نعترف المساعدة الماهرة من آني B. كريستنسن، إليزابيث V. أندرسن، بليندا B. Bringtoft ومقدمي الرعاية الحيوانية في وزارة الطب التجريبي، كوبنهاجن الحرم الجامعي، كلية الصحة والعلوم الطبية، جامعة كوبنهاغن، الدنمارك. يعقوب Lønholdt وشكره على مساعدته التقنية الممتازة في تصوير إجراءات. وأيد هذه الدراسة في جزء من مركز LIFEPHARM لفي الجسم الحي الصيدلة وجامعة كوبنهاغن.

تم تنفيذ الإجراءات الموضحة وفقا لبروتوكولات وافق عليها الدنماركية الحيوان التجريب التفتيش تحت إشراف وزارة الأغذية والزراعة ومصايد الأسماك. 1. الدم أخذ العينات من الصافن الجانبي أو عظم الكعب الوريد <ol style=";text-align:right;direction:rtl"><li style=";text-align:right;direction:rtl"> تنفيذ هذا الإجراء دون تخدير ومساعدة من محقق واحد، واحد التعامل مع خنزير غينيا، واحد جمع العينة. </li><li style=";text-align:right;direction:rtl"> حلق منطقة الجفن من الساق الخلفية مع ماكينة حلاقة كهربائية حتى عروق مرئية. ضمان مساحة كبيرة بما فيه الكفاية لتجنب التدخل الفراء مع موقع الثقب. </li><li style=";text-align:right;direction:rtl"> وضع الساق الخلفية في حمام الماء الفاتر وفرك بلطف الساق، مما يجعل من الأوردة المتوسعة وأكثر وضوحا. </li><li style=";text-align:right;direction:rtl"> مسح الساق مع منشفة نظيفة وتطهير الموقع ثقب بشاش أو قطعة من القطن المبلل الكحول 70٪. </li><li style=";text-align:right;direction:rtl"> كبح خنزير غينيا وتمديد الساق الخلفية إلى الأسفل أثناء تطبيق ضغط لطيف على الفور فوق الركبة ر مشتركس توفير ركود. </li><li style=";text-align:right;direction:rtl"> ثقب الوريد باستخدام إبرة 21 G أو انسيت. جمع مثل الدم، باستخدام مجموعة أو أنبوب شعري. التعامل بلطف الساق للمساعدة في تدفق الدم. </li><li style=";text-align:right;direction:rtl"> الافراج عن ركود، بمجرد الحصول على العينة. تطبيق قطعة من الشاش أو القطن والصوف مع ضغط لطيف على الموقع ثقب حتى توقف النزيف. </li><li style=";text-align:right;direction:rtl"> عودة الحيوان إلى قفصه ورصد لمدة 5-10 دقيقة لضمان الارقاء. </li></ol> 2. أخذ عينات الدم من الوريد الأذن <ol style=";text-align:right;direction:rtl"><li style=";text-align:right;direction:rtl"> تنفيذ هذا الإجراء دون تخدير إما وحدها أو يفضل مع مساعدة من زميل واحد. </li><li style=";text-align:right;direction:rtl"> تطهير السطح الظهري للأذن باستخدام الشاش أو قطعة من القطن المبلل الكحول 70٪. </li><li style=";text-align:right;direction:rtl"> تطبيق الضغط الخفيف على قاعدة الأذن لتوفير ركود. </li><li style=";text-align:right;direction:rtl"> ثقب الوريد باستخدام إبرة أو مشرط 21 G، وجمع الدم. </li><li style=";text-align:right;direction:rtl"> الافراج عن ركود، بمجرد الحصول على العينة، تطبيق قطعة من الشاش أو القطن والصوف مع جنرال الكتريكتوقف الضغط ntle الى موقع ثقب حتى النزيف. </li><li style=";text-align:right;direction:rtl"> عودة الحيوان إلى قفصه ورصد لمدة 5-10 دقيقة لضمان الارقاء. </li></ol> 3. الدم أخذ العينات من الوريد الوداجي <ol style=";text-align:right;direction:rtl"><li style=";text-align:right;direction:rtl"> تنفيذ هذا الإجراء باستخدام مساعدة من محقق إضافي واحد؛ التعامل مع الخنازير الغينية واحد وجمع العينة. </li><li style=";text-align:right;direction:rtl"> تخدير خنزير غينيا مع مخدر مناسبة لكامل مدة هذا الإجراء. مزيج من تلييتامين (0.93 ملغ / كلغ)، zolazepam (0.93 ملغ / كلغ)، زيلازين (1.49 ملغ / كلغ) وبوتورفانول (0.06 ملغ / كلغ) يمكن استخدامها. </li><li style=";text-align:right;direction:rtl"> وضع خنزير غينيا مخدرة على ظهرها وسحب بلطف اليدين نحو caudally. </li><li style=";text-align:right;direction:rtl"> يحلق وتطهير (على سبيل المثال، مع 70٪ كحول) الجزء البطني من الرقبة. </li><li style=";text-align:right;direction:rtl"> معطف الحقنة مع إما الهيبارين أو EDTA قبل أخذ العينات من أجل الحد من مخاطر تخثر. </li><li style=";text-align:right;direction:rtl"> جس الترقوة وإدراج G 25 (أو 23 G) إبرة شنت على 1 مل حقنة ا ف بتقريبية 1 سم الوحشي على خط الوسط على مستوى مفصل الكتف. الحفاظ على حقنة في زاوية تصاعدية وسطي طفيفة أثناء تطبيق ضغط سلبي طفيف. تجنب إتلاف الهياكل ويقع الوريد الوداجي سطحية جدا. إمالة الرقبة من خنزير غينيا إلى الوراء قليلا لتوفير ركود زيادة الوريد. </li><li style=";text-align:right;direction:rtl"> الافراج عن الأرجل الأمامية عندما يتم الحصول على عينة من الدم، والتخفيف من حدة الركود قبل سحب الإبرة. استخدام قطعة جافة من الشاش أو القطن والصوف لتطبيق ضغط لطيف على الموقع ثقب. </li><li style=";text-align:right;direction:rtl"> عودة الحيوان إلى قفص الانتعاش ورصد لضمان الارقاء والتعافي من التخدير. </li></ol>

