Abstract

Aim. To study the level of activity of lysosomal cysteine proteases (cathepsins H, B, L) in blood plasma and fractionated leukocytes (polymorphonuclear and mononuclear) in patients with Alzheimer’s disease in comparison with similar indicators in persons without signs of neurodegeneration as a possible marker of Alzheimer’s disease development and diagnosis. Materials and methods. The spectrofluorimetric study of cathepsins B, L, H activity level in plasma and fractionated leukocytes was conducted in 22 patients diagnosed with Alzheimer’s disease in comparison with the same indicators in 22 patients matched by sex, age and associated diseases with patients of the observation group, but having no signs of neurodegeneration. Results. The activity of all three enzymes, and especially cathepsin H, increased significantly in blood plasma. A significant increase is also noted in the activity of cathepsins H, B, and L in homogenates of fractionated leukocytes. At the same time, in both polymorphonuclear and mononuclear leukocytes the greatest degree of changes is demonstrated by the activity of cathepsin B, and the least is the activity of cathepsin L. Given the available data on an increased cathepsin B activity in the cerebrospinal fluid of patients with Alzheimer’s disease, we can assume a correlation between the state of lysosomal proteases activity in the Central nervous system and in the peripheral blood cells. Conclusion. Alzheimer’s disease is associated with increased activity of cysteine cathepsins in plasma, polymorphonuclear and mononuclear leukocytes of peripheral blood, which can be considered as one of the possible markers of development and diagnosis of the disease.

Highlights

  • The activity of all three enzymes, and especially cathepsin H, increased significantly in blood plasma

  • A significant increase is noted in the activity of cathepsins H, B, and L in homogenates of fractionated leukocytes

  • In both polymorphonuclear and mononuclear leukocytes the greatest degree of changes is demonstrated by the activity of cathepsin B, and the least is the activity of cathepsin L

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Summary

ОРИГИНАЛЬНЫЕ СТАТЬИ

Изучить уровень активности лизосомальных цистеиновых протеиназ (катепсинов H, B, L) в плазме крови и фракционированных лейкоцитах (полиморфноядерных и моноядерных) пациентов с болезнью Альцгеймера в сравнении с аналогичными показателями у лиц, не имеющих признаков нейродегенерации, как возможный маркер развития и диагностики болезни Альцгеймера. В гомогенатах фракционированных лейкоцитов также отмечается статистически значимое повышение активности катепсинов Н, B, L, при этом как в полиморфноядерных, так и в моноядерных лейкоцитах в наибольшей степени изменяется активность катепсина В, наименьшей –катепсина L. Болезнь Альцгеймера ассоциирована с нарастанием активности цистеиновых катепсинов в плазме, полиморфноядерных и моноядерных лейкоцитах периферической крови, что может рассматриваться как один из возможных маркеров развития и диагностики заболевания. Изменение активности лизосомальных цистеиновых протеаз плазмы, моноядерных и полиморфноядерных лейкоцитов крови при болезни Альцгеймера.

Изменение активности лизосомальных цистеиновых протеаз
Materials and methods
Results
Conclusion
Оригинальные статьи
МАТЕРИАЛЫ И МЕТОДЫ
РЕЗУЛЬТАТЫ И ОБСУЖДЕНИЕ
Сведения об авторах
Full Text
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