Objective To investigate the effect of intraspinal grafting of adenovirus- mediated BDNF ex vivo transgene myoblasts and GM- 1 gangliosides on N- methyl- D- aspartate (NMDA) receptors after spinal cord injury (SCI) in rats.
Effect of intraspinal grafting of adenovirus- mediated BDNF ex vivo transgene myoblasts and GM- 1 gangliosides on N- methyl- D- aspartate (NMDA) receptors after cervical spinal cord contusion in rats
Objective: To investigate the effects of dextromethorphan (DM) which is an antitussive and a N-methyl-D-aspartate (NMDA) receptor antagonist as well. It is intramuscularly (I.M.) injected in perioperative period, reduces pain and decreases the requirements of opioid analgesic after radical mastectomy (RM).
Objective To investigate the effect of intraspinal grafting of adenovirus- mediated BDNF ex vivo transgene myoblasts and GM- 1 gangliosides on N- methyl- D- aspartate (NMDA) receptors after spinal cord injury (SCI) in rats.
Effect of intraspinal grafting of adenovirus- mediated BDNF ex vivo transgene myoblasts and GM- 1 gangliosides on N- methyl- D- aspartate (NMDA) receptors after cervical spinal cord contusion in rats
Objective: To investigate the effects of dextromethorphan (DM) which is an antitussive and a N-methyl-D-aspartate (NMDA) receptor antagonist as well. It is intramuscularly (I.M.) injected in perioperative period, reduces pain and decreases the requirements of opioid analgesic after radical mastectomy (RM).
(2) Reginal water and ion contents of rat spinal cord tissue were measured with the atomic absorption spectrophotometry after administering intrathecally different dosage of 3-(2-carboxypiperazin-4-yl)-propyl-l-phosphonic acid (CPP),a specific antagonist of N-methyl-D-aspartate (NMDA) receptor,to rats at 48 h posttrauma.
Effect of intraspinal grafting of adenovirus-mediated BDNF ex vivo transgene myoblasts cells and methylprednisolone on N-methyl-D-aspartate(NMDA) receptors after cervical spinal cord contusion in rats
Ketamine is an antagonist of glutamate N-methyl-d-aspartate receptors (NMDA-R) which takes effect on the PCP site of NMDA-R. As a non-competitive antagonist, its effects can not be reversed even by high dose of NMDA or glutamic (Glu).
Abstract The protective effect of D-AP7 (D-(-)-2-Amino-7-Phosphono-heptanoic Acid). a specific antagonist of N-Methyl-D-Aspartate (NMDA) receptor, was evaluated in cat with traumatic brain edema D-AP7 (15μg/kg) was administered through cisterma cerebellomedullaris. 20 min after head injury in one group (n=9).
The effects of intracerebroventricular (icv) agonists and antagonists of N-methyl-D-aspartate (NMDA) and alpha-amino-3-hydroxy-5-methyl-4-isoxazole-propionic acid (AMPA) receptors on the general anesthesia of propofol were studied.
Activation of rat cerebellum granule cells by N-methyl-D-aspartate (NMDA, 10-4-10-3 M) results in progressive increase in reactive oxygen species (ROS) and suppression of the ouabain-sensitive part of Na/K-ATPase activity.
Objective: To study the effect of glycine site/NMDA (N-methyl-D-aspartate) receptor antagonist MRZ2/576 on the conditioned place preference (CPP) and locomotor activity induced by morphine in mice.
Background and purpose A low-affinity, use-dependent N-Methyl-D-Aspartate (NMDA) antagonist AR-R15896AR has neuroprotective properties in animal models of ischaemic stroke.
Abstract The protective effect of D-AP7 (D-(-)-2-Amino-7-Phosphono-heptanoic Acid).a specific antagonist of N-Methyl-D-Aspartate (NMDA) receptor, was evaluated in cat with traumatic brain edema D-AP7 (15μg/kg) was administered through cisterma cerebellomedullaris. 20 min after head injury in one group (n=9).treated with artificial cerebrospinal fluid in another group (ACSF,n=9) and same operation (n=9) controls.After 6 hours all cats were sac...
In the present study,Sprague-Dawley rats were subjected to traumatic spinal cord injury using Allen's method.At different periods posttrauma:(1) Reginal concentrations of excitatory amino acid (EAA) were assessed with high-performance liquid chromatography;(2) Reginal water and ion contents of rat spinal cord tissue were measured with the atomic absorption spectrophotometry after administering intrathecally different dosage of 3-(2-carboxypiperazin-4-yl)-propyl-l-phosphonic acid (CPP...