<ol>
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K., Halliwell, B. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=High+fat+diets+and+pathology+in+the+guinea+pig+Atherosclerosis+or+liver+damage.">High fat diets and pathology in the guinea pig Atherosclerosis or liver damage.</a> Biochim Biophys Acta. 1832 (2), 355-364 (2013).</li><li>Tveden-Nyborg, P., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Maternal+vitamin+C+deficiency+during+pregnancy+persistently+impairs+hippocampal+neurogenesis+in+offspring+of+guinea+pigs.">Maternal vitamin C deficiency during pregnancy persistently impairs hippocampal neurogenesis in offspring of guinea pigs.</a> PLoS One. 7 (10), 12-18391 (2012).</li><li>Schjoldager, J. G., Tveden-Nyborg, P., Lykkesfeldt, J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Prolonged+maternal+vitamin+C+deficiency+overrides+preferential+fetal+ascorbate+transport+but+does+not+influence+perinatal+survival+in+guinea+pigs.">Prolonged maternal vitamin C deficiency overrides preferential fetal ascorbate transport but does not influence perinatal survival in guinea pigs.</a> Br J Nutr. 110 (9), 1573-1579 (2013).</li><li>Greulich, S., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Secretory+products+of+guinea+pig+epicardial+fat+induce+insulin+resistance+and+impair+primary+adult+rat+cardiomyocyte+function.">Secretory products of guinea pig epicardial fat induce insulin resistance and impair primary adult rat cardiomyocyte function.</a> J Cell Mol Med. 15 (11), 2399-2410 (2011).</li><li>Swifka, J., Weiss, J., Addicks, K., Eckel, J., Rosen, P. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Epicardial+fat+from+guinea+pig+a+model+to+study+the+paracrine+network+of+interactions+between+epicardial+fat+and+myocardium.">Epicardial fat from guinea pig a model to study the paracrine network of interactions between epicardial fat and myocardium.</a> Cardiovasc Drugs Ther. 22 (2), 107-114 (2008).</li><li>Pilny, A. 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A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=A+novel+anaesthetic+regimen+for+surgical+procedures+in+guinea+pigs.">A novel anaesthetic regimen for surgical procedures in guinea pigs.</a> Lab Anim. 35 (3), 271-276 (2001).</li><li>Saha, J. K., Xia, J., Grondin, J. M., Engle, S. K., Jakubowski, J. A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Acute+hyperglycemia+induced+by+ketamine+xylazine+anesthesia+in+rats+mechanisms+and+implications+for+preclinical+models.">Acute hyperglycemia induced by ketamine xylazine anesthesia in rats mechanisms and implications for preclinical models.</a> Exp Biol Med(Maywood). 230 (10), 777-784 (2005).</li></ol>

الكتاب ليس لديهم ما يكشف. تمت الموافقة على جميع الإجراءات بموجب قانون التجارب على الحيوانات من الدنمارك، وهو ما يتفق مع اتفاقية مجلس أوروبا ETS 123.

بالمقارنة مع الفئران والجرذان والخنازير الغينية هي مخيفة بطبيعتها ويجب أن اقتربت بهدوء والتعامل معها بشكل صحيح من أجل الحد من التوتر. من نقطة الرفق بالحيوان نظر، يتصرف بحذر هو بطبيعة الحال على سبيل الأولوية؛ ومع ذلك، وهذا أيضا يقلل من خطر الآثار المصاحبة للقلق على ا...

