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冷冻保存后人肺动脉功能活性的维持

Maintenance of functional activity of human pulmonary arteries after cryopreservation.

作者信息

Ellis P, Müller-Schweinitzer E

机构信息

Sandoz Pharma AG, Basel, Switzerland.

出版信息

Br J Pharmacol. 1991 Jun;103(2):1377-80. doi: 10.1111/j.1476-5381.1991.tb09797.x.

Abstract
  1. Human intrapulmonary arteries have been investigated in vitro in fresh tissue or after storage at -190 degrees C in foetal calf serum containing 1.8 M dimethyl sulphoxide. 2. After cryopreservation of the arteries, maximal contractile force was reduced to 76%. This was assessed by the responses (in g) to 10 nM of the thromboxane analogue, U 46619. 3. Constricting agonists such as noradrenaline, 5-hydroxytryptamine, histamine and U 46619 stimulated fresh and frozen/thawed arteries producing pD2 values similar to the respective values determined on fresh tissues. 4. Endothelium-independent relaxant responses of U 46619-precontracted arteries to prostacyclin (PGI2), aminophylline and papaverine were generally unchanged after storage. The same was true for relaxant response to the potassium channel activator P-1075 whereas the pD2 values for SDZ PCO 400, RP 49356 and cromakalim were somewhat diminished. 5. Nevertheless, a significant correlation was obtained when the apparent pD2 values for all agonists on fresh and frozen/thawed tissues were compared (P less than 0.001). 6. The evidence suggests that after cryopreservation of human intrapulmonary arteries at -190 degrees C, mechanisms of both contraction and relaxation are well-maintained.
摘要
  1. 已在新鲜组织中或在含有1.8M二甲基亚砜的胎牛血清中于-190℃储存后,对人肺内动脉进行了体外研究。2. 动脉冷冻保存后,最大收缩力降低至76%。这是通过对10nM血栓素类似物U 46619的反应(以克为单位)来评估的。3. 诸如去甲肾上腺素、5-羟色胺、组胺和U 46619等收缩激动剂刺激新鲜的和冷冻/解冻的动脉,产生的pD2值与在新鲜组织上测定的相应值相似。4. U 46619预收缩的动脉对前列环素(PGI2)、氨茶碱和罂粟碱的内皮依赖性舒张反应在储存后通常未改变。对钾通道激活剂P-1075的舒张反应也是如此,而SDZ PCO 400、RP 49356和克罗卡林的pD2值有所降低。5. 然而,当比较新鲜组织和冷冻/解冻组织上所有激动剂的表观pD2值时,得到了显著的相关性(P小于0.001)。6. 证据表明,在-190℃对人肺内动脉进行冷冻保存后,收缩和舒张机制均得到良好维持。

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本文引用的文献

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Endothelium-dependent relaxation of human pulmonary arteries.人肺动脉的内皮依赖性舒张
Am J Physiol. 1987 Feb;252(2 Pt 2):H434-8. doi: 10.1152/ajpheart.1987.252.2.H434.

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