Synaptic control of motoneuronal excitability
Movement, the fundamental component of behavior and the principal extrinsic action of the
brain, is produced when skeletal muscles contract and relax in response to patterns of action …
brain, is produced when skeletal muscles contract and relax in response to patterns of action …
Update on the glutamatergic neurotransmitter system and the role of excitotoxicity in amyotrophic lateral sclerosis
PR Heath, PJ Shaw - Muscle & Nerve: Official Journal of the …, 2002 - Wiley Online Library
Excitotoxicity may play a role in certain disorders of the motor system thought to be caused
by environmentally acquired toxins, including lathyrism and domoic acid poisoning. Motor …
by environmentally acquired toxins, including lathyrism and domoic acid poisoning. Motor …
C9ORF72 repeat expansion causes vulnerability of motor neurons to Ca2+-permeable AMPA receptor-mediated excitotoxicity
Mutations in C9ORF72 are the most common cause of familial amyotrophic lateral sclerosis
(ALS). Here, through a combination of RNA-Seq and electrophysiological studies on …
(ALS). Here, through a combination of RNA-Seq and electrophysiological studies on …
AMPA exposures induce mitochondrial Ca2+ overload and ROS generation in spinal motor neurons in vitro
SG Carriedo, SL Sensi, HZ Yin… - Journal of …, 2000 - Soc Neuroscience
The reason for the selective vulnerability of motor neurons in amyotrophic lateral sclerosis
(ALS) is primarily unknown. A possible factor is the expression by motor neurons of Ca2+ …
(ALS) is primarily unknown. A possible factor is the expression by motor neurons of Ca2+ …
Glutamate, excitotoxicity and amyotrophic lateral sclerosis
The “glutamate hypothesis” is one of three major pathophysiological mechanisms of motor
neurone injury towards which current research effort into amyotrophic lateral sclerosis (ALS) …
neurone injury towards which current research effort into amyotrophic lateral sclerosis (ALS) …
ALS-linked Cu/Zn–SOD mutation increases vulnerability of motor neurons to excitotoxicity by a mechanism involving increased oxidative stress and perturbed calcium …
II Kruman, WA Pedersen, JE Springer… - Experimental neurology, 1999 - Elsevier
We employed a mouse model of ALS, in which overexpression of a familial ALS-linked
Cu/Zn–SOD mutation leads to progressive MN loss and a clinical phenotype remarkably …
Cu/Zn–SOD mutation leads to progressive MN loss and a clinical phenotype remarkably …
Oxidative stress and motor neurone disease
MR Cookson, PJ Shaw - Brain pathology, 1999 - Wiley Online Library
The effects of oxidative stress within post mitotic cells such as neurones may be cumulative,
and injury by free radical species is a major potential cause of the age‐related deterioration …
and injury by free radical species is a major potential cause of the age‐related deterioration …
Calcium‐permeable α‐amino‐3‐hydroxy‐5‐methyl‐4‐isoxazole propionic acid receptors: A molecular determinant of selective vulnerability in amyotrophic lateral …
TL Williams, NC Day, PG Ince… - Annals of Neurology …, 1997 - Wiley Online Library
The cause of the selective degeneration of motor neurons in amyotrophic lateral sclerosis
(ALS) remains unexplained. One potential pathogenetic mechanism is chronic toxicity due to …
(ALS) remains unexplained. One potential pathogenetic mechanism is chronic toxicity due to …
Mitochondrial involvement in amyotrophic lateral sclerosis
The causes of motor neuron death in amyotrophic lateral sclerosis (ALS) are so far
unknown. The involvement of mitochondria in the disease was initially suggested by …
unknown. The involvement of mitochondria in the disease was initially suggested by …
Synaptic restoration by cAMP/PKA drives activity-dependent neuroprotection to motoneurons in ALS
M Bączyk, NO Alami, N Delestrée, C Martinot… - Journal of Experimental …, 2020 - rupress.org
Excessive excitation is hypothesized to cause motoneuron (MN) degeneration in
amyotrophic lateral sclerosis (ALS), but actual proof of hyperexcitation in vivo is missing, and …
amyotrophic lateral sclerosis (ALS), but actual proof of hyperexcitation in vivo is missing, and …