خنزير غينيا هو نموذج حيوانات التجارب قيما والتحقق من صحتها بسبب وجود عدد من أوجه التشابه البيولوجية للإنسان مثل شرط وجود امدادات الغذائية من فيتامين C، البروتين الدهني البلازما مقارنة تأييض البروتين الدهني الانزيمات وملامح، وكذلك أوجه الشبه المشتركة مع المشيمة البشرية و وضع ما قبل الولادة 1-3،7،8. هذا يجعل خنزير غينيا نموذج جذاب ومناسب لدراسة آثار الأمراض المرتبطة الحمية مثل مرض غير الكحولية الكبد الدهني وأمراض القلب والأوعية الدموية والآثار المفترضة من نقص فيتامين C ولكن أيضا تأثير على سبيل المثال، التدخل الغذائي الأمهات في البلدان النامية ذرية. وغالبا ما يتطلب أخذ عينات الدم المتكررة في كل من المدى القصير والطويل في الدراسات المجراة. بسبب الاختلافات التشريحية أنواع محددة من تعديل أسلوب أخذ العينات ضروري من أجل الحصول على عينات من الدم في خنازير غينيا بالمقارنة مع نماذج القوارض الأخرى <sup&gt; 4،5. ويشمل هذا الاختلاف في مجرى الأوردة والشرايين، وأيضا أن الخنازير الغينية ليس لها ذيل، وبالتالي لديها متطلبات وخيارات مختلفة لكلا أخذ العينات والتعامل معها. أخذ العينات من الوريد الصافن أو الرصغي، يدفع الحد الأدنى من الراحة والإجهاد في الحيوان و لا يتطلب التخدير 3،9. هذه التقنية تسمح تكرار عينات من كميات صغيرة من الدم (100-400 ميكرولتر)، على سبيل المثال، لتحديد العلامات الكيميائية الحيوية في البلازما. إذا كان حجم أصغر عينة كافية (50-100 ميكرولتر)، وهذا يمكن بسهولة الحصول عليها عن طريق الوريد ثقب الأذن. ويمكن أيضا أن تتم هذه التقنية في الحيوانات واعية ومفيد على سبيل المثال عند قياس مستوى السكر في الدم 10،11. أخذ العينات من حبل الوريد تسمح لجمع كميات أكبر من الدم (1-2 مل) ولكنها تتطلب التخدير. هنا، نقدم أربع تقنيات مختلفة لأخذ عينات الدم إما واعية أو مخدرة خنازير غينيا. بروكedures يتم توفير جميع الإجراءات غير الطرفية التي أحجام العينة وعدد العينات لا تتجاوز المبادئ التوجيهية لجمع الدم في الحيوانات المختبرية 6. هو في مصلحة العلم الجيد وكذلك الرفق بالحيوان أن الإجهاد يجب أن تبقى إلى أدنى حد ممكن. بالتالي، فقط المدربين تدريبا جيدا والشخصية المختصة أن تؤدي الإجراءات الحيوانية.

