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1
Negative feed-back regulation of noradrenaline release by nerve stimulation in the perfused cat's spleen: differences in potency of phenoxybenzamine in blocking the pre- and post-synaptic adrenergic receptors.灌注猫脾脏中神经刺激对去甲肾上腺素释放的负反馈调节:酚苄明阻断突触前和突触后肾上腺素能受体的效力差异。
J Physiol. 1974 Mar;237(3):505-19. doi: 10.1113/jphysiol.1974.sp010495.
2
Nerve stimulation-meditated overflow of norepinephrine and dopamine-beta-hydroxylase. III. Effects of norepinephrine depletion on the alpha presynaptic regulation of release.神经刺激介导的去甲肾上腺素和多巴胺-β-羟化酶的溢出。III. 去甲肾上腺素耗竭对释放的α突触前调节的影响。
J Pharmacol Exp Ther. 1975 Jan;192(1):1-14.
3
Influence of reserpine-induced depletion of noradrenaline on the negative feed-back mechanism for transmitter release during nerve stimulation.利血平诱导的去甲肾上腺素耗竭对神经刺激期间递质释放的负反馈机制的影响。
Br J Pharmacol. 1973 Oct;49(2):214-25. doi: 10.1111/j.1476-5381.1973.tb08367.x.
4
Protection by phentolamine against the effects of phenoxybenzamine on transmitter release elicited by nerve stimulation in the perfused cat heart.酚妥拉明对酚苄明在灌注猫心脏中神经刺激引发的递质释放效应的保护作用。
Br J Pharmacol. 1974 Dec;52(4):549-57. doi: 10.1111/j.1476-5381.1974.tb09723.x.
5
Evidence against a physiological role of prostaglandins in the regulation of noradrenaline release in the cat spleen.关于前列腺素在猫脾脏去甲肾上腺素释放调节中生理作用的反对证据。
J Physiol. 1975 Oct;251(3):737-62. doi: 10.1113/jphysiol.1975.sp011119.
6
Role of the -adrenoceptor in regulating noradrenaline overflow by nerve stimulation.β-肾上腺素能受体在通过神经刺激调节去甲肾上腺素溢出中的作用。
Br J Pharmacol. 1972 Apr;44(4):672-88. doi: 10.1111/j.1476-5381.1972.tb07306.x.
7
Vascular responses and noradrenaline overflows in the isolated blood-perfused cat spleen: some effects of cocaine, normetanephrine and -blocking agents.离体血液灌注猫脾脏中的血管反应和去甲肾上腺素外溢:可卡因、去甲变肾上腺素和β受体阻断剂的某些作用
J Physiol. 1972 Dec;227(3):647-64. doi: 10.1113/jphysiol.1972.sp010052.
8
The effects of labetalol (AH 5158) on adrenergic transmission in the cat spleen.拉贝洛尔(AH 5158)对猫脾脏肾上腺素能传递的影响。
Br J Pharmacol. 1977 Apr;59(4):643-50. doi: 10.1111/j.1476-5381.1977.tb07733.x.
9
Inhibition by dopamine of 3H-noradrenaline release elicited by nerve stimulation in the isolated cat's nictitating membrane.多巴胺对猫离体瞬膜神经刺激诱发的3H-去甲肾上腺素释放的抑制作用。
Naunyn Schmiedebergs Arch Pharmacol. 1975;289(2):179-203. doi: 10.1007/BF00501305.
10
Influence of the frequency of nerve stimulation on the metabolism of 3H-norepinephrine released from the perfused cat spleen: differences observed during and after the period of stimulation.神经刺激频率对灌注猫脾脏释放的3H-去甲肾上腺素代谢的影响:刺激期间及刺激后观察到的差异。
J Pharmacol Exp Ther. 1976 Jul;198(1):83-101.

