Academic Journal

Abstract TP94: Combined Chlorpromazine and Promethazine Induce Neuroprotective Hibernation Without Hypothermia in Experimental Stroke

التفاصيل البيبلوغرافية
العنوان: Abstract TP94: Combined Chlorpromazine and Promethazine Induce Neuroprotective Hibernation Without Hypothermia in Experimental Stroke
المؤلفون: Geng, Xiaokun, Stone, Christopher R, DeGracia, Donald, Ding, Yuchuan
المصدر: Stroke ; volume 49, issue Suppl_1 ; ISSN 0039-2499 1524-4628
بيانات النشر: Ovid Technologies (Wolters Kluwer Health)
سنة النشر: 2018
الوصف: Introduction: Hibernation, in which the lowering of metabolism and body temperature reduces the energetic needs of brain cells, has emerged as a frontier in the search for neuroprotective agents against ischemia. In fact, it has been partially achieved clinically with therapeutic hypothermia. Metabolically slowed, hibernation-like states lead to a decrease in ischemic damage and improved neurologic outcomes. However, decreasing body temperature can cause serious systemic complications. Thus, finding ways to induce a hibernation-like drop in metabolism without also inducing hypothermia is clinically important. It was shown that pharmacological hibernation with Chlorpromazine and Promethazine (C+P) resulted in decreased brain activity and decreased body temperature. Here, by isolating these two effects, and by investigating effects on NADPH oxidase (NOX), the key component in the pathway most central to oxidative injury during ischemia, we sought to determine whether the neuroprotective effect of C+P is dependent or independent from its effect on body temperature. Methods: Sprague-Dawley rats were subjected to 2h MCAO, and 6 or 24 h reperfusion, upon which rats received an IP injection of saline or C+P (8 mg/kg). Temperature was maintained at 37°C, or allowed to spontaneously change. Infarct volumes and neurological deficits were examined. Oxidative stress was determined by levels of ATP, lactate, NADH and reactive oxygen species (ROS). NOX activity and expression of NOX subunits (p47 phox , gp91 phox , p22 phox and p67 phox ) were measured at 6 and 24 h reperfusion. Results: In 2 h MCAO rats, body temperatures were significantly reduced by 1 0 C after C+P within 5 min. At 2 h, body temperatures reached 34 0 C and remained significantly low for up to 6 h. Following 6 and 24 h of reperfusion, C+P decreased infarct volume, neurological deficit, lactate and ROS levels, but increased ATP and NADH. NOX activity and subunit expressions were down-regulated. C+P-induced neuroprotection was not affected by maintaining ...
نوع الوثيقة: article in journal/newspaper
اللغة: English
DOI: 10.1161/str.49.suppl_1.tp94
الاتاحة: http://dx.doi.org/10.1161/str.49.suppl_1.tp94
http://journals.lww.com/00007670-201801001-00455
رقم الانضمام: edsbas.CD7B7005
قاعدة البيانات: BASE
الوصف
DOI:10.1161/str.49.suppl_1.tp94