scholarly journals Pharmacological correction of morphofunctional retinal injury using 11-amino acid fragment of darbepoetin in the experiment

2019 ◽  
Vol 5 (3) ◽  
pp. 43-55
Author(s):  
Victoria O. Gubareva ◽  
Anton L. Pazhinsky ◽  
Sergey S. Lugovskoy ◽  
Elizaveta Yu. Dubovtsova ◽  
Daria S. Vain ◽  
...  

Introduction: The retinoprotective effect of the 11-amino acid fragment of darbepoetin PRK-002 on the models of hypertensive retinal angiopathy and hypertensive neuroretinopathy in Wistar rats was investigated in comparison with carbamylated darbepoetin and sulodexide. Materials and methods: The protective effects of the pharmacological agents were assessed using the following criteria: a semi-quantitative assessment of changes in the eye fundus when performing ophthalmoscopy, the retinal blood flow, the b/a coefficient, eNOs expression in retinal vessels, specific number of neuronal nuclei in the inner nuclear layer, and p53 expression in the retina. Results and discussion: A pronounced protective effect, exceeding sulodexide at a dose of 150 LRU/kg and carbamylated darbepoetin at a dose of 300 μg/kg when correcting retinal angiopathy was observed in PRK-002 at a dose of 4 µg/kg, which expressed in adjustment of the retinal vessels’ calibers, removing retinal arterio-venous crossings, reaching the target levels of the retinal microcirculation, the b/a coefficient, and the restoration of eNOs expression in the endothelium of retinal vessels. PRK-002 at a dose of 4 µg/kg has a pronounced neuroprotective effect comparable to carbamylated darbepoetin at a dose of 300 µg/kg in correction of hypertensive neuroretinopathy, which expressed in the normalization of the fundus image, reaching the b/a target values, the specific number of neuronal nuclei in the inner nuclear layer, inhibition of p53 expression in the neurons of the inner nuclear and ganglionic layers. Conclusion: The study revealed angio- and neuroprotective activity of the 11-amino acid fragment of darbepoetin PRK-002 in correction of retinal injury formed on the background of hypertension.

2004 ◽  
Vol 11 (6) ◽  
pp. 531-532
Author(s):  
C. A. Staton ◽  
N. J. Brown ◽  
G. Rodgers ◽  
K. P. Corke ◽  
S. Tazzyman ◽  
...  

Endocrinology ◽  
1996 ◽  
Vol 137 (11) ◽  
pp. 5182-5185 ◽  
Author(s):  
W K Samson ◽  
T C Murphy ◽  
D Robison ◽  
T Vargas ◽  
E Tau ◽  
...  

2018 ◽  
Vol 16 (33) ◽  
pp. 5987-5998 ◽  
Author(s):  
Danil P. Zarezin ◽  
Olga I. Shmatova ◽  
Valentine G. Nenajdenko

Chiral β3-isocyanopropionic acids derivatives is a new type of isocyanides for multicomponent reactions. The use of these isocyanides in Ugi and Passerini reactions allows to prepare short peptides and depsipeptides with β-amino acid moiety in the structure.


Peptides ◽  
2013 ◽  
Vol 45 ◽  
pp. 78-84 ◽  
Author(s):  
Andre L.A. Souza ◽  
Paola Díaz-Dellavalle ◽  
Andrea Cabrera ◽  
Patricia Larrañaga ◽  
Marco Dalla-Rizza ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document