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The expanding roles and mechanisms of G protein-mediated presynaptic inhibition.G 蛋白介导电突触前抑制的作用不断扩大及其机制。
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Clin Auton Res. 1999 Jun;9(3):145-59. doi: 10.1007/BF02281628.
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Involvement of pertussis toxin-sensitive and -insensitive mechanisms in alpha-adrenoceptor modulation of noradrenaline release from rat sympathetic neurones in tissue culture.百日咳毒素敏感和不敏感机制在组织培养中对大鼠交感神经元去甲肾上腺素释放的α-肾上腺素能受体调节中的作用。
Br J Pharmacol. 1993 Sep;110(1):281-8. doi: 10.1111/j.1476-5381.1993.tb13806.x.
6
Effects of human recombinant interleukins on stimulation-evoked noradrenaline overflow from the rat perfused spleen.人重组白细胞介素对大鼠离体灌注脾脏刺激诱发去甲肾上腺素溢出的影响。
Naunyn Schmiedebergs Arch Pharmacol. 1994 May;349(5):497-502. doi: 10.1007/BF00169139.
7
The role of presynaptic receptors in the cardiovascular actions of N,N-di-n-propyldopamine in the cat and dog.突触前受体在猫和犬体内N,N-二正丙基多巴胺心血管作用中的角色。
Naunyn Schmiedebergs Arch Pharmacol. 1980 Oct;314(1):17-28. doi: 10.1007/BF00498427.
8
Cardiovascular effects of intracerebroventricular GABA, glycine and muscimol in the rat.大鼠脑室内注射γ-氨基丁酸、甘氨酸和蝇蕈醇对心血管系统的影响。
Naunyn Schmiedebergs Arch Pharmacol. 1980 Sep;313(3):225-36. doi: 10.1007/BF00505738.
9
Involvement of catecholamines in acute tolerance to ethanol in mice.儿茶酚胺在小鼠乙醇急性耐受性中的作用。
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10
Characterization of alpha adrenoceptors in pial arteries of the bovine brain.牛脑软脑膜动脉中α肾上腺素能受体的特性研究
Naunyn Schmiedebergs Arch Pharmacol. 1983 Sep;324(2):88-93. doi: 10.1007/BF00497012.

本文引用的文献

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[EFFECTS OF PHENOXYBENZAMINE, PHENTOLAMINE AND AZAPETINE ON ADRENERGIC SYNAPSES OF THE CAT SPLEEN. BLOCKADE OF ALPHA-ADRENERGIC RECEPTORS AND INHIBITION OF RE-UPTAKE OF NEURALLY RELEASED NORADRENALINE].[苯氧苄胺、酚妥拉明和阿扎培丁对猫脾脏肾上腺素能突触的作用。α-肾上腺素能受体的阻断及对神经释放去甲肾上腺素再摄取的抑制]
Helv Physiol Pharmacol Acta. 1964;22:148-61.
2
REMOVAL OF INFUSED NOREPINEPHRINE BY THE CAT'S SPLEEN; MECHANISM OF ITS INHIBITION BY PHENOXYBENZAMINE.猫脾脏对注入去甲肾上腺素的清除作用;苯氧苄胺对其抑制的机制。
Experientia. 1963 Nov 15;19:601-2. doi: 10.1007/BF02151014.
3
The effect of neuronal rest on the output of sympathetic transmitter from the spleen.神经元静息对脾脏交感递质输出的影响。
J Physiol. 1961 Dec;159(2):365-80. doi: 10.1113/jphysiol.1961.sp006814.
4
The output of sympathetic transmitter from the spleen of the cat.猫脾脏交感递质的释放
J Physiol. 1957 Aug 29;138(1):81-102. doi: 10.1113/jphysiol.1957.sp005839.
5
Evidence that blockade of adrenergic receptors causes overflow of norepinephrine in cats colon after nerve stimulation.有证据表明,在猫结肠神经受到刺激后,肾上腺素能受体的阻断会导致去甲肾上腺素外溢。
J Pharmacol Exp Ther. 1967 Jul;157(1):125-34.
6
The uptake and release of radioactive noradrenaline by the splenic nerves of cats.猫脾神经对放射性去甲肾上腺素的摄取与释放
J Physiol. 1966 Nov;187(1):51-68. doi: 10.1113/jphysiol.1966.sp008075.
7
Apparent depletion of NE stores after repetitive stimulation of cat colon in presence of phenoxybenzamine.在苯氧苄胺存在的情况下,重复刺激猫结肠后去甲肾上腺素储备的明显耗竭。
Int J Neuropharmacol. 1966 Jul;5(4):293-8. doi: 10.1016/0028-3908(66)90037-2.
8
Relation between the rate of stimulation and the quantity of noradrenaline liberated from sympathetic nerve endings in the isolated perfused spleen of the cat.猫离体灌注脾脏中刺激速率与交感神经末梢释放去甲肾上腺素量之间的关系。
J Physiol. 1965 Nov;181(1):48-58. doi: 10.1113/jphysiol.1965.sp007744.
9
Dual site of action of phenoxybenzamine in the cat's spleen; blockade of alpha-adrenergic receptors and inhibition of re-uptake of neurally released norepinephrine.酚苄明在猫脾脏中的双重作用位点;α-肾上腺素能受体阻断和对神经释放去甲肾上腺素再摄取的抑制。
Experientia. 1964 May 15;20(5):272-3. doi: 10.1007/BF02151802.
10
Decrease in effectiveness of phenoxybenzamine after chronic denervation and chronic decentralization of the nictitating membrane of the pithed cat.去脑猫瞬膜慢性去神经支配和慢性去中枢支配后苯氧苄胺效能的降低
J Pharmacol Exp Ther. 1968 Oct;163(2):290-9.

