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IOSR Journal of Mathematics (IOSR-JM)
e-ISSN: 2278-5728, p-ISSN: 2319-765X. Volume 13, Issue 1 Ver. II (Jan. - Feb. 2017), PP 39-42
www.iosrjournals.org
DOI: 10.9790/5728-1301023942 www.iosrjournals.org 39 | Page
Mathematical Model for Secretion of Leptin, Growth Hormone
and Luteinizing Hormone
Geetha .T* and Sangeetha.B**
*Asst professor of mathematics K.N Govt Arts college for women, Thanjavur. Tamilnadu, Southindia.
**Lecturer of mathematics, BDU college Orathanadu, Thanjavur, Tamilnadu, Southindia
Abstract: Estimation of r when y is censored at x was applied to altered secretion of leptin,growth hormone
and luteinizing hormone after 84 h of sustained physical exertion super imposed on caloric and sleep
restriction an estimator based on a maximum likelihood estimates(MLEs) for reliability when stress is censored
at strength. We assume that X is a random strength of a component subjected to a random stress (Y) and
reliability of a component is given by R=P[Y < X],where (X,Y) follows the bivariate exponential (BVE) model of
Marshall-Olkin.
Keywords: Bivariate exponential model, Maximum likelihood estimate, GH,LH.
I. Introduction
The pulsatile release of growth hormone (GH) and luteinizing hormone (LH) from the anterior pituitary
gland is integral for signaling secretion of insulin-like growth factor (IGF)-I and testosterone, respectively. This
study examined the hypothesis that 84 h of sustained physical exertion with caloric and sleep restriction alters
the secretion of GH and LH. The pulsatile release of GH and LH from the anterior pituitary gland is integral for
the trophic effects that these hormones exert on IGF-I and testosterone, respectively.The manner in which
anterior pituitary hormones are released and delivered to target tissues is more biologically significant than the
overall mean hormonal concentrations was well illustrated by Isgaard et al. , who demonstrated that GH
administered in a pulsatile manner elicited greater increases in IGF-I than GH administered in a continuous
manner. Because of the episodic release pattern of GH and LH, multiple time-point measures are necessary to
fully characterize the trophic effects these hormones may have. Although alterations in IGF-I and testosterone are known to
be mediated by fluctuations in GH and LH, few studies have concomitantly measured these hormones, especially in healthy
subjects exposed to multiple physiological stressors. Military operational scenarios represent a unique paradigm in which to
study endocrine responses to metabolic stress. Soldiers, analogous to emergency rescue personnel and ultra endurance
athletes are often required to perform heavy sustained physical exertion in the face of nutritional and sleep deprivation. Prior
work on military populations has shown that continued and prolonged exposure to such physiological strain can lead to a
suppression of circulating anabolic growth factors, losses of lean body mass, increased susceptibility to disease and
infections, and diminished physical and cognitive performance capabilities.Fourteen healthy male soldiers volunteered to
participate in the study. Three injuries and one illness prevented four of these test subjects from completing the study. The
data from the remaining 10volunteers [22 yr (SD 3), 183 cm (SD 7), 87 kg (SD 8)] are presented in this paper. The
experiment was approved by the appropriate Institutional Scientific Review and Human Use Review
Committees.The subjects were briefed on the study procedures, and written consent was obtained before study
participation. Mean GH concentration was significantly increased after military stress compared with the control
condition. The increase in mean GH concentration was accompanied by an increase in the following secretion
parameters: area under bursts, amplitude of bursts, basal secretion rate, overnight basal secretion, overnight
pulsatile secretion, and total overnight secretion. GH half-life, number of bursts, interval between bursts, and
amplitude of largest burst were similar between the control and military operational stress conditions
Mathematical Model for Secretion of Leptin,Growth Hormone and Luteinizing Hormone
DOI: 10.9790/5728-1301023942 www.iosrjournals.org 40 | Page
Mean concentration of all subjects over the 12-h sampling period.Samples were taken every 20 min for a total of
36 blood draws as represented on the x-axis. Main effect mean concentrations of GH (A), LH (B), and leptin(C)
after the military stress condition are statistically different (P≤0.05) from control for all hormones
The fact that short-term (4 days) military operational stress can have striking effects on the
neuroendocrine system raises questions for future studies concerning the potential adverse impact of long-term
military operational stress on soldier physiology and the subsequent health and fitness of our military
personnel.This study used a rigorous serial blood sampling scheme and subsequent time-series deconvolution
analyses to assess GH and LH secretion patterns. These data expand on prior research that relied on one time-
point blood samples to glean informationon the endocrine responses to stress that are subject to episodic and
circadian release patterns.The physiological significance of studying the pulsatile release of these hormones lies
in the fact that the episodic release pattern is thought to be integral in eliciting optimal agonist function at the
cellular level.The salient finding emerging from this study was an amplification of GH and LH secretion with a
concomitant decline in IGF-I and testosterone. Because GH and LH are known to positively regulate IGF-I and
testosterone, these data imply that the physiological strain experienced in this study induced a certain degree of
peripheral resistance.
