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1 cose and lactate, respectively, in rat brain microdialysate.
2 gin of neurochemicals in cerebrospinal fluid microdialysate.
3 determine the glutamate concentration in the microdialysate.
4 panel of monoamines in rat prefrontal cortex microdialysates.
5 as not applicable to the high ionic strength microdialysates.
6 inistered directly into the striatum via the microdialysate (20 microM of METH for 10 min), or via pe
7 and males showed nearly a 4-fold increase in microdialysate 5-HT in response to fluoxetine while smal
8 terone, 48 h after estrogen priming, reduced microdialysate 5-HT near the threshold for detection.
9 pike analyses of offline-collected rat brain microdialysate and (ii) in vivo dynamic monitoring of th
10 n hypothalamic paraventricular nucleus (PVN) microdialysate and arterial plasma simultaneously during
11 etermine the degree of equilibration between microdialysate and interstitium for each probe to accura
12 ne and large neutral amino acids in striatal microdialysate, as well as in tissue from striatum and m
13           Proestrous females had the highest microdialysate concentrations of 5-HT during the light p
14 hepin, a 5-HT receptor antagonist, increased microdialysate concentrations of 5-HT.
15                                       Often, microdialysate concentrations of an analyte are only a f
16                                 At baseline, microdialysate contained low levels of IL-1alpha, IL-5,
17 is study, polygraphic recordings and caudate microdialysate dopamine measurements in narcoleptic dogs
18 nthesis and examined DOPA levels in striatal microdialysate during perfusion with NSD-1015.
19                                     Striatal microdialysates, each collected over a 20 min interval,
20 high-velocity impact traumatic brain injury, microdialysate extracellular fluid neurofilament heavy c
21                   At rest, blood samples and microdialysates from adipose tissue and skeletal muscle
22 of ascorbic-acid and antioxidant capacity in microdialysates from cladodes of Opuntia ficus-indica (L
23  pyruvate metabolic process were elevated in microdialysates from lesional AD skin compared with both
24                                  In striatal microdialysate, GBL markedly lowered DA levels; tyrosine
25 er plasma glucose was associated with higher microdialysate glucose.
26 1 excretion, renal cortical ET-1 addition to microdialysate in vivo, and renal cortical ET-1 mRNA, co
27 nalytical chemical measurements of intra-SCN microdialysates in mouse, we found significant neurotran
28 g/kg i.p.) increased DOPA levels in striatal microdialysate, increased tissue DA levels in the MPFC a
29                By sequentially loading brain microdialysate into the dual sample collection loops, th
30                                   2.5 muL of microdialysate is obtained and analyzed for inorganic ca
31 5-HT), and normetanephrine (NM) in rat brain microdialysates is to improve detection sensitivity.
32                                              Microdialysate lactate and pyruvate were unchanged, but
33                                    IL and IP microdialysate lactate, pyruvate, glucose and glycerol w
34 his method, 3-NT was detected in human liver microdialysate (levels up to 2.6 nM), although levels in
35 f intraperitoneal (IP) and intraluminal (IL) microdialysate metabolites in depicting ex vivo small in
36                    Ex vivo time sequences of microdialysate metabolites were described and ROC analys
37 ytes at baseline and only slightly augmented microdialysate NE responses to IMMO.
38 induced prolonged elevations of hypothalamic microdialysate NE, as well as plasma ACTH and corticoste
39 s by 4.3, 7.3, 2.5, 0.6 and 1.8-fold and PVN microdialysate NE, DHPG, and DOPAC by 1.2, 0.6 and 0.5-f
40  also enhanced effects of IMMO on plasma and microdialysate NE, DHPG, and DOPAC.
41 table in suction blister fluid but in dermal microdialysate NO was present at 44.3 ng per ml (SEM 6.2
42                             During ischemia, microdialysate norepinephrine concentrations increased i
43 ntrol and DSP-4-treated animals, hippocampal microdialysate norepinephrine concentrations were measur
44 -serine are simultaneously quantified in the microdialysate of an arctic ground squirrel to illustrat
45                         Analysis of in vitro microdialysates of hemolymph revealed more neuropeptides
46 a the PVN microdialysis probe did not affect microdialysate or plasma levels of the analytes at basel
47      In Group A, lactate levels in the donor microdialysate rose to >6 mM (P < 0.05), were significan
48 mine concentrations in rat prefrontal cortex microdialysate samples followed by administration of SKF
49      This method was used to analyze in vivo microdialysate samples from probes implanted in the stri
50         We first measured glutamate in 2 min microdialysate samples from the MPOA before, during, and
51 for determination of dopamine in 1-min brain microdialysate samples is described.
52 was identified in electropherograms of brain microdialysate samples obtained from anesthetized rats.
53 ted using the internal reference method from microdialysate samples that were obtained from two micro
54                                              Microdialysate samples were collected every 15 min.
55          In an additional series of 13 rats, microdialysate samples were obtained before, during, and
56 Dopamine was readily detected in 1-min brain microdialysate samples.
57 al cortex were measured in 20-min samples of microdialysate taken during a 2-hr baseline, 40 min of s
58                              On the basis of microdialysates, the proteomic data of lesional PSO and
59 M for lactate, based on a 20-muL conditioned microdialysate; these characteristics were sufficient to
60 l tissue tyrosine levels, but did not affect microdialysate tyrosine levels.
61 of biogenic monoamines in rat brain striatum microdialysates using capillary high-performance liquid
62             Basal NO concentration in dermal microdialysate was 0.60 +/- 0.14 microM (mean +/- s.e.m.
63                                          The microdialysate was brought to the entrance of the electr
64  3 h intervals, and the endorphin content of microdialysates was analyzed by a solid-phase radioimmun
65  concentrations in the blood and hippocampal microdialysate were determined by LC/MS-MS; NO productio
66 s in LNAA levels in brain tissue and in vivo microdialysate were generally comparable.
67  with PEGDE-based biosensors, and when brain microdialysates were analyzed, the levels of glutamate d
68                                              Microdialysates were collected hourly, then pooled (3-4
69 d peak concentrations of melatonin in AH-POA microdialysates within 20 min of injection (165 +/- 34 a