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Time-Dependent Memory and Gait Improvement by Intranasally-Administered Extracellular Vesicles in Parkinson’s Disease Model Rats

  • Karīna Narbute*
  • , Vladimirs Piļipenko
  • , Jolanta Pupure
  • , Toms Klinovičs
  • , Jānis Auders
  • , Ugnė Jonavičė
  • , Karolina Kriaučiūnaitė
  • , Augustas Pivoriunas
  • , Vija Kluša
  • *Šī darba korespondējošais autors
  • University of Latvia
  • State Research Institute Centre for Innovative Medicine

Zinātniskās darbības rezultāts: Devums žurnālamZinātniskais raksts (žurnālā)koleģiāli recenzēts

20 Atsauces (Scopus)

Kopsavilkums

We have recently demonstrated that extracellular vesicles (EVs) derived from the human teeth stem cells improve motor symptoms and normalize tyrosine hydroxylase (TH) expression in the nigrostriatal structures of Parkinson’s disease (PD) model rats obtained by 6-hydroxydopamine (6-OHDA) unilateral injection into the medial forebrain bundle (MFB). The aim of this study was to clarify: (1) how long therapeutic effects persist after discontinuation of 17-day intranasal administration of EVs in 6-OHDA rats; (2) may EVs reverse cognitive (learning/memory) dysfunction in these PD model rats; (3) whether and how the behavioral improvement may be related to the expression of TH and Nissl bodies count in the nigrostriatal structures. Our results demonstrated that in 6-OHDA rats, gait was normalized even ten days after discontinuation of EVs administration. EVs successfully reversed 6-OHDA-induced impairment in spatial learning/memory performance; however, the beneficial effect was shorter (up to post-treatment day 6) than that revealed for gait improvement. The shorter effect of EVs coincided with both full normalization of TH expression and Nissl bodies count in the nigrostriatal structures, while slight but significant increase in the 6-OHDA-decreased Nissl count persisted in the substantia nigra even on the post-treatment day 20, supposedly due to the continuation of protein synthesis in the living cells. The obtained data indicate the usefulness of further studies to find the optimal administration regimen which could be translated into clinical trials on PD patients, as well as to clarify other—apart from dopaminergic—neuromodulatory pathways involved in the EVs mechanism of action.

OriģinālvalodaAngļu
Lapas (no-līdz)605-613
Lapu skaits9
ŽurnālsCellular and Molecular Neurobiology
Sējums41
Izdevuma numurs3
DOIs
Publikācijas statussPublicēts - apr. 2021

OECD Zinātnes nozare

  • 3. Medicīnas un veselības zinātnes

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