Despite enhanced release of LH, testosterone concentrations decreased. During the 12-h overnight
sampling period, total and free testosterone concentrations were 24 and 30% lower after the military stress
condition, respectively. By considering the circadian rhythm of testosterone, our study has extended these
findings by demonstrating that testosterone concentrations are decreased and remain depressed overnight for a
12-h period following the conclusion of a multiple-day military stress condition. compared with younger men,
older men tend to possess greater LH secretion, which is hypothesized to represent a biological attempt to
maintain normal testosterone concentrations.Endurance-trained athletes have also shown decreased testosterone
and increased LH concentrations.The literature with regard to acute exercise stress has been equivocal. Thus,
although LH pulsatility is slowly restored in women, there is evidence to suggest that gonadotropin releasing
hormone neurons may rapidly respond to caloric intake. Leptin concentrations declined from 3.8 to 2.0 ng/ml
after military stress. These declines were coincident with marked reductions in fat mass and increased
concentrations of circulating free fatty acids (33%). This magnitude decrease for leptin is consistent with the
44% decrease reported by Maccario et al.After 36 h of fasting, but less than the 66% decline observed by
Gomez-Merino et al. fter a 5-day military combat course. These changes are reflective of substantial lipolytic
activity. Also of interest is the fact that the overall main effect mean for glucose concentrations was similar
between the control and military stress condition, suggesting that glucose homeostasis was well defended in this
paradigm. Although not measured in the present study, other studies have reported robust changes in cortisol
after military stress , and it is also probable that both cortisol and catecholamine elevations played a contribution
in maintaining glucose concentrations. The fact that the absolute losses in fat-free mass and fat mass were
similar suggests that amino acid fuel partially contributed to gluconeogenesis. Converging lines of evidence in
sheep, rat, monkey, and human models suggest that leptin acts as a peripheral signal to mediate metabolic
regulation of GH and LH secretion from the anterior pituitary gland. Leptin appears to prevent the fasting-
induced suppression of pulsatile release of LH secretion. In a recent study that evaluated the effects of differing
doses of exogenously administered Leptin in men during 73 h of fasting and employing 24-h blood sampling,
Chan et al. demonstrated a role for leptin in normalizing starvation-induced neuroendocrine changes, notably the
hypothalamic- pituitary-gonadal axis. Chan et al. hypothesized that a threshold leptin level between 0.5 and 2.0
ng/ml may be necessary for LH secretion.Although glucose concentrations have also been speculated to act as a
peripheral signal relaying information concerning nutritional status and within the context of the dramatic
hormonal changes observed , it is remarkable that glucosehomeostasis was well maintained.
II. Mathematical Model
Let {(xi,yi)}be an i.i.d.random sample of size n from BVE of Marshall Olkin(1967). The strength and stress
associated with the i-th pair of the Sample is
(Xi,Yi) = (xi,xi) if xi  yi
= (xi,xi) if xi > yi
The likelihood of the sample of size n is












  
21
1
2
1
1
n
i
n
i
ffL
Where
i
i
x x
XYxNXP
f
i 



),([
lim
0
1
Mathematical Model for Secretion of Leptin,Growth Hormone and Luteinizing Hormone
DOI: 10.9790/5728-1301023942 www.iosrjournals.org 41 | Page
=    ix  exp31 ,
ii
ii
yx yx
XYyNYxNXP
f
ii 



),(),([
lim
0,0
2
=     ii xy 312312 exp   ,
n1(or n2) is the number of observations with xi  yi (or xi > yi) in the sample of size n = n1+n2.
