Kachadorian W A, Muller J
J Membr Biol. 1984;77(2):161-7. doi: 10.1007/BF01925864.
We studied the effects of potassium-free media on processes related to the hydro-osmotic response of toad bladder to ADH (20 mU/ml). Exposure of bladders to potassium-free media did not affect base-line osmotic water flow, but it promptly attenuated the level of osmotic water permeability induced by ADH. Both the frequency of hormonally induced intra(luminal)membrane particle aggregates (presumed sites for transmembrane water flow) and the number of luminal membrane fusion events (associated with aggregate delivery from the cytoplasm) were also reduced. Potassium-free media had no measurable effect either on cytoplasmic microtubule integrity or on mean aggregate size. Potassium repletion reversed the inhibitory effect of potassium-free media on ADH-related osmotic water permeability. For bladders fully stimulated with ADH in the presence of potassium, subsequent bathing media depletion of potassium led to an inhibition of ADH-related water flow and to reductions in membrane fusion sites and aggregates. We confirmed that the inhibitory effect of potassium-free media on ADH-induced osmotic water permeability results from serosal bathing medium potassium depletion alone and occurs at a post-cyclic AMP site. In addition, we found that ADH-stimulated water permeability was attenuated in bathing media containing a low potassium concentration (0.5 mM). The data are consistent with the view that potassium-free media or media containing low levels of potassium inhibit ADH-enhanced osmotic water permeability in toad bladder by interfering with the process of or leading to membrane fusion required for the delivery of water-conducting structures to the luminal membrane. In addition, some of our results imply that aggregates may turn over during sustained ADH stimulation.
我们研究了无钾培养基对蟾蜍膀胱对抗利尿激素(20 mU/ml)的水渗透反应相关过程的影响。将膀胱暴露于无钾培养基中不会影响基线渗透水流,但会迅速减弱抗利尿激素诱导的渗透水通透性水平。激素诱导的(管腔内)膜颗粒聚集体(推测为跨膜水流的位点)的频率以及管腔膜融合事件的数量(与从细胞质递送聚集体相关)也都减少了。无钾培养基对细胞质微管完整性或平均聚集体大小均无显著影响。补充钾可逆转无钾培养基对与抗利尿激素相关的渗透水通透性的抑制作用。对于在有钾存在的情况下用抗利尿激素充分刺激的膀胱,随后将培养基中的钾耗尽会导致与抗利尿激素相关的水流受到抑制,以及膜融合位点和聚集体减少。我们证实,无钾培养基对抗利尿激素诱导的渗透水通透性的抑制作用仅源于浆膜浴培养基中钾的耗尽,且发生在环磷酸腺苷作用位点之后。此外,我们发现,在含有低钾浓度(0.5 mM)的浴培养基中,抗利尿激素刺激的水通透性会减弱。这些数据与以下观点一致:无钾培养基或低钾培养基通过干扰将水传导结构递送至管腔膜所需的膜融合过程或导致该过程发生,从而抑制蟾蜍膀胱中抗利尿激素增强的渗透水通透性。此外,我们的一些结果表明,在持续的抗利尿激素刺激过程中,聚集体可能会更新。