dc.description.abstract |
Neuropeptide Y (NPY) acts at the hypothalamus to regulate the reproductive function by
stimulating the release of GnRH from hypothalamus. In the present study a group of 5
female adult rhesus monkeys (Macaca mulatta), 5.5-9 years old, mean body weight of
10.31±0.90 kg and with menstrual cycle of 31 days was used. Changes in their body
weight, behavior and sex skin color were observed throughout the cycle. Menstrual cycle
of each monkey was monitored daily by recording the onset and duration of menstrual
bleeding with vaginal swabs. Baseline profile of estradiol (E2), progesterone (P),
prolactin (PRL) and growth hormone (GH) were measured by collecting blood sample (2
ml) on different days throughout the menstrual cycle of 31 days. Sequential blood
samples (2 ml) were collected at an interval of 15 minutes for one hour before NPY
administration for the hormonal baseline and for 2 hours and 15 minutes after NPY
administration. In order to study the effect of NPY on plasma E2, P, PRL and GH levels
on day 1 (menstrual phase), day 7 (follicular phase), day 15 (peri-ovulatory phase) and
day 21 (luteal phase) of menstrual cycle, 200 μg of NPY in single bolus intravenous
injection was given. Individual and mean body weight during the menstrual cycle was not
significantly different. After NPY administration monkeys were relaxed and comfortable.
Sex skin coloration changed progressively from whitish pink to deep red following
menstrual to periovulatory phase and then decrease in colour intensity occurred during
luteal phase. Baseline profile of estradiol showed that plasma E2 concentration was
significantly high (P<0.001) in the periovulatory phase of menstrual cycle compared to
menstrual, follicular and luteal phases. The luteal phase plasma E2 level was significantly
low compared to follicular phase (P<0.003) but not significantly different from the
menstrual phase. Plasma estradiol level 15 minutes after NPY administration increased
non-significantly in all the four phases of menstrual cycle compared to baseline at 0
minute. Then, subsequent significant temporal increase till 45 minutes on day 1, 75
minutes on day 15, 60 minutes on day 7 and day 21 followed by subsequent significant
temporal decrease. At the end of experiment plasma estradiol attained the basal level in
all the four phases. Baseline profile of plasma progesterone showed significantly low
levels during menstrual, follicular and periovulatory phases compared to the luteal phase.
No significant difference was observed in the plasma P concentration between menstrual,
follicular, and ovulatory phases. In all the four phases of menstrual cycle plasma
progesterone level 15 minutes after NPY administration increased non-significantly
followed by significant temporal increase till 60 minutes on day 1, 105 minutes on day 7,
135 minutes (i.e. till the end of experiment) on day 15 and 30 minutes on day 21. After
then non-significant temporal decrease on day 7 and significant on day 1 (P<0.0002) and
day 21 (P<0.0007) was observed. The baseline profile of plasma PRL showed that
plasma PRL levels were significantly high during menstrual (P<0.013) and periovulatory
phases (P<0.023) compared to luteal phase. Plasma prolactin level of follicular phase was
non-significantly lower than menstrual and peri-ovulatory phases. The plasma prolactin
levels of follicular and luteal phases were not different. In plasma prolactin concentration
after 15 minutes of NPY bolus injection a non-significant rise was observed on day 1
followed by non-significant temporal increase till 30 minutes and then significant
temporal decrease till the end of experiment. On day 7 non-significant and on day 15
significant increase in plasma prolactin level was observed 15 minutes after NPY
administration followed by significant temporal decrease on day 7 (P<0.0005) and day 15
(P<0.009). On day 21 a non-significant decrease in plasma prolactin level after 15
minutes of NPY administration followed by significant temporal decreased till the end of
experiment. Regression analysis of variance showed highly significant temporal decrease
(P<0.0003). The base line plasma in all the four phases of menstrual cycle GH levels in
all the four phases of menstrual cycle were non-significantly different (P>0.05). NPY
administration inhibited the plasma GH level in all the four phases of menstrual cycle. On
day 1 (menstrual phase) of menstrual cycle plasma growth hormone level 15 minutes
after NPY administration decreased non-significantly with subsequent non-significant
temporal decrease till 45 minutes followed by significant temporal increase till the end of
experiment. A highly significant decrease in plasma GH level was observed on day 7
(follicular phase) and non-significantly on day 15 (periovulatory phase) and day 21
(luteal phase) of menstrual cycle 15 minutes after NPY administration followed by non-
significant temporal decrease on day 7 and day 15, but significant temporal decrease on
day 21 (P<0.004) till the end of experiment. These results show that NPY has stimulatory
and inhibitory effects on the ovarian and pituitary hormones by acting as a modulator,
neurotransmitter and neurohormone. NPY has applications in pharmacological fields and
can be used for further research. |
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