XN(xi) [ or Y N(yi)] denotes X(or Y ) fall in the neighborhood of xi(or yi)i.e.,xi<X< xi+ δxi, for a small
increment δ around xi(or yi< Y< yi + δyi, for a small increment δ around yi). The expected values of n1 and n2 are
E(n1)= (1+3)/  and E(n2)= 2 / .
Letting = 1+3, the above like hood can be written as
L =






  
n
i
ii
n
i
i
nn
yxx
11
22 ),min(exp2

It is observed from the above expression that we have complete observations on X and Min(X,Y) in this
censored scheme. It is a very important feature in the case of stress censored at strength. The like hood equations
with respect to the parameters (2, ) are
n2/2 = 
n
i
ii yx
1
),min(
n/γ = 
n
i
ix
1
The MLEs of (⋋2 ,γ) are


n
i ii yxMinn 122 ),(/ˆ and 

n
i ixMinn 1
/ˆ
One important observation here is that we have closed form expressions for the MLEs of (⋋2 γ) in this
censored scheme but in the complete sample scheme the MLES of the parameters do not have explicit
expressions and can be obtained by either by Newton-Raphson procedure or Fisher’s method of scoring. [See
Hangal and Kale(1991)].
The asymptotic variance-covariance matrix of ((⋋2 Ύ) is
V( 2
ˆ )= ⋋2⋋/n,V (ˆ ) = γ2
/n and Cov ( 2
ˆ ,ˆ ) =0.
Now the MLE of R is given by )ˆˆ/(ˆˆ
221  R and its asymptotic distributions is AN[R,R(1-
R)2
(1+R)/n]. Jana (1994) obtained the estimate of R based on the complete sample on X and Min(X,Y); i.e.,
 

n
i i
n
i ii xyxR 112 /),min(1ˆ , which is AN[R,2R(1-R)2
/n].One can also have an estimator based on
count n2 which is binomial(n,R).The natural estimateor of R is nnR /ˆ
23 which is AN[R,R(1-R)/n].
The asymptotic relative efficiency (ARE) of the estimator iRˆ to the estimator jRˆ is given by
ARE  ji RR ˆ,ˆ = var( jRˆ ) / var( iRˆ ) i j = 1,2,3
The estimator 1
ˆR is more efficient as compared to 2
ˆR and 3
ˆR . The estimator 2
ˆR is more than efficient than the
estimator 3
ˆR when R > .5, 3
ˆR is more efficient than 2
ˆR when R <.5, and both are equally efficient when R=.5.
X F1 F2
0.2 0.1802 0.1120
0.4 0.0483 0.0503
0.6 0.0129 0.0237
0.8 0.0035 0.0114
1 0.0009 0.0055
1.2 0.0002 0.0026
1.4 0.0001 0.0013
1.6 0.000018 0.0036
1.8 0.000005 0.0017
2 0.000001 0.0027
Mathematical Model for Secretion of Leptin,Growth Hormone and Luteinizing Hormone
DOI: 10.9790/5728-1301023942 www.iosrjournals.org 42 | Page
Likelihood of leptin = 0
Reliability of leptin = 0.8978
III. Conclusion
That short-term military operational stress can exert marked effects in neuroendocrine secretion
patterns raises important questions concerning the potential adverse effects on longer-term military operational
stress on underlying physiology and metabolism and the health status of military personnel and also found
likelihood of sample for 36 size of leptin.
References
[1]. Castellani JW, Stulz DA, Degroot DW, Blanchard LA, Cadarette BS, Nindl BC, and Montain SJ. 84 hours of sustained
operations alter thermoregulation during cold exposure. Med Sci Sports Exerc 35: 175– 181, 2003.
