- activated ion currents triggered by ryanodine receptor - mediated 1 Ca 2 + release control the firing of inhibitory neurons in the prepositus

نویسندگان

  • Yasuhiko Saito
  • Yuchio Yanagawa
چکیده

35 Spontaneous miniature outward currents (SMOCs) are known to exist in smooth 36 muscles and peripheral neurons, and evidence for the presence of SMOCs in central 37 neurons has been accumulating. SMOCs in central neurons are induced through 38 Ca-activated K (KCa) channels, which are activated through Ca-induced Ca 39 release from the endoplasmic reticulum via ryanodine receptors (RyRs). Previously, 40 we found that some neurons in the prepositus hypoglossi nucleus (PHN) showed 41 spontaneous outward currents (SOCs). In the present study, we used whole-cell 42 recordings in slice preparations of the rat brainstem to investigate the following: 1) the 43 ionic mechanisms of SOCs, 2) the types of neurons exhibiting frequent SOCs, and 3) 44 the effect of Ca-activated conductance on neuronal firing. Pharmacological analyses 45 revealed that SOCs were induced via the activation of small conductance-type KCa 46 channels (SK channels) and RyRs, indicating that SOCs correspond to SMOCs. An 47 analysis of the voltage responses to current pulses of the fluorescence-expressing 48 inhibitory neurons of transgenic rats revealed that inhibitory neurons frequently 49 exhibited SOCs. The abolition of SOCs via the blockade of SK channels enhanced the 50 frequency of the spontaneous firing of inhibitory PHN neurons. However, the 51 abolition of SOCs via the blockade of RyRs reduced the firing frequency and 52

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Ca(2+)-activated ion currents triggered by ryanodine receptor-mediated Ca(2+) release control firing of inhibitory neurons in the prepositus hypoglossi nucleus.

Spontaneous miniature outward currents (SMOCs) are known to exist in smooth muscles and peripheral neurons, and evidence for the presence of SMOCs in central neurons has been accumulating. SMOCs in central neurons are induced through Ca(2+)-activated K(+) (K(Ca)) channels, which are activated through Ca(2+)-induced Ca(2+) release from the endoplasmic reticulum via ryanodine receptors (RyRs). Pr...

متن کامل

Spontaneous ryanodine-receptor-dependent Ca2+-activated K+ currents and hyperpolarizations in rat medial preoptic neurons.

The aim of the present study was to clarify the identity of slow spontaneous currents, the underlying mechanism and possible role for impulse generation in neurons of the rat medial preoptic nucleus (MPN). Acutely dissociated neurons were studied with the perforated patch-clamp technique. Spontaneous outward currents, at a frequency of approximately 0.5 Hz and with a decay time constant of appr...

متن کامل

Two intracellular pathways mediate metabotropic glutamate receptor-induced Ca2+ mobilization in dopamine neurons.

Activation of metabotropic glutamate receptors (mGluRs) causes membrane hyperpolarization in midbrain dopamine neurons. This hyperpolarization results from the opening of Ca(2+)-sensitive K(+) channels, which is mediated by the release of Ca(2+) from intracellular stores. Neurotransmitter-induced mobilization of Ca(2+) is generally ascribed to the action of inositol 1,4,5-triphosphate (IP(3)) i...

متن کامل

Group I mGluRs evoke K-ATP current by intracellular Ca2+ mobilization in rat subthalamus neurons.

We reported previously that Ca(2+) influx through N-methly-d-aspartate-gated channels evokes ATP-sensitive K(+) (K-ATP) currents in rat subthalamic nucleus (STN) neurons. By using whole-cell patch clamp recordings in brain slices, we investigated the ability of (RS)-3,5-dihydroxyphenylglycine (DHPG), a group I metabotropic glutamate receptor (mGluR) agonist, to evoke K-ATP currents. DHPG (20 µM...

متن کامل

Group I mGluRs Evoke K-ATP Current by Intracellular Ca Mobilization in Rat Subthalamus Neurons

We reported previously that Ca influx through N-methly-Daspartate-gated channels evokes ATP-sensitive K (K-ATP) currents in rat subthalamic nucleus (STN) neurons. By using whole-cell patch clamp recordings in brain slices, we investigated the ability of (RS)-3,5-dihydroxyphenylglycine (DHPG), a group I metabotropic glutamate receptor (mGluR) agonist, to evoke K-ATP currents. DHPG (20 mM) evoked...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:

دوره   شماره 

صفحات  -

تاریخ انتشار 2012