Name: Induction of the Murine Subarachnoid Hemorrhage Model and Brain Slice Preparation for Fluorescent Imaging
Uploaded: 2023-08-18T15:00:00
Description: Watch this Scientific Journal Video about Induction of the Murine Subarachnoid Hemorrhage Model and Brain Slice Preparation for Fluorescent Imaging at JoVE.com

induction of the murine subarachnoid hemorrhage model and brain slice preparation for fluorescent imaging

تصور انقباض الدماغ pericyte بعد نزيف تحت العنكبوتية

Brain pericytes, distinguished by their slender protuberances and protruding cell bodies, encircle the microcirculation1,2. While cerebral blood flow augmentation is predominantly driven by capillary dilation, smaller arteries exhibit slower rates of dilation3. Pericyte contractility exerts influence over capillary diameter and pericyte morphology, impacting vascular dynamics4. Contraction of brain pericytes leads to capillary constriction, and in pathological scenarios, excessive contraction may impede erythrocyte flow5. Various factors, including norepinephrine released from the locus coeruleus, can induce brain pericyte contraction within capillaries6. With a regulatory role in cerebral blood flow, pericytes exhibit 20-HETE synthesis, serving as an oxygen sensor during hyperoxia7. Oxidative-nitrative stress-triggered contraction of brain pericytes detrimentally affects capillaries5. Despite both in vivo and ex vivo investigations into brain pericyte contraction8, limited knowledge persists regarding the imaging of viable and non-viable brain pericytes within brain slices.
Crucially, post-tissue fixation imaging of brain pericytes compromises their vitality and subsequent contractility assessment. Moreover, in scenarios such as neurological disorders (e.g., subarachnoid hemorrhage - SAH), transgenic labeling of brain pericytes fails to differentiate between viable and non-viable pericytes, as confirmed by our preliminary SAH-induced brain pericyte death study9. 
To surmount these challenges, we employed TO-PRO-3 to label live pericytes, while deceased ones were stained with propidium iodide (PI). We used high-resolution confocal imaging technologies to visualize viable and non-viable brain pericytes in brain slices while preserving slice activity during imaging. This article aims to present a reproducible method for imaging viable and non-viable brain pericytes in brain slices, serving as a valuable tool to probe the impact of brain pericytes on cerebral microcirculation post SAH.

تسليط الضوء على المؤلف: تصوير pericytes بعد نزيف تحت العنكبوتية في القوارض 

تصوير خلايا الدماغ الحيوية وغير الحيوية في شرائح الدماغ بعد النزف تحت العنكبوتية

Our study showed a significant increase in pericytes deaths. So starting at a sick horse after SAH, it demonstrated a positive correlation between the number of low vital parasites and the time elapsed after SAH. Imaging vital and the non-vital brain parasites in brain slices following SAH and the parasite isolation techniques, have advanced the research in my field.Currently, it's quite difficult to fully distinguish between dead parasites and dead endothelial cells. Our study find contraction-dependent apoptosis in parasites after SAH. We have developed a very reliable protocol, which enables the fluorescent labeling, both functional and a non-functional brain parasite in brain sections, and the same time.

Watch this Scientific Journal Video about Induction of the Murine Subarachnoid Hemorrhage Model and Brain Slice Preparation for Fluorescent Imaging at JoVE.com

Induction of the Murine Subarachnoid Hemorrhage Model and Brain Slice Preparation for Fluorescent Imaging  

تحريض نموذج النزف تحت العنكبوتية للفأر وإعداد شريحة الدماغ للتصوير الفلوري

لإنشاء النزف تحت العنكبوتية ، أو نموذج SAH ، أدخل إبرة حقن مجهرية في صهريج فوق سائل الفئران المخدر. باستخدام مضخة حقنة ، قم بحقن الدم الذاتي المكتسب من شريان ذيل الفئران في الصهريج فوق السيلار. الآن زرع إبرة أخرى في البطين الدماغي الجانبي الأيمن عند الإحداثيات المحددة.بالنسبة لنماذج SAH ، قم بحقن 0.2 ملليلتر من دم شريان ذيل الفئران. بالنسبة لمجموعات SHAM ، قم بحقن نفس الحجم من محلول ملحي متساوي التوتر. بعد قطع الرأس ، استخرج دماغ الفئران بالكامل وغمره في السائل الشوكي الدماغي الاصطناعي البارد أو ACSF.مع اهتزاز ، وإعداد شرائح الدماغ الحادة من 200 ميكرومتر والجليد البارد متوازن ACSF. ضع شرائح الدماغ على شبكة من النايلون ، مغمورة في ACSF متوازن في غرفة تخزين عند 35 إلى 37 درجة مئوية.

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