[2]. Friedl KE, Moore RJ, Martinez-Lopez LE, Vogel JA, Askew EW, Marchitelli LJ, Hoyt RW, and Gordon CC. Lower limit of
body fat in healthy men. J Appl Physiol 77: 933–940, 1994.
[3]. Friedl KE, Moore RJ, Hoyt RW, Marchitelli LJ, Martinez-Lopez LE, and Askew W. Endocrine markers of semistarvation in
healthy lean men in a multistressor environment. J Appl Physiol 88: 1820–1830, 2000
[4]. Hanagal, D.D.(1995). Testing reliability in a bivariate exponentialstress-strength model. Journal of the Indian StatisticalAssociation,
33, 41-45.
[5]. Johnson ML, Virostko A, Veldhuis JD, and Evans WS. Deconvolution analysis as a hormone pulse-detection algorithm.
Methods Enzymol 384: 40–54, 2004.
[6]. Kramer TR, Moore RJ, RL Shippee, KE Friedl, L Martinez-Lopez, MM Chan, and Askew EW. Effects of food restriction in
military training on T-lymphocyte responses. Int J Sports Med 18: 84–90, 1997.
[7]. Marshall, A.W. and Olkin, I.(1967). A multivariate exponential distribution. Journal of the American Statistical Association, 62, 30-
44.
[8]. Nindl BC, Friedl KE, Frykman PN, Marchitelli LJ, Shippee RL, and Patton JF. Physical performance and metabolic recovery
among lean, healthy men following a prolonged energy deficit. Int J Sports Med 18: 317–324, 1997.
[9]. Veldhuis JD, Anderson SM, Shah N, Bray M, Vick T, Gentili A, Mulligan T, Johnson ML, Weltman A, Evans WS, and
Iranmanesh A. Neurophysiological regulation and target-tissue impact of the pulsatile mode of growth hormone secretion in the
human. Growth Horm IGF Res 11, Suppl A: 25–37, 2001
[10]. Veldhuis JD. Issues in quantifying pulsatile neurohormone release. In:Methods in Neuroendocrinology. Baton Rouge, FL: CRC,
1998, p. 181–203

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Mathematical Model for Secretion of Leptin, Growth Hormone and Luteinizing Hormone

  • 1. IOSR Journal of Mathematics (IOSR-JM) e-ISSN: 2278-5728, p-ISSN: 2319-765X. Volume 13, Issue 1 Ver. II (Jan. - Feb. 2017), PP 39-42 www.iosrjournals.org DOI: 10.9790/5728-1301023942 www.iosrjournals.org 39 | Page Mathematical Model for Secretion of Leptin, Growth Hormone and Luteinizing Hormone Geetha .T* and Sangeetha.B** *Asst professor of mathematics K.N Govt Arts college for women, Thanjavur. Tamilnadu, Southindia. **Lecturer of mathematics, BDU college Orathanadu, Thanjavur, Tamilnadu, Southindia Abstract: Estimation of r when y is censored at x was applied to altered secretion of leptin,growth hormone and luteinizing hormone after 84 h of sustained physical exertion super imposed on caloric and sleep restriction an estimator based on a maximum likelihood estimates(MLEs) for reliability when stress is censored at strength. We assume that X is a random strength of a component subjected to a random stress (Y) and reliability of a component is given by R=P[Y < X],where (X,Y) follows the bivariate exponential (BVE) model of Marshall-Olkin. Keywords: Bivariate exponential model, Maximum likelihood estimate, GH,LH. I. Introduction The pulsatile release of growth hormone (GH) and luteinizing hormone (LH) from the anterior pituitary gland is integral for signaling secretion of insulin-like growth factor (IGF)-I and testosterone, respectively. This study examined the hypothesis that 84 h of sustained physical exertion with caloric and sleep restriction alters the secretion of GH and LH. The pulsatile release of GH and LH from the anterior pituitary gland is integral for the trophic effects that these hormones exert on IGF-I and testosterone, respectively.The manner in which anterior pituitary hormones are released and delivered to target tissues is more biologically significant than the overall mean hormonal concentrations was well illustrated by Isgaard et al. , who demonstrated that GH administered in a pulsatile manner elicited greater increases in IGF-I than GH administered in a continuous manner. Because of the episodic release pattern of GH and LH, multiple time-point measures are necessary to fully characterize the trophic effects these hormones may