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Tytuł pozycji:

[Adult rat cardiomyocytes isolated by constant flow perfusion at low pressure].

Tytuł:
[Adult rat cardiomyocytes isolated by constant flow perfusion at low pressure].
Autorzy:
Wang YY; Department of Aerospace Physiology, Fourth Military Medical University, Xi'an 710032, China.
Zhang R
Yu ZB
Źródło:
Zhongguo ying yong sheng li xue za zhi = Zhongguo yingyong shenglixue zazhi = Chinese journal of applied physiology [Zhongguo Ying Yong Sheng Li Xue Za Zhi] 2005 Nov; Vol. 21 (4), pp. 475-9.
Typ publikacji:
English Abstract; Journal Article; Research Support, Non-U.S. Gov't
Język:
Chinese
Imprint Name(s):
Publication: Tianjin : Zhongguo ying yong sheng li xue za zhi bian ji bu
Original Publication: Beijing Shi : Zhongguo ying yong sheng li xue za zhi bian ji bu,
MeSH Terms:
Myocytes, Cardiac*
Cell Separation/*methods
Animals ; Perfusion ; Pressure ; Rats ; Rats, Sprague-Dawley
Entry Date(s):
Date Created: 20101225 Date Completed: 20120809 Latest Revision: 20101223
Update Code:
20240104
PMID:
21180180
Czasopismo naukowe
Aim: In order to get high-yield and high-quality cardiomyocytes from adult rat. We needed to clarify the optimal perfusion pressure in a constant flow condition and stopping digestion pressure.
Methods: The rat was injected with heparin (1 000 IU/kg, i. p.) 20 minutes prior to the experimental protocol. The heart was excised and the aorta was cannulated rapidly. The cannulated heart was mounted on a Langendorff perfusion apparatus with constant flow and perfusion pressure was monitored. The initial perfusion pressure was maintained at 15 kPa or 10 kPa by regulating the flow rate. The heart was digested by 0.08 % collagenase I at 37 degrees C and the enzymatic digestion was terminated immediately when the perfusion pressure was lowered to 10 kPa, 7.5 kPa or 5 kPa.
Results: While the initial perfusion pressure was 15 kPa (n = 4), enzymatic digestion induced great extent increment in perfusion pressure (maximal pressure > 25 kPa). The left ventricle was enlarged significantly and the contractility of myocytes was decreased. While the initial perfusion pressure was kept at 10 kPa, the digestion only resulted in less extent increment in perfusion pressure (maximal pressure < 18.75 kPa). The left ventricle was enlarged slightly. In the same initial perfusion pressure, if the digestion was stopped at 10 kPa (n = 3), or 5 kPa (n = 4), myocytes appeared over much or insufficiency digestion, respectively. The viability of freshly isolated cardiomyocytes was less than 10%. The most of myocytes died after restoration of extracellular Ca2+ concentration. If the digestion was stopped at 7.5 kPa (n = 15). The viability of cardiomyocytes was 82.6% +/- 4.8% in fresh isolation, 30.4% +/- 4.5% after restoration of normal extracellular Ca2+ concentration, or 24.8% +/- 5.4% after 4 h standing. The most of rod-shaped cardiomyocytes were quiescent and had visible cross striations, sharp edges, and normal contractility.
Conclusion: When the initial perfusion pressure is kept at 10 kPa (low pressure) and the enzymatic digestion is stopped at 7.5 kPa, high yield and high quality cardiomyocytes can be obtained.

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