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Structural Biology 2018

Volume: 4

Biochemistry & Molecular Biology Journal

Page 58

March 15-16 2018

Barcelona, Spain

10

th

Edition of International Conference on

Structural Biology

A

mong the diseases of the blood, thalassemia occupies

a special place, associated with a reduction or complete

absence of synthesis of globin chains of hemoglobin. Azerbaijan

is considered as an endemic zone of these inherited blood

diseases, which makes conducted researches relevant. The aim

of this work was to study the relationship between the thiol status

of blood and the secretion of endogenous antimicrobial peptides.

The blood of 57 patients aged 6-17 years was studied. All patients

dependingon thepathologyweredivided intothe followinggroups:

group I-20 children with a homozygous form of

β

-thalassemia,

group II-37 children with G6PD deficiency. To assess the degree

of oxidative stress of the body, carbonylated proteins (CP) and

thiol status (TS) of blood were chosen as markers. To assess

the level of secretion of endogenous antimicrobial peptides, a

quantitative analysis of defensin and endotoxin in blood plasma

was performed using the ELISA method. The research was

carried out with the financial support of the Science Development

Foundation of Azerbaijan. As a result of research, it was revealed

that in group I patients, the amount of CP increased by 11%, in the

group II patients CP increased by 1.6% and TS decreased by 1.5%.

The level of defensin in group I increased by 2%, and endotoxin

by 1.7%. In group II, these indicators increased by 1.7% and 2.3%,

respectively. With the change of the body’s TS, the secretion

of

α

-defensin was increasing. In

β

-thalassemia, carbonylated

proteins increase in the blood, thiol status decreases, which

indicates at the increase of the influence of oxidative stress

associated with frequent infectious complications and activation

of neutrophils.

gulib18@mail.ru

Influence of the oxidative stress on the secretion of the

endogenous antimicrobial peptides in hereditary blood diseases

Azizova G I, Dadasheva A R

and

Efendiyev A M

Azerbaijan Medical University, Azerbaijan

Biochem Mol biol J, Volume 4

DOI: 10.21767/2471-8084-C1-009