Ischemia and status epilepitcus result in enhanced phosphorylation of calcium and calmodulin-stimulated protein kinase II on threonine 253

• Published in: Brain research 2008-07, Vol.1218, p.158-165
• Main Authors: Gurd, James W, Rawof, Salma, Zhen Huo, Jeanne, Dykstra, Crystal, Bissoon, Nankie, Teves, Lucy, Wallace, M. Christopher, Rostas, John A.P
• Format: Article
• Language: English
• Subjects: Animals; Biological and medical sciences; Calcium - metabolism; Calcium and calmodulin-dependent protein kinase II; Calcium-Calmodulin-Dependent Protein Kinase Type 2 - metabolism; Disease Models, Animal; Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy; Ischemia; Ischemia - metabolism; Ischemia - pathology; Lithium Chloride; Male; Medical sciences; Nervous system (semeiology, syndromes); Neurology; Phosphorylation; Pilocarpine; Postsynaptic density; Prosencephalon - ultrastructure; Rats; Rats, Wistar; Status epilepticus; Status Epilepticus - chemically induced; Status Epilepticus - metabolism; Status Epilepticus - pathology; Synaptosomes - metabolism; Threonine - metabolism; Vascular diseases and vascular malformations of the nervous system
• ISSN: 0006-8993; 1872-6240
• DOI: 10.1016/j.brainres.2008.04.040

Abstract Ca2+ -stimulated protein kinase II (CaMKII) is critically involved in the regulation of synaptic function and is implicated in the neuropathology associated with ischemia and status epilepticus (SE). The activity and localization of CaMKII is regulated by multi-site phosphorylation. In the present study we investigated the effects of global ischemia followed by reperfusion and of SE on the phosphorylation of CaMKII on T253 in rat forebrains and compared this to the phosphorylation of T286. Both ischemia and SE resulted in marked increases in the phosphorylation of T253, and this was particularly marked in the postsynaptic density (PSD). Phosphorylation of T286 decreased rapidly towards basal levels following ischemia whereas phosphorylation of T253 remained elevated for between 1 and 6 h before decreasing to control values. Following SE, phosphorylation of T253 remained elevated for between 1 and 3 h before decreasing to control levels. In contrast, phosphorylation of T286 remained elevated for at least 24 h following the termination of SE. Total CaMKII associated with PSDs transiently increased 10 min following ischemia, but only several hours following SE. The results demonstrate that phoshorylation of CaMKII on T253 is enhanced following both ischemia/reperfusion and SE and indicate that the phosphorylation of T253 and T286 are differentially regulated.