<table border="0" cellpadding="0" cellspacing="0" width="944">
	<tbody>
		<tr height="21">
			<td height="21" style="height:21px;width:216px;">Name of Material/ Equipment</td>
			<td style="width:295px;">Company</td>
			<td style="width:119px;">Catalog Number</td>
			<td style="width:315px;">Comments/Description</td>
		</tr>
		<tr height="20">
			<td height="20" style="height:20px;width:216px;">Electric shaver</td>
			<td style="width:295px;">Wella (Contura), Denmark</td>
			<td style="width:119px;">273207</td>
			<td>Alternative product may be used. Multiple suppliers</td>
		</tr>
		<tr height="20">
			<td height="20" style="height:20px;width:216px;">Syringes&#160;</td>
			<td style="width:295px;">B.Braun-Omnifix-F, Germany</td>
			<td style="width:119px;">9161406V</td>
			<td>Alternative product may be used. Multiple suppliers</td>
		</tr>
		<tr height="20">
			<td height="20" style="height:20px;width:216px;">Needles</td>
			<td style="width:295px;">BD Microlance,Spain</td>
			<td style="width:119px;">301156</td>
			<td>Alternative product may be used. Multiple suppliers</td>
		</tr>
		<tr height="20">
			<td height="20" style="height:20px;width:216px;">Microvette collection tube&#160;</td>
			<td style="width:295px;">Sarstedt, D-51588N&#252;mbrecht, Germany</td>
			<td style="width:119px;">201,288,100</td>
			<td>Alternative product may be used. Multiple suppliers</td>
		</tr>
		<tr height="20">
			<td height="20" style="height:20px;width:216px;">Accu-Check analyzer</td>
			<td style="width:295px;">Roche A/S Diagnostics, Denmark</td>
			<td style="width:119px;"></td>
			<td>Alternative product may be used. Multiple suppliers</td>
		</tr>
		<tr height="20">
			<td height="20" style="height:20px;width:216px;">Heparin 5000 IE/ml</td>
			<td style="width:295px;">LEO Pharma, Denmark</td>
			<td style="width:119px;"></td>
			<td>Alternative product may be used. Multiple suppliers</td>
		</tr>
		<tr height="20">
			<td height="20" style="height:20px;width:216px;">Anesthesia</td>
			<td style="width:295px;">Zoletil 50, Chemvet, Denmark</td>
			<td style="width:119px;"></td>
			<td>Alternative product may be used. Multiple suppliers</td>
		</tr>
		<tr height="20">
			<td height="20" style="height:20px;width:216px;">Anesthesia</td>
			<td style="width:295px;">Narcoxyl vet 20 mg/ml, Intervet, Denmark</td>
			<td style="width:119px;"></td>
			<td>Alternative product may be used. Multiple suppliers</td>
		</tr>
		<tr height="20">
			<td height="20" style="height:20px;width:216px;">Anesthesia</td>
			<td style="width:295px;">Torbugesic vet 10 mg/ml, Scanvet, Denmark</td>
			<td style="width:119px;"></td>
			<td>Alternative product may be used. Multiple suppliers</td>
		</tr>
		<tr height="20">
			<td height="20" style="height:20px;width:216px;">Neutral eye ointment</td>
			<td style="width:295px;"></td>
			<td style="width:119px;"></td>
			<td>Alternative product may be used. Multiple suppliers</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:216px;">Gauze or a cotton swab&#160;</td>
			<td style="width:295px;"></td>
			<td style="width:119px;"></td>
			<td>Alternative product may be used. Multiple suppliers</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:216px;">Disinfectant (70% alcohol)</td>
			<td style="width:295px;"></td>
			<td style="width:119px;"></td>
			<td>Alternative product may be used. Multiple suppliers</td>
		</tr>
	</tbody>
</table>

non-terminal blood sampling techniques in guinea pigs

خنازير غينيا تمتلك العديد من أوجه التشابه البيولوجية للإنسان ويتم التحقق من صحة النماذج الحيوانية التجريبية 1-3. ومع ذلك، فإن استخدام خنازير غينيا يمثل حاليا منطقة ضيقة نسبيا من البيانات البحثية وصفية حول منهجية محددة نادرة في المقابل. الميزات التشريحية للخنازير غينيا مختلفة قليلا عن نماذج القوارض الأخرى، وبالتالي تعديل تقنيات أخذ العينات لاستيعاب الاختلافات أنواع محددة، على سبيل المثال، مقارنة مع الفئران والجرذان، ضرورية للحصول على عينات كافية وعالية الجودة. على حد سواء طويلة وقصيرة الأجل في الدراسات المجراة في كثير من الأحيان تتطلب أخذ عينات الدم تتكرر اختيار تقنية ينبغي النظر جيدا من أجل الحد من التوتر وعدم الراحة في الحيوانات ولكن أيضا لضمان بقاء فضلا عن الامتثال مع متطلبات حجم العينة وسهولة الوصول إليها. ويمكن الحصول على عينات من الدم الوريدي في عدد من المواقع في خنازير غينيا على سبيل المثال.، والصافن والوريدالأوردة، كل تقنية تحتوي على كل مزايا وعيوب 4،5. هنا، نقدم أربع تقنيات مختلفة لأخذ عينات الدم إما واعية أو مخدرة خنازير غينيا. الإجراءات يتم توفير جميع الإجراءات غير الطرفية التي أحجام العينة وعدد العينات لا تتجاوز المبادئ التوجيهية لجمع الدم في الحيوانات المختبرية 6. تم اختبارها بدقة كل الأساليب المذكورة وتطبيقها لاخذ عينات من الدم المتكررة في الجسم الحي في الدراسات داخل منشأة أبحاثنا.

تم عرض أربعة أساليب مختلفة لغير الطرفية في الجسم الحي تقنيات أخذ العينات في الدم إما واعية أو مخدرة خنازير غينيا. ويوضح الشكل 1 مسار الجانبي الصافن والوريد الرصغي في خنزير غينيا ومواقع ثقب الممكنة. ويوضح الأوردة الأذن مرئية على السطح الظهري من الأذن خنز...

