Pedro Miranda

Dr. Pedro Miranda


Research Focus & Metrics

Academic Career Length

15Years (2012-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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28 November 2012 in BMC Complementary and Alternative Medicine
Verified
Journal Article
Open access
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IJIsela Juarez-Rojop
Isela Juarez-Rojop
JDJuan Diaz-Zagoya
Juan Diaz-Zagoya
JBJorge Ble-Castillo
Jorge Ble-Castillo
PMPedro Miranda
Pedro Miranda
ACAndrés Eliú Castell-Rodríguez
Andrés Eliú Castell-Rodríguez
DBDeysi Y Bermúdez-Ocaña
Deysi Y Bermúdez-Ocaña
Traditional plant treatment for diabetes has shown a surging interest in the last few decades. Therefore, the purpose of this study was to assess the hypoglycemic effect of the aqueous extract of C. papaya leaves in diabetic rats. Several studies have reported that some parts of the C. papaya plant exert hypoglycemic effects in both animals and humans.

PMPedro Miranda
Pedro Miranda
ACAndrés Eliú Castell-Rodríguez
Andrés Eliú Castell-Rodríguez
JVJuan Vargas-Mancilla
Juan Vargas-Mancilla
Carlos Alfonso Tovilla-ZárateCarlos Alfonso Tovilla-Zárate
Carlos Alfonso Tovilla-Zárate
JBJorge Ble-Castillo
Jorge Ble-Castillo
JDJuan Diaz-Zagoya
Juan Diaz-Zagoya
The aim of the present study was to investigate the effect of C. papaya L. leaf extract (CPLE) on pancreatic islets in streptozotocin (STZ)-induced diabetic rats, as well as on cultured normal pancreatic cells with STZ in the medium. CPLE (3–125 mg/Kg) was administered orally for 20 days, while a group of diabetic rats received 5 IU/Kg/day of insulin. At the end of the treatment the rats were sacrificed. Blood was obtained to assess glucose and insulin levels. The pancreas was dissected to evaluate β cells by immunohistochemistry. In addition, normal pancreatic cells were cultured in a medium that included CPLE (3–12 mg). One half of the cultured cells received simultaneously CPLE and STZ (6 mg), while the other half received CPLE and five days later the STZ. After three days of incubation, insulin was assayed in the incubation medium. The CPLE administered to diabetic rats improved the fasting glycemia and preserved the number and structure of pancreatic islets. However, when CPLE was added to pancreatic cells in culture along with STZ, the insulin concentration was higher in comparison with the cells that only received STZ. In conclusion, the CPLE preserves the integrity of pancreatic islets, improves the basal insulin secretion and protects cultured cells from the adverse effects of STZ.