have. Although alterations in IGF-I and testosterone are known to be mediated by fluctuations in GH and LH, few studies have concomitantly measured these hormones, especially in healthy subjects exposed to multiple physiological stressors. Military operational scenarios represent a unique paradigm in which to study endocrine responses to metabolic stress. Soldiers, analogous to emergency rescue personnel and ultra endurance athletes are often required to perform heavy sustained physical exertion in the face of nutritional and sleep deprivation. Prior work on military populations has shown that continued and prolonged exposure to such physiological strain can lead to a suppression of circulating anabolic growth factors, losses of lean body mass, increased susceptibility to disease and infections, and diminished physical and cognitive performance capabilities.Fourteen healthy male soldiers volunteered to participate in the study. Three injuries and one illness prevented four of these test subjects from completing the study. The data from the remaining 10volunteers [22 yr (SD 3), 183 cm (SD 7), 87 kg (SD 8)] are presented in this paper. The experiment was approved by the appropriate Institutional Scientific Review and Human Use Review Committees.The subjects were briefed on the study procedures, and written consent was obtained before study participation. Mean GH concentration was significantly increased after military stress compared with the control condition. The increase in mean GH concentration was accompanied by an increase in the following secretion parameters: area under bursts, amplitude of bursts, basal secretion rate, overnight basal secretion, overnight pulsatile secretion, and total overnight secretion. GH half-life, number of bursts, interval between bursts, and amplitude of largest burst were similar between the control and military operational stress conditions
  • 2. Mathematical Model for Secretion of Leptin,Growth Hormone and Luteinizing Hormone DOI: 10.9790/5728-1301023942 www.iosrjournals.org 40 | Page Mean concentration of all subjects over the 12-h sampling period.Samples were taken every 20 min for a total of 36 blood draws as represented on the x-axis. Main effect mean concentrations of GH (A), LH (B), and leptin(C) after the military stress condition are statistically different (P≤0.05) from control for all hormones The fact that short-term (4 days) military operational stress can have striking effects on the neuroendocrine system raises questions for future studies concerning the potential adverse impact of long-term military operational stress on soldier physiology and the subsequent health and fitness of our military personnel.This study used a rigorous serial blood sampling scheme and subsequent time-series deconvolution analyses to assess GH and LH secretion patterns. These data expand on prior research that relied on one time- point blood samples to glean informationon the endocrine responses to stress that are subject to episodic and circadian release patterns.The physiological significance of studying the pulsatile release of these hormones lies in the fact that the episodic release pattern is thought to be integral in eliciting optimal agonist function at the cellular level.The salient finding emerging from this study was an amplification of GH and LH secretion with a concomitant decline in IGF-I and testosterone. Because GH and LH are known to positively regulate IGF-I and testosterone, these data imply that the physiological strain experienced in this study induced a certain degree of peripheral resistance. Despite enhanced release of LH, testosterone concentrations decreased. During the 12-h overnight sampling period, total and free testosterone concentrations were 24 and 30% lower after the military stress condition, respectively. By considering the circadian rhythm of testosterone, our study has extended these findings by demonstrating that testosterone concentrations are decreased and remain depressed overnight for a 