2018
DOI: 10.1002/ejp.1288
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Impaired chronic pain‐like behaviour and altered opioidergic system in the TASTPM mouse model of Alzheimer's disease

Abstract: This study shows attenuated pain-like behaviour in a transgenic mouse model of Alzheimer's disease due to alterations in the opioidergic system and central plasticity mechanisms of persistent pain.

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Cited by 21 publications
(18 citation statements)
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“… 7 , 59 , 67 , 94 , 99 , 105 , 133 , 137 A chemically induced model of osteoarthritis through an intra-articular injection of monosodium iodoacetate within transgenic TASTPM AD mice has provided insights into interactions between clinically relevant pain, neurodegenerative pathophysiology, and opioid analgesia. 4 , 5 TASTPM mice demonstrate an age-dependent reduction in thermal nociception that coincides with amyloid pathology in pain-related brain regions. 4 Naloxone, an opioid antagonist, restored thermal nociceptive thresholds to that of wild-type controls.…”
Section: Parkinson Diseasementioning
confidence: 96%
See 1 more Smart Citation
“… 7 , 59 , 67 , 94 , 99 , 105 , 133 , 137 A chemically induced model of osteoarthritis through an intra-articular injection of monosodium iodoacetate within transgenic TASTPM AD mice has provided insights into interactions between clinically relevant pain, neurodegenerative pathophysiology, and opioid analgesia. 4 , 5 TASTPM mice demonstrate an age-dependent reduction in thermal nociception that coincides with amyloid pathology in pain-related brain regions. 4 Naloxone, an opioid antagonist, restored thermal nociceptive thresholds to that of wild-type controls.…”
Section: Parkinson Diseasementioning
confidence: 96%
“…Subsequent administration of morphine not only produced an antinociceptive effect but also increased the noxious threshold significantly greater than that seen in wild-type animals. 5 Conversely, gabapentin showed no efficacy. Thus, altered processing within opioidergic circuitry may partially mediate altered pain processing as well as influence both efficacy and centrally mediated side effects of opioidergic pharmacotherapy.…”
Section: Parkinson Diseasementioning
confidence: 99%
“…Nurses can assess pain through a variety of pain assessment tools [18], but the quality and utility of these tools have been questioned [19][20][21]. Further, opioids are usually the first choice for analgesia at the end of life [22], but there is evidence that those with advanced dementia respond poorly to opioid treatment and experience more harmful side effects than people without dementia [22,23]. Since persons with dementia at the end of life find it difficult, or are unable, to self-report pain, many of the available pain assessment tools cannot be used [24].…”
Section: Introductionmentioning
confidence: 99%
“…Nurses can assess pain through a variety of pain assessment tools [15], but the quality and utility of these tools have been questioned [16][17][18]. Further, opioids are usually the first choice for analgesia at the end of life [19], but there is evidence that PWAD respond poorly to opioid treatment and experience more harmful side effects than people without dementia [19,20 ]. Since PWAD find it difficult, or are unable, to self-report pain, many of the available pain assessment tools cannot be used [21].…”
Section: Introductionmentioning
confidence: 99%