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α-肾上腺素能对棕色脂肪细胞中⁸⁶Rb⁺(K⁺)电位和通量的影响。

Alpha-adrenergic effects on 86Rb+ (K+) potentials and fluxes in brown fat cells.

作者信息

Nånberg E, Nedergaard J, Cannon B

出版信息

Biochim Biophys Acta. 1984 Jul 20;804(3):291-300. doi: 10.1016/0167-4889(84)90132-0.

Abstract

Net K+ fluxes in isolated hamster brown fat cells were studied by the use of the K+ analogue 86Rb+. In isolated cells, cold-stored overnight to diminish K+ gradients, an equilibrium 86Rb+ (K+) clearance value of 27 microliter/million cells was obtained after 30 min incubation at 37 degrees C. This corresponds to a 10-fold K+ gradient over the plasma membrane, and a K+ potential of about -60 mV. The attainment of this equilibrium was dependent upon the presence of Na+ in the extracellular medium, and the uptake was fully inhibited by the (Na+ + K+)-ATPase inhibitor ouabain. Ouabain had, however, no significant acute effect on the maximal rate of thermogenesis achieved after norepinephrine stimulation of the cells, but if the restoration of ionic equilibrium was inhibited by ouabain in prolonged incubations, a decreased thermogenesis was observed. This was probably due to the low cytosolic K+ content then encountered, and the resulting inhibition of lipolysis. The addition of norepinephrine to cells in which 86Rb+ (K+) equilibrium had been attained resulted in a rapid efflux of 86Rb+ and the establishment of a new equilibrium value, at about 65% of the unstimulated value. This corresponds to a decrease in K+ potential of about 15 mV. The effect of norepinephrine was stereospecific and reversible, and had an EC50 value of about 10 nM. As catecholamine effects were much more sensitive to phentolamine than to propranolol, the adrenergically-induced efflux was classified as predominantly alpha-adrenergic. It is suggested that the norepinephrine-induced K+ efflux is due to a (probably Ca2+-mediated) opening of K+ channels in the cell membrane, and that this effect occurs secondarily to the alpha-adrenergically induced membrane depolarization (and increase in cytosolic Ca2+). The increased PK over the cell membrane would counteract further depolarization, and the K+ gradient would then approach the Nernst equilibrium under the new steady-state conditions.

摘要

利用钾离子类似物86Rb+对分离的仓鼠棕色脂肪细胞中的净钾离子通量进行了研究。在分离的细胞中,经过过夜冷藏以降低钾离子梯度,在37℃孵育30分钟后,获得了86Rb+(钾离子)清除率的平衡值为27微升/百万细胞。这相当于质膜上10倍的钾离子梯度,以及约 -60 mV的钾离子电位。该平衡的达到取决于细胞外介质中钠离子的存在,并且摄取被(钠 + 钾)-ATP酶抑制剂哇巴因完全抑制。然而,哇巴因对去甲肾上腺素刺激细胞后达到的最大产热速率没有显著的急性影响,但如果在长时间孵育中哇巴因抑制离子平衡的恢复,则观察到产热减少。这可能是由于当时遇到的胞质钾离子含量低,以及由此导致的脂解抑制。向已达到86Rb+(钾离子)平衡的细胞中添加去甲肾上腺素导致86Rb+快速外流,并建立了一个新的平衡值,约为未刺激值的65%。这相当于钾离子电位降低约15 mV。去甲肾上腺素的作用具有立体特异性且可逆,其EC50值约为10 nM。由于儿茶酚胺的作用对酚妥拉明比对普萘洛尔更敏感,因此肾上腺素能诱导的外流主要归类为α-肾上腺素能。有人提出,去甲肾上腺素诱导的钾离子外流是由于细胞膜中钾离子通道(可能由钙离子介导)的开放,并且这种作用继发于α-肾上腺素能诱导的膜去极化(以及胞质钙离子增加)。细胞膜上增加的钾离子通透性将抵消进一步的去极化,然后钾离子梯度将在新的稳态条件下接近能斯特平衡。

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