2004
DOI: 10.1523/jneurosci.3698-04.2004
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Conversion of the Modulatory Actions of Dopamine on Spinal Reflexes from Depression to Facilitation in D3Receptor Knock-Out Mice

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Cited by 104 publications
(78 citation statements)
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References 64 publications
(73 reference statements)
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“…This was in spite of the fact that D 1 and D 2 receptor agonists reduced evoked polysynaptic potentials as predicted by previous reports (Clemens and Hochman 2004). This suggests that transmission from propriospinal relay interneurons in the sacral cord to the lumbar CPG was not affected.…”
Section: Monoaminergic Depression Of Rhythmic Activitysupporting
confidence: 85%
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“…This was in spite of the fact that D 1 and D 2 receptor agonists reduced evoked polysynaptic potentials as predicted by previous reports (Clemens and Hochman 2004). This suggests that transmission from propriospinal relay interneurons in the sacral cord to the lumbar CPG was not affected.…”
Section: Monoaminergic Depression Of Rhythmic Activitysupporting
confidence: 85%
“…DA has been observed to cross react with ␣ 2 receptors in other parts of the brain (Cornil et al 2002), and paracrine release of DA within the dorsal horn could potentially activate neighboring synapses (Mundorf et al 2001;Ridet et al 1993). One issue is that our DA bath concentrations were high, and concentration-dependent effects on evoked reflexes have been reported in the 10-to 20-M range using a mouse spinal cord preparation (Clemens and Hochman 2004). Nevertheless, it does not detract from our observations that direct activation of DA receptors does not suppress cauda equina evoked locomotor-like activity.…”
Section: Monoaminergic Depression Of Rhythmic Activitymentioning
confidence: 98%
“…Moreover, the disinhibition of IML leads to an increase in sympathetic output that might explain the alteration of ANS observed by some authors [11,29]. In addition, there is wide evidence that the dopaminergic system dysfunction induces hypertension [30][31][32], as supported by experimental studies in dopamine D3 knockout mice that has been proposed as a potential animal model for RLS [33].…”
Section: Tablementioning
confidence: 97%
“…Clemens et al (2006) suggested a decreased D3R-mediated inhibition of spinal sensory and reflex circuits as a pathogenetic concept in RLS (Clemens et al, 2006). This is supported by the switch from inhibitory to excitatory dopamine effects on spinal reflexes in D3RϪ/Ϫ mice (Clemens and Hochman, 2004) that resembles the increased excitability of the flexor reflex detected in RLS patients (Bara-Jimenez et al, 2000). Additionally, the most commonly and successfully used dopamine agonists have a relevant if not predominant D 3 agonism.…”
Section: Introductionmentioning
confidence: 97%