15 days; 2) 45-day Model, according to which, tumor-bearing rats received GPF for 30 days before tumor cell implantation, as well as during tumor growth - it totaled 45 days. After animals were euthanized, tumors were collected and weighed, and tumor cells were isolated for proliferation capacity determination ex vivo. Enzymatic/colorimetric methods were used to determine resident peritoneal macrophages’ functionality, whereas blood T and B lymphocytes were assayed for proliferation capacity, ex vivo, under stimuli Results: The 15-day Model did not show tumor mass or cell proliferation reduction in the treated group. GPF stimulated macrophage response in tumor-bearing and non-tumor-bearing rats. However, there was a substantial reduction in tumor mass and tumor cell proliferation under the 45-day Model. Macrophage and lymphocyte response decreased; it suggested that GPF can directly act in the tumor. Conclusion: Based on these findings, GPF has immunomodulatory and antitumor actions, and ingestion time plays a key role in them.

Publisher

Bentham Science Publishers Ltd.

Subject

Public Health, Environmental and Occupational Health,Nutrition and Dietetics,Food Science

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