Watch this Scientific Journal Video about Non-Terminal Blood Sampling Techniques in Guinea Pigs at JoVE.com

Non-Terminal Blood Sampling Techniques in Guinea Pigs

على الرغم من نموذج معروف، خنزير غينيا يمثل حاليا مكانة في العلوم التجريبية والحيوان هو البيانات المحدود المتاح على تنفيذ معظم الإجراءات. هنا نقدم أربعة أساليب مختلفة لغير محطة في تقنيات أخذ العينات الدموية في الجسم الحي واعية إما مخدرة أو خنازير غينيا.

غير الطرفية تقنيات أخذ العينات الدم في غينيا الخنازير

Guinea pigs possess several biological similarities to humans and are validated experimental animal models1-3. However, the use of guinea pigs currently ...

non-terminal-blood-sampling-techniques-in-guinea-pigs

Research

JoVE Journal

Biology

37.1K Views.  University of Copenhagen.  على الرغم من نموذج معروف، خنزير غينيا يمثل حاليا مكانة في العلوم التجريبية والحيوان هو البيانات المحدود المتاح على تنفيذ معظم الإجراءات. هنا نقدم أربعة أساليب مختلفة لغير محطة في تقنيات أخذ العينات الدموية في الجسم الحي واعية إم...

Video: Non-Terminal Blood Sampling Techniques in Guinea Pigs

Optical Recording of Electrical Activity in Guinea-pig Enteric Networks using Voltage-sensitive Dyes

The enteric nervous system (ENS) is a self-contained network with identified functions, capable of performing complex behaviors in isolation. Its neurons (10 to 25 &mu;m in diameter) are arranged in plexuses that are confined to distinct planes of the gut wall 1; the myenteric plexus can be found between the longitudinal and circular muscle layers, and the submucous plexus between the circular muscle layer and the mucosa. Since the effector systems for these plexuses (transporting epithelium, endocrine cells, immune elements, blood vessels and smooth muscle) are also contained within the gut wall, semi-intact preparations can be dissected that preserve individual components of different reflex pathways. The behavior of the effector systems is controlled by the submucous and myenteric plexuses acting in concert. Therefore, detailed knowledge of synaptic interactions within and between ganglia, and of communication between the plexuses, is essential for understanding normal gastrointestinal function. The ENS, as an intact nervous system, is a unique experimental model in which one can correlate molecular and cellular events with the electrical behavior of the neuronal network and its physiological outputs. Because of the quasi-two-dimensional organization of its plexuses, the ENS is particularly well suited for the study of neural networks using multiple site optical recording techniques that employ voltage-sensitive dyes 2,7,8,9. We will illustrate here the use of a relatively new naphthylstyryl-pyridinium dye (di-4-ANEPPDHQ) 3 that offers multiple advantages over its predecessors, including very low phototoxicity, slow rate of internalization, and remarkable chemical stability. When used in conjunction with a camera that permits sub-millisecond time resolution, this dye allows us to monitor the electrical activity of all the neurons in the field of view with a maximal spatial resolution of ~ 2.5 &mu;m at 100X magnification. At lower magnification (10X or 20X), the sacrifice of single-cell resolution is compensated by a gain in perspective, revealing the intricacies of the inter-ganglionic circuitry.

This protocol illustrates how voltage-sensitive dyes enable optical recording of electrical activity from intact neural networks such as the plexuses of the guinea-pig enteric nervous system, with an adjustable resolution that ranges from single-cells to multi-ganglionic circuitry.

البصرية تسجيل النشاط الكهربائي في غينيا الخنازير المعوية باستخدام شبكات الجهد حساسة ملونات

The enteric nervous system (ENS) is a self-contained network with identified functions, capable of performing complex behaviors in isolation. Its neurons ...

Patch Clamp and Perfusion Techniques for Studying Ion Channels Expressed in Xenopus oocytes

The protocol presented here is designed to study the activation of the large conductance, voltage- and Ca2+-activated K+ (BK) channels. The protocol may also be used to study the structure-function relationship for other ion channels and neurotransmitter receptors1. BK channels are widely expressed in different tissues and have been implicated in many physiological functions, including regulation of smooth muscle contraction, frequency tuning of inner hair cells and regulation of neurotransmitter release2-6. BK channels are activated by membrane depolarization and by intracellular Ca2+ and Mg2+ 6-9. Therefore, the protocol is designed to control both the membrane voltage and the intracellular solution. In this protocol, messenger RNA of BK channels is injected into Xenopus laevis oocytes (stage V-VI) followed by 2-5 days of incubation at 18&deg;C10-13. Membrane patches that contain single or multiple BK channels are excised with the inside-out configuration using patch clamp techniques10-13. The intracellular side of the patch is perfused with desired solutions during recording so that the channel activation under different conditions can be examined. To summarize, the mRNA of BK channels is injected into Xenopus laevis oocytes to express channel proteins on the oocyte membrane; patch clamp techniques are used to record currents flowing through the channels under controlled voltage and intracellular solutions.

