ライフサイエンスコーパス: proestrous

1 imals infected in diestrus I or diestrus II (proestrous and estrous animals had less than 20% of infe

2 system can be considered more active during proestrous and following OVX since the output of luteini

3 alpha, 5alpha-THP in the PRF were greater in proestrous and hormone-primed rats, that are typically m

4 voked nocifensive behavior in female rats at proestrous and in OVX rats after E2 treatment.

5 of noradrenaline, and also in anaesthetised proestrous and ovariectomised rats following electrical

6 ccording to estrous stage (proestrous or non-proestrous) at the time of surgery.

7 VP exerted the same effects on diestrous and proestrous days of the ovarian cycle, whether hours befo

8 Regularly cycling, proestrous female rats received infusions of 200 ng of t

9 o cardiosomatic stimulation between male and proestrous female rats, despite differences in estradiol

10 rats, but this effect was most evident among proestrous female rats, which had the poorest spatial pe

11 ation in pentobarbital-anesthetized male and proestrous female rats.

12 naptic measures in gonadally intact male and proestrous female rats.

13 Proestrous females exhibited LF-LTP but males did not, s

14 Proestrous females had the highest microdialysate concen

15 ore DOR-labeled spines of pyramidal cells in proestrous females than males.

16 d, ovariectomized rats, lordosis behavior of proestrous females was less affected by VMN infusions wi

17 NTI blocked LF-LTP in proestrous females, but CTOP did not.

18 ncreased postsynaptic DORs mediate LF-LTP in proestrous females.

19 nal autoreceptor may exert a greater role in proestrous females; the serotonin transporter appears to

20 ls for metestrous (low estrogen) but not the proestrous (high estrogen) group.

21 es from ovariectomized (OVX), diestrous, and proestrous kisspeptin-GFP mice.

22 Proestrous levels of 3alpha-OH-THP reversed the deficits

23 A large proportion of GnRH cells in proestrous mice and very few GnRH cells in male mice exh

24 in GnRH cells is more pronounced in OVX and proestrous mice, the expression of galanin-IR in GnRH ce

25 d was increased across OVX --> diestrous --> proestrous mice.

26 rague Dawley rats that were nonpregnant (NP, proestrous), mid-pregnant (MP, days 9-10), late-pregnant

27 When slices were made from females on proestrous morning, when serum levels of 17beta-estradio

28 les were grouped according to estrous stage (proestrous or non-proestrous) at the time of surgery.

29 with kinetic modeling in female rats in the proestrous phase and after ovariectomy and in male rats.

30 he diestrous phase of the estrous cycle, the proestrous phase, and after ovariectomy.

31 n rats after ovariectomy than in rats in the proestrous phase.

32 just before (ZT10) the expected time of the proestrous preovulatory luteinizing hormone surge.

33 cysts and healthy uterus were harvested from proestrous rats and immunostained using the pan-neuronal

34 anserin and ketanserin, were investigated in proestrous rats and in ovariectomized rats hormonally pr

35 phase interacted with temperature such that proestrous rats performed better overall under the warm

36 In anaesthetised, proestrous rats receiving electrical stimulation no sign

37 Proestrous rats receiving intromissions (mated group) fr

38 In contrast, proestrous rats showed the largest response to methiothe

39 Proestrous rats were infused intraventricularly with eit

40 A group of proestrous rats were treated with phenoxybenzamine at do

41 Sexually receptive proestrous rats with bilateral cannulae in the ventromed

42 er, OFQ failed to produce antinociception in proestrous rats, the phase of the estrous cycle with the

43 re localized by immunoelectron microscopy in proestrous rats.

44 smaller responses were seen in diestrous and proestrous rats.

45 secretion, because alcohol also blocked the proestrous surge in adrenalectomized females.

46 tral reproductive endocrine event; i.e., the proestrous surge of gonadotropins, which triggers ovulat

47 Alcohol administration blocked the proestrous surge of LH and ovulation.

48 the magnitude of the decline was smaller in proestrous than in hormone-primed, ovariectomized rats.

49 vastly more prevalent in the spinal cord of proestrous vs. diestrous females and vs. males.