Development of psychophysiological motoric reactivity is influenced by peripubertal pharmacological inhibition of gonadotropin releasing hormone action – Results of an ovine model
Summary This study reports the effects of peripubertal GnRH receptor inactivation on development of psychophysiological motoric reactivity (PMR; sometimes also called emotional reactivity), plasma cortisol concentrations and the relationship between plasma cortisol and PMR in male and female sheep....
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Published in | Psychoneuroendocrinology Vol. 37; no. 11; pp. 1876 - 1884 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
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Elsevier Ltd
01.11.2012
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Abstract | Summary This study reports the effects of peripubertal GnRH receptor inactivation on development of psychophysiological motoric reactivity (PMR; sometimes also called emotional reactivity), plasma cortisol concentrations and the relationship between plasma cortisol and PMR in male and female sheep. The study formed part of a larger trial and utilised 46 same sex twins. One twin remained untreated (control) while the other received a subcutaneous GnRH agonist (GnRHa Goserelin-Acetate) implant every 4th week, beginning at 8 and 28 weeks of age, in males and females, respectively (different, due to sex specific age of puberty). PMR, a measure of an animals’ response to social isolation, was measured over a two minute period at 8, 28 and 48 weeks of age, using a three axis accelerometer. During the test period vocalisation rate was recorded. Cortisol was assayed in blood samples collected on a single day when animals were 40 weeks of age. PMR and vocalisation rate were significantly higher in females than males at all ages tested. At 28 weeks of age (20 weeks treatment) PMR was increased in treated males to the level seen in control females, by 48 weeks of age treated males’ PMR was significantly less than controls. In females, 20 weeks of GnRHa treatment (28–48 weeks of age) was not associated with differences in PMR. Cortisol concentrations were significantly higher in females than males but were not affected by treatment. Plasma cortisol concentrations were positively correlated with PMR; this relationship being driven by the treated animals in both sexes. The results demonstrate that PMR is sexually dimorphic and cortisol dependent in sheep from at least 8 weeks of age. Importantly, they also demonstrate that long-term treatment of males with a GnRH agonist results in changes in age-dependent development of PMR. |
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AbstractList | Summary This study reports the effects of peripubertal GnRH receptor inactivation on development of psychophysiological motoric reactivity (PMR; sometimes also called emotional reactivity), plasma cortisol concentrations and the relationship between plasma cortisol and PMR in male and female sheep. The study formed part of a larger trial and utilised 46 same sex twins. One twin remained untreated (control) while the other received a subcutaneous GnRH agonist (GnRHa Goserelin-Acetate) implant every 4th week, beginning at 8 and 28 weeks of age, in males and females, respectively (different, due to sex specific age of puberty). PMR, a measure of an animals’ response to social isolation, was measured over a two minute period at 8, 28 and 48 weeks of age, using a three axis accelerometer. During the test period vocalisation rate was recorded. Cortisol was assayed in blood samples collected on a single day when animals were 40 weeks of age. PMR and vocalisation rate were significantly higher in females than males at all ages tested. At 28 weeks of age (20 weeks treatment) PMR was increased in treated males to the level seen in control females, by 48 weeks of age treated males’ PMR was significantly less than controls. In females, 20 weeks of GnRHa treatment (28–48 weeks of age) was not associated with differences in PMR. Cortisol concentrations were significantly higher in females than males but were not affected by treatment. Plasma cortisol concentrations were positively correlated with PMR; this relationship being driven by the treated animals in both sexes. The results demonstrate that PMR is sexually dimorphic and cortisol dependent in sheep from at least 8 weeks of age. Importantly, they also demonstrate that long-term treatment of males with a GnRH agonist results in changes in age-dependent development of PMR. This study reports the effects of peripubertal GnRH receptor inactivation ondevelopment of psychophysiological motoric reactivity (PMR; sometimes also called emotionalreactivity), plasma cortisol concentrations and the relationship between plasma cortisol and PMRin male and female sheep.The study formed part of a larger trial and utilised 46 same sex twins. One twin remaineduntreated (control) while the other received a subcutaneous GnRH agonist (GnRHa Goserelin-Acetate) implant every 4th week, beginning at 8 and 28 weeks of age, in males and females,respectively (different, due to sex specific age of puberty). PMR, a measure of an animals’response to social isolation, was measured over a two minute period at 8, 28 and 48 weeks of age,using a three axis accelerometer. During the test period vocalisation rate was recorded. Cortisolwas assayed in blood samples collected on a single day when animals were 40 weeks of age.PMR and vocalisation rate were significantly higher in females than males at all ages tested. At28 weeks of age (20 weeks treatment) PMR was increased in treated males to the level seen incontrol females, by 48 weeks of age treated males’ PMR was significantly less than controls. Infemales, 20 weeks of GnRHa treatment (28—48 weeks of age) was not associated with differencesin PMR. Cortisol concentrations were significantly higher in females than males but were not affected by treatment. Plasma cortisol concentrations were positively correlated with PMR;this relationship being driven by the treated animals in both sexes.The results demonstrate that PMR is sexually dimorphic and cortisol dependent in sheepfrom at least 8 weeks of age. Importantly, they also demonstrate that long-term treatment ofmales with a GnRH agonist results in changes in age-dependent development of PMR. This study reports the effects of peripubertal GnRH receptor inactivation on development of psychophysiological motoric reactivity (PMR; sometimes