灌注猫脾脏中神经刺激对去甲肾上腺素释放的负反馈调节:酚苄明阻断突触前和突触后肾上腺素能受体的效力差异。

Negative feed-back regulation of noradrenaline release by nerve stimulation in the perfused cat's spleen: differences in potency of phenoxybenzamine in blocking the pre- and post-synaptic adrenergic receptors.

作者信息

Dubocovich M L, Langer S Z

出版信息

J Physiol. 1974 Mar;237(3):505-19. doi: 10.1113/jphysiol.1974.sp010495.

DOI:10.1113/jphysiol.1974.sp010495
PMID:4363457
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1350902/
Abstract
  1. The effects of low concentrations of phenoxybenzamine (8.8 x 10(-10) to 2.9 x 10(-7)M) on responses and on noradrenaline overflow elicited by nerve stimulation were studied in the perfused cat's spleen.2. In the presence of 8.8 x 10(-10)M or 2.9 x 10(-9)M phenoxybenzamine there was a significant reduction in responses to nerve stimulation while the overflow of the transmitter did not increase at the two frequencies of stimulation employed: 5 and 30 Hz.3. In the presence of 2.9 x 10(-8)M or 2.9 x 10(-7)M phenoxybenzamine the responses to nerve stimulation were practically abolished and a significant increase in transmitter overflow was obtained at both frequencies of stimulation. The drug was more effective in increasing transmitter overflow at 5 Hz when compared with 30 Hz.4. The higher effectiveness of phenoxybenzamine in blocking the post-synaptic alpha-receptor when compared with the blockade of the presynaptic alpha-receptor that regulates transmitter release is compatible with the view that these two receptors are not identical.5. A second alternative for the difference in effectiveness of phenoxybenzamine is that both types of alpha receptors are identical, but the spare receptor capacity for the presynaptic adrenergic receptors is higher than that of the post-synaptic receptors.
摘要
  1. 研究了低浓度苯氧苄胺(8.8×10⁻¹⁰至2.9×10⁻⁷M)对灌注猫脾脏中神经刺激引发的反应及去甲肾上腺素溢出的影响。

  2. 在存在8.8×10⁻¹⁰M或2.9×10⁻⁹M苯氧苄胺的情况下,对神经刺激的反应显著降低,而在所采用的两个刺激频率(5Hz和30Hz)下,递质溢出并未增加。

  3. 在存在2.9×10⁻⁸M或2.9×10⁻⁷M苯氧苄胺的情况下,对神经刺激的反应几乎完全消失,且在两个刺激频率下均观察到递质溢出显著增加。与30Hz相比,该药物在5Hz时增加递质溢出的效果更明显。

  4. 与调节递质释放的突触前α受体阻断相比,苯氧苄胺对突触后α受体的阻断效果更强,这与这两种受体并不相同的观点相符。

  5. 苯氧苄胺有效性差异的另一种解释是,两种类型的α受体是相同的,但突触前肾上腺素能受体的备用受体容量高于突触后受体。