Diabetes impairs synaptic plasticity in the superior cervical ganglion: Possible role for BDNF and oxidative stress

Journal of Molecular Neuroscience

Volumn 51, Issue 3, 2013, Pages 763-770

  Alzoubi, K H ^a   Khabour, O F ^a   Alhaidar, I A ^b   Aleisa, A M ^c   Alkadhi, K A ^b  

^a JORDAN UNIVERSITY OF SCIENCE AND TECHNOLOGY   (Jordan)

^b UNIVERSITY OF HOUSTON   (United States)

^c KING SAUD UNIVERSITY   (Saudi Arabia)

Author keywords

Basal synaptic transmission; BDNF; LTD; LTP; Oxidative stress; PTP

Indexed keywords

BRAIN DERIVED NEUROTROPHIC FACTOR; CATALASE; GLUTATHIONE; GLUTATHIONE DISULFIDE; GLUTATHIONE PEROXIDASE; GLUTATHIONE REDUCTASE; STREPTOZOCIN; THIOBARBITURIC ACID REACTIVE SUBSTANCE;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CONTROLLED STUDY; DIABETES MELLITUS; LONG TERM POTENTIATION; MALE; NERVE CELL PLASTICITY; NONHUMAN; OXIDATIVE STRESS; PERIPHERAL NERVOUS SYSTEM; RAT; SUPERIOR CERVICAL GANGLION; SYMPATHETIC GANGLION; SYNAPTIC TRANSMISSION;

ANIMALIA; RATTUS;

ACTION POTENTIALS; ANIMALS; BRAIN-DERIVED NEUROTROPHIC FACTOR; DIABETES MELLITUS, EXPERIMENTAL; GLUTATHIONE; LONG-TERM POTENTIATION; MALE; OXIDATIVE STRESS; RATS; RATS, WISTAR; SUPERIOR CERVICAL GANGLION;

EID: 84885947500     PISSN: 08958696     EISSN: 15591166     Source Type: Journal    
DOI: 10.1007/s12031-013-0061-1     Document Type: Article

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