Patch Clamp and Perfusion Techniques for Studying Ion Channels Expressed in Xenopus oocytes

Ionic current of BK channels is recorded using patch clamp techniques. BK channels are expressed in Xenopus oocytes by injecting messenger RNA. The intracellular solution during patch clamp recordings is controlled by a perfusion system.

أعربت المشبك التصحيح وتقنيات الإرواء لدراسة في قنوات ايون القيطم البويضات

The protocol presented here is designed to study the activation of the large conductance, voltage- and Ca2+-activated K+ (BK) channels. The protocol may ...

Isolation and Culture of Pulmonary Endothelial Cells from Neonatal Mice

Endothelial cells provide a useful research model in many areas of vascular biology. Since its first isolation 1, human umbilical vein endothelial cells (HUVECs) have shown to be convenient, easy to obtain and culture, and thus are the most widely studied endothelial cells. However, for research focused on processes like angiogenesis, permeability or many others, microvascular endothelial cells (ECs) are a much more physiologically relevant model to study 2. Furthermore, ECs isolated from knockout mice provide a useful tool for analysis of protein function ex vivo. Several approaches to isolate and culture microvascular ECs of different origin have been reported to date 3-7, but consistent isolation and culture of pure ECs is still a major technical problem in many laboratories. Here, we provide a step-by-step protocol on a reliable and relatively simple method of isolating and culturing mouse lung endothelial cells (MLECs). In this approach, lung tissue obtained from 6- to 8-day old pups is first cut into pieces, digested with collagenase/dispase (C/D) solution and dispersed mechanically into single-cell suspension. MLECS are purified from cell suspension using positive selection with anti-PECAM-1 antibody conjugated to Dynabeads using a Magnetic Particle Concentrator (MPC). Such purified cells are cultured on gelatin-coated tissue culture (TC) dishes until they become confluent. At that point, cells are further purified using Dynabeads coupled to anti-ICAM-2 antibody. MLECs obtained with this protocol exhibit a cobblestone phenotype, as visualized by phase-contrast light microscopy, and their endothelial phenotype has been confirmed using FACS analysis with anti-VE-cadherin 8 and anti-VEGFR2 9 antibodies and immunofluorescent staining of VE-cadherin. In our hands, this two-step isolation procedure consistently and reliably yields a pure population of MLECs, which can be further cultured. This method will enable researchers to take advantage of the growing number of knockout and transgenic mice to directly correlate in vivo studies with results of in vitro experiments performed on isolated MLECs and thus help to reveal molecular mechanisms of vascular phenotypes observed in vivo.

Here, we describe a protocol for isolation and culture of murine pulmonary endothelial cells. This method comprises mechanic and enzymatic lung tissue dissociation as well as a 2-step purification process using anti-PECAM-1 and anti-ICAM-2 antibodies conjugated to magnetic beads, which produces a pure endothelial cell population of mostly microvascular origin.

العزلة والثقافة في الخلايا البطانية الرئوي من الفئران حديثي الولادة

Endothelial cells provide a useful research model in many areas of vascular biology. Since its first isolation 1, human umbilical vein endothelial cells ...

Techniques for the Analysis of Extracellular Vesicles Using Flow Cytometry

Extracellular Vesicles (EVs) are small, membrane-derived vesicles found in bodily fluids that are highly involved in cell-cell communication and help regulate a diverse range of biological processes. Analysis of EVs using flow cytometry (FCM) has been notoriously difficult due to their small size and lack of discrete populations positive for markers of interest. Methods for EV analysis, while considerably improved over the last decade, are still a work in progress. Unfortunately, there is no one-size-fits-all protocol, and several aspects must be considered when determining the most appropriate method to use. Presented here are several different techniques for processing EVs and two protocols for analyzing EVs using either individual detection or a bead-based approach. The methods described here will assist with eliminating the antibody aggregates commonly found in commercial preparations, increasing signal&#8211;to-noise ratio, and setting gates in a rational fashion that minimizes detection of background fluorescence. The first protocol uses an individual detection method that is especially well suited for analyzing a high volume of clinical samples, while the second protocol uses a bead-based approach to capture and detect smaller EVs and exosomes.

Many different methods exist for the measurement of extracellular vesicles (EVs) using flow cytometry (FCM). Several aspects should be considered when determining the most appropriate method to use. Two protocols for measuring EVs are presented, using either individual detection or a bead-based approach.

تقنيات لتحليل خارج الخلية الحويصلات عن طريق التدفق الخلوي

Extracellular Vesicles (EVs) are small, membrane-derived vesicles found in bodily fluids that are highly involved in cell-cell communication and help ...

