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1 ttenuated the anorectic response to amygdala enterostatin.
2 onists blocked the anorectic response to icv enterostatin.
3 amygdala that affect the feeding response to enterostatin.
4 tive l B) was injected into the PVN prior to enterostatin (0.01 nmol) injection into the amygdala.
5 ays recovery, rats were injected with either enterostatin (0.1 nmol) or saline vehicle (0.1 microl) i
6                                              Enterostatin (120 nmol, i.p.) reduced the intake of high
7 ced food intake (saline: 5.80 +/- 0.59 g vs. enterostatin 3.47 +/- 0.56 g, P < 0.05 at l h).
8 rily to release the N-terminal pentapeptide, enterostatin, a satiety factor.
9  provides the first anatomical evidence that enterostatin activates amygdala neurons that have functi
10                                              Enterostatin, an endogenous pentapeptide inhibits dietar
11                      The data imply that the enterostatin anorectic response may be modulated by 5-HT
12                         In vivo injection of enterostatin antibody into rat amygdala increased food i
13      These data suggest that procolipase and enterostatin are synthesized within specific regions of
14 and hypothalamic area that are responsive to enterostatin, by using a retrograde tracer fluorogold (F
15                                              Enterostatin did not alter [(3)H]-DA or [(3)H]-5HT relea
16                           We have shown that enterostatin enhanced [(3)H]-DA release, but not [(3)H]-
17  of central and peripheral administration of enterostatin (ENT) on food intake and gastric emptying o
18 ify which 5-HT receptor subtype mediates the enterostatin feeding behavior and whether this effect oc
19                                              Enterostatin has been shown to alter 5-HT release in the
20                      As central injection of enterostatin has potent effects on feeding, we hypothesi
21 526, 40 mg/kg body weight, i.p.) blocked the enterostatin hypophagic effects in these KO mice.
22 nalysis using antibodies for procolipase and enterostatin identified their immunoreactivity (IR) in r
23        Galanin, in doses of 25-300 pmol, and enterostatin, in doses of 0.5-10 nmol, were injected int
24                                          The enterostatin-induced increase in [(3)H]-DA release was b
25                                              Enterostatin IR was evident in the fibers of the dorsal
26                                              Enterostatin is a pentapeptide released from its precurs
27      The central mechanism for the action of enterostatin is not yet determined even though several m
28                  These findings suggest that enterostatin may inhibit dietary fat intake by blocking
29                   The effects of galanin and enterostatin on sympathetic activity have been examined
30        In rats fed a chow diet, injection of enterostatin produced only a transient 10% rise in firin
31                                              Enterostatin reduced food intake (saline: 5.80 +/- 0.59
32 y from the amygdala to the PVN regulates the enterostatin response through activation of 5-HTlB recep
33                                              Enterostatin selectively inhibits the intake of the diet
34  the feeding suppression induced by amygdala enterostatin, suggesting that there are functional conne

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