Saeko Sakai
Tokyo Medical University
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Featured researches published by Saeko Sakai.
Neurourology and Urodynamics | 2009
Toshihide Shishido; Saeko Sakai; Tsuneo Tosaka
The importance of the T‐ and L‐type Ca2+ channels on the α1‐adrenoceptor‐mediated contraction of guinea‐pig vas deferens was investigated in relation to the SK and BK channels.
Neurochemical Research | 1989
Junko Tasaka; Saeko Sakai; Tsuneo Tosaka; Isao Yoshihama
The kinetics and specificity of GABA and taurine uptake were studied in the bullfrog sympathetic ganglia. GABA uptake system consisted of simple saturable component and taurine uptake system consisted of two saturable components exclusive of non-saturable influx. Taurine unaffected GABA uptake while GABA inhibited taurine uptake competitively with theKi/Km ratio of 38. GABA (5.14 μM) uptake was inhibited by δ-aminovaleric acid and slightly by 2,4-diaminobutyric acid (5 mM, each) among ten structural analogs. Taurine uptake under high-affinity conditions was most strongly suppressed by hypotaurine and β-alanine competitively with theKi/Km ratio of 1.0 and 1.9, respectively. Autoradiography showed that glial cells were heavily labeled by both [3H]GABA and [3H]taurine. These results suggest that GABA is transported by a highly specific carrier system distinct from the taurine carrier and that taurine, hypotaurine, and β-alanine may share the same high-affinity carrier system in the glial cells of the bullfrog sympathetic ganglia.
Neurochemical Research | 1990
Saeko Sakai; Junko Tasaka; Tsuneo Tosaka
The kinetics of sodium dependency of GABA uptake by satellite glial cells was studied in bullfrog sympathetic ganglia. GABA uptake followed simple Michaelis-Menten kinetics at all sodium concentrations tested. Increasing external sodium concentration increased bothKm andVmax for GABA uptake, with an increase in theVmax/Km ratio. The initial rate of uptake as a function of the sodium concentration exhibited sigmoid shape at 100 μM GABA. Hill number was estimated to be 2.0. Removal of external potassium ion or 10 μM ouabain reduced GABA uptake time-dependently. The effect of ouabain was potentiated by 100 μM veratrine. These results suggest that at least two sodium ions are involved with the transport of one GABA molecule and that sodium concentration gradient across the plasma membrane is the main driving force for the transport of GABA. The essential sodium gradient may be maintained by Na+, K+-ATPase acting as an ion pump.
Neuroscience Research | 1998
Saeko Sakai; Tsuneo Tosaka
554 ABNORMAL NEURAL INPUTS FROM THE MEDIAN PREOPTIC NUCLEUS TO THE HYPOTHALAMIC PARAVENTJUCULAR NUCLEUS IN SPONTANEOUSLY HYPERTENSIVE RATS JUNICHI TANAKA’, YASUSHI HAYASHI 2, KATSUHIDE KARIYA3, MASAHIKO NOMURA4 Depts. of ‘Human Dev. and 2Educ. for Handicapped Child., Naruto Univ. of Educ., Naruto, Tokushima 772-8502, 3Res. Lab., Torii & Co. Ltd., Midori-ku, Chiba 267-0056, 4Dept. of Physiol., Saitama Med. Sch., lruma-gun, Saitama, 350-0495 Extracellular single-unit activity was recorded from phasically firmg neurohypophyseal neurons tn the hypothalamic paraventricularnucleus (PVN) of male Wistar-Kyoto (WKY, 40 units) and spontaneously hypertensive rats (SHR, 38 units) under urethane anesthesia. Electrical stimulation of the median preoptic nucleus (MnPO) J)roduced orthodromic excitatton (48% in WKY rats; 51% in SHR) or inhibition (10% in WKY rats; 13% in SHR) of the activity of PVN units. No signifmant differences in the latency, duration or threshold of the MnPG stimulus-induced responses were observed between WKY and SHR. The magnitude of excitatory response, but not the inhtbitory response, much greater in SHR than m WKY rats. Local administration of angiotensin II (ANG II) into the stimulation sites enhanced the neuronal activity of units (64% in WKY rats; 67% in SHR) that displayed the excitation to electrical stimulation of the MnPO. The duration and frequency of excitatory response caused by the ANG II injection was much greater in SHR than in WKY rats. These results suggest that ANG IIsensitive MnPO efferents to the PVN act to facilitate the excitability of putative vasopressin-secreting neurons in the PVN and imply that there is the alteration between WKY and SHR in the functron of the pathways.
Neuroscience Research | 1997
Saeko Sakai; Isao Yoshihama; Fumihiko Hokoishi; Kazunori Namiki; Masashi Ogawa; Makoto Miki; Tsuneo Tosaka
SAEKO SAKAI’ , ISA0 YOSHIHAMA3. FCSIIHIKO HOKOISHI’. KXZUNORI NAMIKI’. 5IASASHI OGAWA2, MAKOTO MIK12, TSUNEO TOSAKA’ The thermal effects on contraction, binding kinetics of [3H]prazosin and histology were examined in the guineapig vas deferens. The contraction was recorded at 36°C after thermal exposure to 43-47°C for 1 h. The binding kinetics of cri-adrenoceptors was determined at 43-55°C. No significant changes in the contraction and the kinetic parameters were observed at 43°C. The contractions induced by phenylephrine. .ATP. ?L1Ch, nicotine. KC1 and electrical stimulation were abolished at 47°C. whereas the number of binding sites reduced by 54% at 55°C. Serious damage of the muscle fibers was observed at 50°C. Autoradiography of tritiated or. a2 and P-antagonists revealed that the muscle membrane was predominantly labeled with silver grains. The results indicate that the nerve fibers and the contractile elements were intact at 43”C, and that the muscle fibers lost their contractility at 47°C; although al-adrenoceptors tolerated against much higher thermal stress.
The Japanese Journal of Urology | 1998
Masashi Ogawa; Kazunori Namiki; Makoto Miki; Saeko Sakai; Isao Yoshihama
The Japanese Journal of Urology | 2000
Toshihide Shishido; Kazunori Namiki; Makoto Miki; Saeko Sakai; Tsuneo Tosaka
Neuroscience Research Supplements | 1992
Saeko Sakai; Tsuneo Tosaka
Neuroscience Research Supplements | 1991
Saeko Sakai; Junko Tasaka; Tsuneo Tosaka
Neuroscience Research Supplements | 1991
Takefumi Miyazaki; Junko Tasaka; Saeko Sakai; Toshio Hashiguchi; Tsuneo Tosaka