Dried Blood Spots - Preparing and Processing for Use in Immunoassays and in Molecular Techniques

The idea of collecting blood on a paper card and subsequently using the dried blood spots (DBS) for diagnostic purposes originated a century ago. Since then, DBS testing for decades has remained predominantly focused on the diagnosis of infectious diseases especially in resource-limited settings or the systematic screening of newborns for inherited metabolic disorders and only recently have a variety of new and innovative DBS applications begun to emerge. For many years, pre-analytical variables were only inappropriately considered in the field of DBS testing and even today, with the exception of newborn screening, the entire pre-analytical phase, which comprises the preparation and processing of DBS for their final analysis has not been standardized. Given this background, a comprehensive step-by-step protocol, which covers al the essential phases, is proposed, i.e., collection of blood; preparation of blood spots; drying of blood spots; storage and transportation of DBS; elution of DBS, and finally analyses of DBS eluates. The effectiveness of this protocol was first evaluated with 1,762 coupled serum/DBS pairs for detecting markers of hepatitis B virus, hepatitis C virus, and human immunodeficiency virus infections on an automated analytical platform. In a second step, the protocol was utilized during a pilot study, which was conducted on active drug users in the German cities of Berlin and Essen.

The preparing and processing of dried blood spots (DBS) for their final analysis are still poorly standardized for most diagnostic applications. To overcome this shortcoming, a comprehensive step-by-step protocol is suggested and subsequently evaluated with regard to its effectiveness for detecting markers of viral infections.

بقع الدم المجفف-إعداد وتجهيز لاستخدامها في تحديدكم والتقنيات الجزيئية

The idea of collecting blood on a paper card and subsequently using the dried blood spots (DBS) for diagnostic purposes originated a century ago. Since ...

Sampling Blood from the Lateral Tail Vein of the Rat

Blood samples are commonly obtained in many experimental contexts to measure targets of interest, including hormones, immune factors, growth factors, proteins, and glucose, yet the composition of the blood is dynamically regulated and easily perturbed. One factor that can change the blood composition is the stress response triggered by the sampling procedure, which can contribute to variability in the measures of interest. Here we describe a procedure for blood sampling from the lateral tail vein in the rat. This procedure offers significant advantages over other more commonly used techniques. It permits rapid sampling with minimal pain or invasiveness, without anesthesia or analgesia. Additionally, it can be used to obtain large volume samples (upwards of 1 ml in some rats), and it may be used repeatedly across experimental days. By minimizing the stress response and pain resulting from blood sampling, measures can more accurately reflect the true basal state of the animal, with minimal influence from the sampling procedure itself.

Blood samples are useful for assessing biomarkers of physiological states or disease in vivo. Here we describe the methodology to sample blood from the lateral tail vein in the rat. This method provides rapid samples with minimal pain and invasiveness.

أخذ عينات الدم من الوريد الذيل الأفقي من الفئران

Blood samples are commonly obtained in many experimental contexts to measure targets of interest, including hormones, immune factors, growth factors, ...

Micron-scale Phenotyping Techniques of Maize Vascular Bundles Based on X-ray Microcomputed Tomography

It is necessary to accurately quantify the anatomical structures of maize materials based on high-throughput image analysis techniques. Here, we provide a 'sample preparation protocol' for maize materials (i.e., stem, leaf, and root) suitable for ordinary microcomputed tomography (micro-CT) scanning. Based on high-resolution CT images of maize stem, leaf, and root, we describe two protocols for the phenotypic analysis of vascular bundles: (1) based on the CT image of maize stem and leaf, we developed a specific image analysis pipeline to automatically extract 31 and 33 phenotypic traits of vascular bundles; (2) based on the CT image series of maize root, we set up an image processing scheme for the three-dimensional (3-D) segmentation of metaxylem vessels, and extracted two-dimensional (2-D) and 3-D phenotypic traits, such as volume, surface area of metaxylem vessels, etc. Compared with traditional manual measurement of vascular bundles of maize materials, the proposed protocols significantly improve the efficiency and accuracy of micron-scale phenotypic quantification.

We provide a novel method to improve the X-ray absorption contrast of maize tissue suitable for ordinary microcomputed tomography scanning. Based on CT images, we introduce a set of image-processing workflows for different maize materials to effectively extract microscopic phenotypes of vascular bundles of maize.

تقنيات Phenotyping ميكرون-مقياس الذرة حزم وعائية استناداً إلى التصوير المقطعي بالأشعة السينية ميكروكومبوتيد

It is necessary to accurately quantify the anatomical structures of maize materials based on high-throughput image analysis techniques. Here, we provide a ...