12-h period following the conclusion of a multiple-day military stress condition. compared with younger men, older men tend to possess greater LH secretion, which is hypothesized to represent a biological attempt to maintain normal testosterone concentrations.Endurance-trained athletes have also shown decreased testosterone and increased LH concentrations.The literature with regard to acute exercise stress has been equivocal. Thus, although LH pulsatility is slowly restored in women, there is evidence to suggest that gonadotropin releasing hormone neurons may rapidly respond to caloric intake. Leptin concentrations declined from 3.8 to 2.0 ng/ml after military stress. These declines were coincident with marked reductions in fat mass and increased concentrations of circulating free fatty acids (33%). This magnitude decrease for leptin is consistent with the 44% decrease reported by Maccario et al.After 36 h of fasting, but less than the 66% decline observed by Gomez-Merino et al. fter a 5-day military combat course. These changes are reflective of substantial lipolytic activity. Also of interest is the fact that the overall main effect mean for glucose concentrations was similar between the control and military stress condition, suggesting that glucose homeostasis was well defended in this paradigm. Although not measured in the present study, other studies have reported robust changes in cortisol after military stress , and it is also probable that both cortisol and catecholamine elevations played a contribution in maintaining glucose concentrations. The fact that the absolute losses in fat-free mass and fat mass were similar suggests that amino acid fuel partially contributed to gluconeogenesis. Converging lines of evidence in sheep, rat, monkey, and human models suggest that leptin acts as a peripheral signal to mediate metabolic regulation of GH and LH secretion from the anterior pituitary gland. Leptin appears to prevent the fasting- induced suppression of pulsatile release of LH secretion. In a recent study that evaluated the effects of differing doses of exogenously administered Leptin in men during 73 h of fasting and employing 24-h blood sampling, Chan et al. demonstrated a role for leptin in normalizing starvation-induced neuroendocrine changes, notably the hypothalamic- pituitary-gonadal axis. Chan et al. hypothesized that a threshold leptin level between 0.5 and 2.0 ng/ml may be necessary for LH secretion.Although glucose concentrations have also been speculated to act as a peripheral signal relaying information concerning nutritional status and within the context of the dramatic hormonal changes observed , it is remarkable that glucosehomeostasis was well maintained. II. Mathematical Model Let {(xi,yi)}be an i.i.d.random sample of size n from BVE of Marshall Olkin(1967). The strength and stress associated with the i-th pair of the Sample is (Xi,Yi) = (xi,xi) if xi  yi = (xi,xi) if xi > yi The likelihood of the sample of size n is                21 1 2 1 1 n i n i ffL Where i i x x XYxNXP f i     ),([ lim 0 1
  • 3. Mathematical Model for Secretion of Leptin,Growth Hormone and Luteinizing Hormone DOI: 10.9790/5728-1301023942 www.iosrjournals.org 41 | Page =    ix  exp31 , ii ii yx yx XYyNYxNXP f ii     ),(),([ lim 0,0 2 =     ii xy 312312 exp   , n1(or n2) is the number of observations with xi  yi (or xi > yi) in the sample of size n = n1+n2. XN(xi) [ or Y N(yi)] denotes X(or Y ) fall in the neighborhood of xi(or yi)i.e.,xi<X< xi+ δxi, for a small increment δ around xi(or yi< Y< yi + δyi, for a small increment δ around yi). The expected values of n1 and n2 are E(n1)= (1+3)/  and E(n2)= 2 / . Letting = 1+3, the above like hood can be written as L =          n i ii n i i nn yxx 11 22 ),min(exp2  It is observed from the above expression that we have complete observations on X and Min(X,Y) in this censored scheme. It is a very important feature in the case of stress censored at strength. The like hood equations with respect to the parameters (2, ) are