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Neurophysiological effects in cortico-basal ganglia-thalamic circuits of antidyskinetic treatment with 5-HT1A receptor biased agonists

Brys, Ivani (författare)
Lund University,Lunds universitet,Integrativ neurofysiologi,Forskargrupper vid Lunds universitet,Integrative Neurophysiology,Lund University Research Groups
Halje, Pär (författare)
Lund University,Lunds universitet,Integrativ neurofysiologi,Forskargrupper vid Lunds universitet,Integrative Neurophysiology,Lund University Research Groups
Scheffer-Teixeira, Robson (författare)
Federal University of Rio Grande do Norte
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Varney, Mark (författare)
Neurolixis Inc.
Newman-Tancredi, Adrian (författare)
Neurolixis Inc.
Petersson, Per (författare)
Umeå University,Lund University,Lunds universitet,Umeå universitet,Institutionen för integrativ medicinsk biologi (IMB),Integrative Neurophysiology and Neurotechnology, Neuronano Research Center, Department of Experimental Medical Sciences, Lund University, Sweden,Integrativ neurofysiologi,Forskargrupper vid Lunds universitet,Integrative Neurophysiology,Lund University Research Groups
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 (creator_code:org_t)
Elsevier BV, 2018
2018
Engelska.
Ingår i: Experimental Neurology. - : Elsevier BV. - 0014-4886 .- 1090-2430. ; 302, s. 155-168
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Recently, the biased and highly selective 5-HT1A agonists, NLX-112, F13714 and F15599, have been shown to alleviate dyskinesia in rodent and primate models of Parkinson's disease, while marginally interfering with antiparkinsonian effects of levodopa. To provide more detailed information on the processes underlying the alleviation of dyskinesia, we have here investigated changes in the spectral contents of local field potentials in cortico-basal ganglia-thalamic circuits following treatment with this novel group of 5-HT1A agonists or the prototypical agonist, 8-OH-DPAT. Dyskinetic symptoms were consistently associated with 80 Hz oscillations, which were efficaciously suppressed by all 5-HT1A agonists and reappeared upon co-administration of the antagonist, WAY100635. At the same time, the peak-frequency of fast 130 Hz gamma oscillations and their cross-frequency coupling to low-frequency delta oscillations were modified to a different extent by each of the 5-HT1A agonists. These findings suggest that the common antidyskinetic effects of these drugs may be chiefly attributable to a reversal of the brain state characterized by 80 Hz gamma oscillations, whereas the differential effects on fast gamma oscillations may reflect differences in pharmacological properties that might be of potential relevance for non-motor symptoms.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Neurologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Neurology (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Neurovetenskaper (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Neurosciences (hsv//eng)

Nyckelord

Systems neurophysiology
Parkinson's disease
Dyskinesia
6-OHDA rat
Oscillations
Local held tential
6-OHDA rat
Dyskinesia
Local field potential
Oscillations
Parkinson's disease
Systems neurophysiology

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