Muñoz D J, Thorne P R, Housley G D, Billett T E, Battersby J M
Department of Physiology, University of Auckland, New Zealand.
Hear Res. 1995 Oct;90(1-2):106-118. doi: 10.1016/0378-5955(95)00152-3.
There is strong evidence for the presence of P2 purinoceptors on cochlear tissues, but the role of extracellular ATP in cochlear function is still unclear. Our previous studies have determined the presence of ATP in the cochlear fluids and indicated that the purinoceptors are substantially localized to the tissues lining the endolymphatic compartment. This implies that extracellular ATP may have an humoral role confined to the endolymphatic space. In order to study the influence of extracellular ATP in the endolymphatic space, a series of studies were undertaken in which ATP (10 microM to 10 mM) in artificial endolymph (EL) (test solution: 2-12.5 nl) was injected into the scala media and the effect on the cochlear microphonic (CM) and endocochlear potential (EP) evaluated. A double-barrelled pipette, with one barrel containing the test solution and the other artificial EL (control solution) was inserted into scala media of the third turn of the guinea-pig cochlea. A known volume (2-12.5 nl) of test or control solution was then pressure-injected into the space. ATP had a significant dose-dependent suppressive effect on both EP and CM with a threshold of approximately 2 x 10(-14) mol; the response was readily reversible, also in a dose-dependent fashion. Artificial EL of the same volume had no effect on EP and CM. The ATP effect on EP was blocked by the P2 purinoceptor antagonists suramin and reactive blue 2 (RB2). Neither adenosine (2 x 10(-13) to 2 x 10(-11) mol) nor suramin or RB2 on their own had any effect on EP and CM. This study provides the first evidence for an effect of extracellular ATP in the endolymphatic compartment on cochlear function which is mediated via P2 purinoceptors. This provides supporting evidence for an humoral role for extracellular ATP in the modulation of cochlear function.
有充分证据表明耳蜗组织上存在P2嘌呤受体,但细胞外ATP在耳蜗功能中的作用仍不清楚。我们之前的研究已确定耳蜗液中存在ATP,并表明嘌呤受体主要定位于内淋巴腔室的衬里组织。这意味着细胞外ATP可能具有局限于内淋巴空间的体液作用。为了研究细胞外ATP在内淋巴空间中的影响,我们进行了一系列研究,将人工内淋巴(EL)(测试溶液:2 - 12.5 nl)中的ATP(10 microM至10 mM)注入中阶,并评估其对耳蜗微音器电位(CM)和内耳蜗电位(EP)的影响。将一个双管移液器插入豚鼠耳蜗第三圈的中阶,其中一个管中装有测试溶液,另一个管中装有人工EL(对照溶液)。然后将已知体积(2 - 12.5 nl)的测试或对照溶液压力注入该空间。ATP对EP和CM均有显著的剂量依赖性抑制作用,阈值约为2×10^(-14) mol;该反应也很容易以剂量依赖的方式逆转。相同体积的人工EL对EP和CM没有影响。ATP对EP的作用被P2嘌呤受体拮抗剂苏拉明和反应性蓝2(RB2)阻断。单独的腺苷(2×10^(-13)至2×10^(-11) mol)、苏拉明或RB2对EP和CM均无任何影响。本研究首次证明内淋巴腔室中的细胞外ATP通过P2嘌呤受体介导对耳蜗功能产生影响。这为细胞外ATP在调节耳蜗功能中的体液作用提供了支持性证据。