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MacKinnon-Booth, N.

Publications and source records attributed to MacKinnon-Booth, N..

3 recordsLinked to original sources

Machine learning behavioral analysis reveals cervical instability as an early biomarker of Amyotrophic Lateral Sclerosis

Early detection of neuromuscular disorders is a major clinical challenge, with most diagnoses only occurring after considerable motor neuron degeneration has already taken place. The central problem for early diagnosis of neuromuscular diseases is the subtlety of early symptoms and where to look for them. Without defined behavioral markers, the earliest stages of disease go undetected, delaying intervention and limiting neuroprotective therapeutic evaluation. Here, we present a machine learning (ML) based framework that identifies subtle postural alterations in freely behaving animals. Using longitudinal pose data from SOD1G93A mice, a widely used Amyotrophic Lateral Sclerosis (ALS) mouse model, we focused on postural states in idle periods, behavioral states usually overlooked in disease monitoring. Our analyses revealed consistent deviations in posture and a feature analysis pinpointed cervical instability during adolescence as a key distinguishing feature. We validated these findings through two independent behavioral assays engaging cervical musculature: rearing and wet-dog shakes, both of which showed significant impairments in male SOD1G93A mice as early as 3 weeks of age, many weeks earlier than conventional muscle function assays. This approach establishes an unbiased, non-invasive, scalable strategy for detecting early-stage neuromuscular dysfunction, and provides a foundation both for clinical behavioral biomarker development in ALS and related disorders and will enable evaluation of early neuroprotective interventions.

neuroscience↗

Injured SSTR2+ nociceptor axons in neuromas drive chronic spontaneous neuropathic pain

Spontaneous pain is a common but poorly understood consequence of peripheral nerve injury1-3, including injuries that lead to the formation of neuromas4,5. We developed a chronic neuroma model for measuring spontaneous pain-related behaviours in mice, which revealed that limb flicks - emerging predominantly 2 months post-injury - reflect spontaneous paroxysmal pain. Ectopic activity of injured dorsal root ganglia (DRG) sensory neurons whose axonal endings terminate within the neuroma drives this spontaneous pain. In vivo imaging showed that a subset of small-diameter DRG sensory neurons are the source of spontaneous neural signals emanating from the neuroma, and these spontaneously active neurons are distinct from the intact larger diameter sensory neurons that mediate stimulus-evoked mechanical allodynia from spared nerves. Cell-type-specific gain- and loss-of-function studies identified a genetically- and functionally-defined subtype of small-diameter C-fibre nociceptors whose injured axons in neuromas drive spontaneous limb flicks/neuropathic pain. These findings establish the neurobiological basis of spontaneous pain enabling targeted pain management strategies and define a cellular and mechanistic separation between spontaneous and evoked neuropathic pain.

neuroscience↗

Selective modification of ascending spinal outputs in acute and neuropathic pain states

Pain hypersensitivity arises from the plasticity of peripheral and spinal somatosensory neurons, which modifies nociceptive input to the brain and alters pain perception. We utilized chronic calcium imaging of spinal dorsal horn neurons to determine how the representation of somatosensory stimuli in the anterolateral tract, the principal pathway transmitting nociceptive signals to the brain, changes between distinct pain states. In healthy conditions, we identify stable, narrowly tuned outputs selective for cooling or warming, and a neuronal ensemble activated by intense/noxious thermal and mechanical stimuli. Induction of an acute peripheral sensitization with capsaicin selectively and transiently retunes nociceptive output neurons to encode low-intensity stimuli. In contrast, peripheral nerve injury-induced neuropathic pain results in a persistent suppression of innocuous spinal outputs coupled with activation of a normally silent population of high-threshold neurons. These results demonstrate the differential modulation of specific spinal outputs to the brain during nociceptive and neuropathic pain states.

neuroscience↗