Prolidase activity in aqueous and serum samples of cataract cases with Pseudoexfoliation syndrome

Çalışkan B., Serhat Özaslan M., Aksoy M., Salman İ.

EXPERIMENTAL EYE RESEARCH, cilt.214, 2022 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 214
  • Basım Tarihi: 2022
  • Doi Numarası: 10.1016/j.exer.2021.108880
  • Dergi Adı: EXPERIMENTAL EYE RESEARCH
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, Academic Search Premier, BIOSIS, Chemical Abstracts Core, EMBASE, MEDLINE
  • Anahtar Kelimeler: Prolidase, Pseudoexfoliation syndrome, Etiopathogenesis, MATRIX METALLOPROTEINASES, DEPENDENT REGULATION, COLLAGEN, FIBROBLASTS, DEFICIENCY, INHIBITORS, PROLINE, LENS
  • Atatürk Üniversitesi Adresli: Evet

Özet

Pseudoexfoliation syndrome (PEX) represents an age-related systemic disease that is characterized by the accumulation of extracellular matrix material in ocular tissues and visceral organs. Abnormal matrix remodeling is thought to be one of the important factors in the etiopathogenesis of the disease. Prolidase represents an enzyme, which takes a significant part in collagen biosynthesis and remodeling of the extracellular matrix. The purpose of the current research was to assess the prolidase enzyme activity in the aqueous and serum samples of subjects with PEX. The study population consisted of 66 subjects, involving 33 subjects with age-related cataract among patients with PEX and 33 subjects with age-related cataract without PEX. The prolidase activity measurement was performed using the modified Chinard's method. Significantly increased aqueous prolidase activity was detected in the group with PEX (p 0.01). Despite about a three times higher increase in the serum prolidase activity of the group with PEX in comparison with the control group, the two groups did not differ statistically significantly (p 0.05). The high prolidase enzyme activity in the aqueous samples of subjects with PEX suggests that the collagen cycle and the remodeling of the extracellular matrix are accelerated. These results can be a guide for understanding the formation mechanisms of PEX.