also called emotional reactivity), plasma cortisol concentrations and the relationship between plasma cortisol and PMR in male and female sheep. The study formed part of a larger trial and utilised 46 same sex twins. One twin remained untreated (control) while the other received a subcutaneous GnRH agonist (GnRHa Goserelin-Acetate) implant every 4th week, beginning at 8 and 28 weeks of age, in males and females, respectively (different, due to sex specific age of puberty). PMR, a measure of an animals' response to social isolation, was measured over a two minute period at 8, 28 and 48 weeks of age, using a three axis accelerometer. During the test period vocalisation rate was recorded. Cortisol was assayed in blood samples collected on a single day when animals were 40 weeks of age. PMR and vocalisation rate were significantly higher in females than males at all ages tested. At 28 weeks of age (20 weeks treatment) PMR was increased in treated males to the level seen in control females, by 48 weeks of age treated males' PMR was significantly less than controls. In females, 20 weeks of GnRHa treatment (28-48 weeks of age) was not associated with differences in PMR. Cortisol concentrations were significantly higher in females than males but were not affected by treatment. Plasma cortisol concentrations were positively correlated with PMR; this relationship being driven by the treated animals in both sexes. The results demonstrate that PMR is sexually dimorphic and cortisol dependent in sheep from at least 8 weeks of age. Importantly, they also demonstrate that long-term treatment of males with a GnRH agonist results in changes in age-dependent development of PMR. This study reports the effects of peripubertal GnRH receptor inactivation on development of psychophysiological motoric reactivity (PMR; sometimes also called emotional reactivity), plasma cortisol concentrations and the relationship between plasma cortisol and PMR in male and female sheep. The study formed part of a larger trial and utilised 46 same sex twins. One twin remained untreated (control) while the other received a subcutaneous GnRH agonist (GnRHa Goserelin-Acetate) implant every 4th week, beginning at 8 and 28 weeks of age, in males and females, respectively (different, due to sex specific age of puberty). PMR, a measure of an animals’ response to social isolation, was measured over a two minute period at 8, 28 and 48 weeks of age, using a three axis accelerometer. During the test period vocalisation rate was recorded. Cortisol was assayed in blood samples collected on a single day when animals were 40 weeks of age. PMR and vocalisation rate were significantly higher in females than males at all ages tested. At 28 weeks of age (20 weeks treatment) PMR was increased in treated males to the level seen in control females, by 48 weeks of age treated males’ PMR was significantly less than controls. In females, 20 weeks of GnRHa treatment (28–48 weeks of age) was not associated with differences in PMR. Cortisol concentrations were significantly higher in females than males but were not affected by treatment. Plasma cortisol concentrations were positively correlated with PMR; this relationship being driven by the treated animals in both sexes. The results demonstrate that PMR is sexually dimorphic and cortisol dependent in sheep from at least 8 weeks of age. Importantly, they also demonstrate that long-term treatment of males with a GnRH agonist results in changes in age-dependent development of PMR. |
Author | Robinson, Jane E Haraldsen, Ira Ronit Hebold Erhard, Hans W Ropstad, Erik Fleming, Lynne M Evans, Neil P |
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CitedBy_id | crossref_primary_10_1016_j_psyneuen_2016_11_029 crossref_primary_10_1016_j_psyneuen_2013_03_009 crossref_primary_10_1111_jne_12048 crossref_primary_10_3389_fpsyg_2016_01053 crossref_primary_10_1016_j_psyneuen_2013_02_005 crossref_primary_10_1016_j_psyneuen_2013_09_011 crossref_primary_10_1016_j_psyneuen_2016_10_016 crossref_primary_10_1016_j_psyneuen_2019_06_008 crossref_primary_10_1371_journal_pone_0103607 crossref_primary_10_1111_apa_17150 crossref_primary_10_1016_j_bbr_2012_12_027 crossref_primary_10_1016_j_psyneuen_2013_11_005 crossref_primary_10_1159_000522087 |
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Keywords | Puberty GnRH agonist Emotional reactivity Sheep Cortisol Psychophysiological motoric reactivity GnRH Stress Affect affectivity Agonist Gonadotropin RH Hydrocortisone Glucocorticoid Development Inhibition Hormone releasing factor Ungulata Psychophysiology Corticosteroid Steroid hormone Antiinflammatory agent Emotion emotionality Hypothalamic hormone Vertebrata Mammalia Reactivity Animal Adrenal hormone Models Artiodactyla stress cortisol psychophysiological motoric reactivity puberty emotional reactivity sheep |
Language | English |
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Snippet | Summary This study reports the effects of peripubertal GnRH receptor inactivation on development of psychophysiological motoric reactivity (PMR; sometimes also... This study reports the effects of peripubertal GnRH receptor inactivation on development of psychophysiological motoric reactivity (PMR; sometimes also called... This study reports the effects of peripubertal GnRH receptor inactivation ondevelopment of psychophysiological motoric reactivity (PMR; sometimes also called... |
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SubjectTerms | Animal biology Animals Behavioral psychophysiology Biological and medical sciences Cortisol Emotional reactivity Emotions - drug effects Endocrinology & Metabolism Female Fundamental and applied biological sciences. Psychology GnRH GnRH agonist Gonadotropin-Releasing Hormone - antagonists & inhibitors Gonadotropin-Releasing Hormone - physiology Goserelin - pharmacology Hormones and behavior Hydrocortisone - blood Life Sciences Litter Size Male Motor Activity - drug effects Motor Activity - physiology Psychiatry Psychology. Psychoanalysis. Psychiatry Psychology. Psychophysiology Psychophysiological motoric reactivity Puberty Sex Factors Sexual Maturation - drug effects Sheep Sheep - growth & development Sheep - physiology Stress Vocalization, Animal - drug effects |
Title | Development of psychophysiological motoric reactivity is influenced by peripubertal pharmacological inhibition of gonadotropin releasing hormone action – Results of an ovine model |
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