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XXII. BIOCHEMICKÝ ZJAZD - Jesseniova lekárska fakulta

XXII. BIOCHEMICKÝ ZJAZD - Jesseniova lekárska fakulta

XXII. BIOCHEMICKÝ ZJAZD - Jesseniova lekárska fakulta

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Posters<br />

2.<br />

IS IT POSSIBLE TO IMPROVE DEMYELINATION DISEASES MONITORING BY<br />

DETERMINATION OF SOME ENZYME ACTIVITIES CHaraCTERISTIC FOR<br />

THE CENTraL NErvOUS SYSTEM?<br />

Monika Ďurfinová 1 , Marta Brechtlová 1 , Ľubica Procházková 2 , Peter Kukumberg 2 ,<br />

Ľubomír Kuračka 1 and Branislav Líška 1<br />

1<br />

Department of Chemistry, Biochemistry and Clinical Biochemistry, LF UK Bratislava,<br />

2<br />

2 nd Department of Neurology, LF UK Bratislava<br />

Multiple sclerosis (MS) is a chronic inflammatory disease of the central nervous system<br />

(CNS). It is the most common neurological disease characterized by recurrent relapses<br />

and/or progression that are attributable to multifocal inflammation, demyelination and<br />

axonal pathology within the CNS. MS lesions are typically located in the periventricular<br />

white matter of the brain as well as in superficial areas of the spinal cord. Since MS<br />

lesions are not routinely biopsied, the cerebrospinal fluid (CSF) is used for measurements<br />

of various soluble markers. We have started determination of enzyme activities<br />

in the CSF of MS patients, which have some relationship to the function of the CNS<br />

tissue – phosphodiesterase 3 , ,5 , -cAMP and K + -paranitrophenyl-phosphatase. These<br />

enzyme activities were at first monitored in model experiments in vitro. We suppose<br />

that K + -paranitrophenylphosphatase might have a connection with the nerve impulse<br />

transmission. Interestingly, the part of phosphodiesterase 3 , ,5 , -cAMP activity, which is<br />

calcium-calmodulin dependent, was inhibited by the conditions of activated oxidative<br />

stress. However, several questions still remain to be elucidated, e.g.: if this CNS inflamatory<br />

damage could infuence releasing of these enzymes into CSF and if these enzymes<br />

can reflect the intensity of the patological process.<br />

116 <strong>XXII</strong>. Biochemistry Congress, Martin

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