n2/2 =  n i ii yx 1 ),min( n/γ =  n i ix 1 The MLEs of (⋋2 ,γ) are   n i ii yxMinn 122 ),(/ˆ and   n i ixMinn 1 /ˆ One important observation here is that we have closed form expressions for the MLEs of (⋋2 γ) in this censored scheme but in the complete sample scheme the MLES of the parameters do not have explicit expressions and can be obtained by either by Newton-Raphson procedure or Fisher’s method of scoring. [See Hangal and Kale(1991)]. The asymptotic variance-covariance matrix of ((⋋2 Ύ) is V( 2 ˆ )= ⋋2⋋/n,V (ˆ ) = γ2 /n and Cov ( 2 ˆ ,ˆ ) =0. Now the MLE of R is given by )ˆˆ/(ˆˆ 221  R and its asymptotic distributions is AN[R,R(1- R)2 (1+R)/n]. Jana (1994) obtained the estimate of R based on the complete sample on X and Min(X,Y); i.e.,    n i i n i ii xyxR 112 /),min(1ˆ , which is AN[R,2R(1-R)2 /n].One can also have an estimator based on count n2 which is binomial(n,R).The natural estimateor of R is nnR /ˆ 23 which is AN[R,R(1-R)/n]. The asymptotic relative efficiency (ARE) of the estimator iRˆ to the estimator jRˆ is given by ARE  ji RR ˆ,ˆ = var( jRˆ ) / var( iRˆ ) i j = 1,2,3 The estimator 1 ˆR is more efficient as compared to 2 ˆR and 3 ˆR . The estimator 2 ˆR is more than efficient than the estimator 3 ˆR when R > .5, 3 ˆR is more efficient than 2 ˆR when R <.5, and both are equally efficient when R=.5. X F1 F2 0.2 0.1802 0.1120 0.4 0.0483 0.0503 0.6 0.0129 0.0237 0.8 0.0035 0.0114 1 0.0009 0.0055 1.2 0.0002 0.0026 1.4 0.0001 0.0013 1.6 0.000018 0.0036 1.8 0.000005 0.0017 2 0.000001 0.0027
  • 4. Mathematical Model for Secretion of Leptin,Growth Hormone and Luteinizing Hormone DOI: 10.9790/5728-1301023942 www.iosrjournals.org 42 | Page Likelihood of leptin = 0 Reliability of leptin = 0.8978 III. Conclusion That short-term military operational stress can exert marked effects in neuroendocrine secretion patterns raises important questions concerning the potential adverse effects on longer-term military operational stress on underlying physiology and metabolism and the health status of military personnel and also found likelihood of sample for 36 size of leptin. References [1]. Castellani JW, Stulz DA, Degroot DW, Blanchard LA, Cadarette BS, Nindl BC, and Montain SJ. 84 hours of sustained operations alter thermoregulation during cold exposure. Med Sci Sports Exerc 35: 175– 181, 2003. [2]. Friedl KE, Moore RJ, Martinez-Lopez LE, Vogel JA, Askew EW, Marchitelli LJ, Hoyt RW, and Gordon CC. Lower limit of body fat in healthy men. J Appl Physiol 77: 933–940, 1994. [3]. Friedl KE, Moore RJ, Hoyt RW, Marchitelli LJ, Martinez-Lopez LE, and Askew W. Endocrine markers of semistarvation in healthy lean men in a multistressor environment. J Appl Physiol 88: 1820–1830, 2000 [4]. Hanagal, D.D.(1995). Testing reliability in a bivariate exponentialstress-strength model. Journal of the Indian StatisticalAssociation, 33, 41-45. [5]. Johnson ML, Virostko A, Veldhuis JD, and Evans WS. Deconvolution analysis as a hormone pulse-detection algorithm. Methods Enzymol 384: 40–54, 2004. [6]. Kramer TR, Moore RJ, RL Shippee, KE Friedl, L Martinez-Lopez, MM Chan, and Askew EW. Effects of food restriction in military training on T-lymphocyte responses. Int J Sports Med 18: 84–90, 1997. [7]. Marshall, A.W. and Olkin, I.(1967). A multivariate exponential distribution. Journal of the American Statistical Association, 62, 30- 44. [8]. Nindl BC, Friedl KE, Frykman PN, Marchitelli LJ, Shippee RL, and Patton JF. Physical performance and metabolic recovery among lean, healthy men following a prolonged energy deficit. Int J Sports Med 18: 317–324, 1997. [9]. Veldhuis JD, Anderson SM, Shah N, Bray M, Vick T, Gentili A, Mulligan T, Johnson ML, Weltman A, Evans WS, and Iranmanesh A. Neurophysiological regulation and target-tissue impact of the pulsatile mode of growth hormone secretion in the human. Growth Horm IGF Res 11, Suppl A: 25–37, 2001 [10]. Veldhuis JD. Issues in quantifying pulsatile neurohormone release. In:Methods in Neuroendocrinology. Baton Rouge, FL: CRC, 1998, p. 181–203