Transcriptional regulation of crystallin, redox, and apoptotic genes by C-Phycocyanin in the selenite-induced cataractogenic rat model

Mol Vis. 2015 Jan 14:21:26-39. eCollection 2015.

Abstract

Purpose: This study was designed to examine the constrictive potential of C-Phycocyanin (C-PC) in regulating changes imposed on gene expression in the selenite-induced cataract model.

Methods: Wistar rat pups were divided into three groups of eight each. On P10, Group I received an intraperitoneal injection of normal saline. Groups II and III received a subcutaneous injection of sodium selenite (19 μmol/kg bodyweight); Group III also received an intraperitoneal injection of C-PC (200 mg/kg bodyweight) on P9-14. Total RNA was isolated on P16, and the relative abundance of mRNA of the crystallin structural genes, redox components, and apoptotic cascade were ascertained with real-time PCR with reference to the internal control β-actin.

Results: Real-time PCR analysis showed the crystallin genes (αA-, βB1-, γD-) and redox cycle components (Cat, SOD-1, Gpx) were downregulated, the apoptotic components were upregulated, and antiapoptotic Bcl-2 was downregulated in Group II. Treatment with 200 mg/kg bodyweight C-PC (Group III) transcriptionally regulated the instability of the expression of these genes, thus ensuring C-PC is a prospective anticataractogenic agent that probably delays the onset and progression of cataractogenesis induced by sodium selenite.

Conclusions: C-PC treatment possibly prevented cataractogenesis triggered by sodium selenite, by regulating the lens crystallin, redox genes, and apoptotic cascade mRNA expression and thus maintains lens transparency. C-PC may be developed as a potential antioxidant compound applied in the future to prevent and treat age-related cataract.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Animals, Newborn
  • Catalase / genetics
  • Catalase / metabolism
  • Cataract / chemically induced
  • Cataract / genetics
  • Cataract / metabolism
  • Cataract / pathology
  • Cataract / prevention & control*
  • Crystallins / genetics
  • Crystallins / metabolism
  • Disease Models, Animal
  • Gene Expression Regulation / drug effects*
  • Glutathione Peroxidase / genetics
  • Glutathione Peroxidase / metabolism
  • Injections, Intraperitoneal
  • Lens, Crystalline / drug effects*
  • Lens, Crystalline / metabolism
  • Lens, Crystalline / pathology
  • Microtubule-Associated Proteins / genetics
  • Microtubule-Associated Proteins / metabolism
  • Phycocyanin / pharmacology*
  • Protective Agents / pharmacology*
  • Protein Isoforms / genetics
  • Protein Isoforms / metabolism
  • Proto-Oncogene Proteins c-bcl-2 / genetics
  • Proto-Oncogene Proteins c-bcl-2 / metabolism
  • RNA, Messenger / genetics*
  • RNA, Messenger / metabolism
  • Rats
  • Rats, Wistar
  • Selenious Acid
  • Superoxide Dismutase / genetics
  • Superoxide Dismutase / metabolism
  • Transcription, Genetic

Substances

  • Crystallins
  • Microtubule-Associated Proteins
  • Protective Agents
  • Protein Isoforms
  • Proto-Oncogene Proteins c-bcl-2
  • RNA, Messenger
  • cryaB protein, rat
  • Phycocyanin
  • Catalase
  • Glutathione Peroxidase
  • Superoxide Dismutase
  • Selenious Acid