Gonadectomy and Blood Sampling Procedures in the Small Size Teleost Model Japanese Medaka (Oryzias latipes)

Sex steroids, produced by the gonads, play an essential role in brain and pituitary tissue plasticity and in the neuroendocrine control of reproduction in all vertebrates by providing feedback to the brain and pituitary. Teleost fishes possess a higher degree of tissue plasticity and variation in reproductive&#160;strategies compared to mammals and appear to be useful models to investigate the role of sex steroids and the mechanisms by which they act. The removal of the main source of sex steroid production using gonadectomy together with blood sampling to measure steroid levels has been well-established and fairly feasible in bigger fish and is a powerful technique to investigate the role and effects of sex steroids. However, these techniques raise challenges when implemented in small size teleost models. Here, we describe the step-by-step procedures of gonadectomy in both males and female Japanese medaka followed by blood sampling. These protocols are shown to be highly feasible in medaka indicated by a high survival rate, safety for the life span and phenotype of the fish, and reproducibility in terms of sex steroid clearance. The use of these procedures combined with the other advantages of using this small teleost model will greatly improve the understanding of feedback mechanisms in the neuroendocrine control of reproduction and tissue plasticity provided by sex steroids in vertebrates.

Gonadectomy and Blood Sampling Procedures in the Small Size Teleost Model Japanese Medaka Oryzias latipes

The article describes a quick protocol to gonadectomize and sample blood from the small teleost fish, using Japanese medaka (Oryzias latipes) as a model, to investigate the role of sex steroids in animal physiology.

إجراءات استئصال الغدد و أخذ عينات الدم في نموذج تيليوست صغير الحجم الياباني ميداكا (Oryzias latipes)

Sex steroids, produced by the gonads, play an essential role in brain and pituitary tissue plasticity and in the neuroendocrine control of reproduction in ...

Isolation of Retinal Pigment Epithelial Cells from Guinea Pig Eyes

This protocol describes the isolation of cells of the retinal pigment epithelium (RPE) from the eyes of young pigmented guinea pigs for potential application in molecular biology studies, including gene expression analyses. In the context of eye growth regulation and myopia, the RPE likely plays a role as a cellular relay for growth modulatory signals, as it is located between the retina and the two walls of the eye, such as the choroid and sclera. While protocols for isolating the RPE have been developed for both chicks and mice, these protocols have proven not to be directly translatable to the guinea pig, which has become an important and widely used mammalian myopia model. In this study, molecular biology tools were used to examine the expression of specific genes to confirm that the samples were free of contamination from the adjacent tissues. The value of this protocol has already been demonstrated in an RNA-Seq study of RPE from young pigmented guinea pigs exposed to myopia-inducing optical defocus. Beyond eye growth regulation, this protocol has other potential applications in studies of retinal diseases, including myopic maculopathy, one of the leading causes of blindness in myopes, in which the RPE has been implicated. The main advantage of this technique is that it is relatively simple and&#160;once perfected, yields high-quality RPE samples suitable for molecular biology studies, including RNA analysis.

We describe a simple and efficient method for isolating cells of the retinal pigment epithelium (RPE) cells from the eyes of young pigmented guinea pigs. This procedure allows for follow-up molecular biology studies on the isolated RPE, including gene expression analyses.

عزل الخلايا الظهارية الصبغية الشبكية من عيون خنزير غينيا

This protocol describes the isolation of cells of the retinal pigment epithelium (RPE) from the eyes of young pigmented guinea pigs for potential ...

Neutrophil Lifespan Extension with CLON-G and an In Vitro Spontaneous Death Assay

The average lifespan of a neutrophil is less than 24 h, which limits basic research on neutrophils and the application of neutrophil studies. Our previous research indicated that multiple pathways could mediate the spontaneous death of neutrophils. A cocktail was developed by simultaneously targeting these pathways, caspases-lysosomal membrane permeabilization-oxidant-necroptosis inhibition plus granulocyte colony-stimulating factor (CLON-G), which prolonged the neutrophil lifespan to greater than 5 days without significantly compromising the neutrophil function. Concurrently, a reliable and stable protocol for assessing and evaluating neutrophil death was also developed. In this work, we show that CLON-G can prolong the neutrophil lifespan in vitro to more than 5 days, and we exhibit the lengthening of the neutrophil lifespan with FACS and confocal fluorescence microscopy. This report introduces procedures for the preparation of CLON-G and showcases an in vitro spontaneous death assay of neutrophils, which can be used for the study of neutrophils and for subsequently interrogating neutrophil death, thus providing a reliable resource for the neutrophil community.

Neutrophil Lifespan Extension with CLON-G and an In Vitro Spontaneous Death Assay

This protocol details the preparation of CLON-G to extend the neutrophil lifespan to greater than 5 days and provides a reliable procedure for evaluating neutrophil death with flow cytometry and confocal fluorescence microscopy.

تمديد عمر العدلات مع CLON-G ومقايسة الموت التلقائي في المختبر

The average lifespan of a neutrophil is less than 24 h, which limits basic research on neutrophils and the application of neutrophil studies. Our previous ...