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      24-hour changes in circulating prolactin, follicle-stimulating hormone, luteinizing hormone and testosterone in male rats subjected to social isolation

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          Abstract

          Background

          This work analyzes the effect of social isolation (a mild stressor) on the 24-h variation of pituitary-testicular function in young Wistar rats, assessed by measuring circulating levels of prolactin, FSH, LH and testosterone.

          Methods

          Animals were either individually caged or kept in groups (4–5 animals per cage) under a 12:12 h light-dark cycle (lights on at 0800 h) for 30 days starting on day 35 of life. Rats were killed at 4-h intervals during a 24-h cycle, beginning at 0900 h.

          Results

          Isolation brought about a decrease in prolactin, LH and testosterone secretion and an increase of FSH secretion. In isolated rats the 24-h secretory pattern of prolactin and testosterone became modified, i.e., the maximum in prolactin seen in control animals at the beginning of the activity span was no longer detected, whereas the maximum in circulating testosterone taking place at 1700 h in controls was phase-delayed to 2100 h in isolated rats.

          Conclusion

          Social isolation affects the 24-h variation of pituitary-testicular function in young rats. Secretion of prolactin, LH and testosterone decreases, and secretion of FSH increases, in isolated rats. The maximum in prolactin seen in group-caged rats at the beginning of the activity span is not observed in isolated rats. The maximum in circulating testosterone taking place at the second part of the rest span in controls is phase-delayed to the light-dark transition in isolated rats.

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          Most cited references36

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          Effect of stress on the activity of the hypothalamic-pituitary-gonadal axis: peripheral and central mechanisms.

          This article reviews the mechanisms believed to mediate stress-induced inhibition of reproductive functions and the anatomical sites at which these effects take place. Particular emphasis is placed on the potential modulating role of hormones or neurotransmitters released during stress. At the level of the gonads, adrenal corticoids, pro-opiomelanocortin (POMC)-like peptides, and corticotropin-releasing factor (CRF) are reported to interfere with the stimulatory action of gonadotropins on sex steroid-producing cells. Increased circulating corticosteroid levels may also decrease pituitary responsiveness to GnRH. There is, however, increasing evidence that these mechanisms are primarily involved in mediating the effects of prolonged stress, but not those of an acute stimulus. In contrast, a variety of hormones or neurotransmitters, including CRF, POMC peptides, and biogenic amines act within the brain to mediate the inhibitory influence of both acute and prolonged stresses on reproductive function.
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            Confusion and controversy in the stress field.

            H Selye (1975)
            An attempt is made to further clarify present areas of controversy in the stress field, in response to a two-part article by Dr. John W. Mason which concludes in this issue of the Journal of Human Stress. The author tries to elucidate each source of confusion enumerated by Dr. Mason. The continued use of the word "stress" for the nonspecific response to any demand is deemed most desirable. The once vague term can now be applied in a well-defined sense and is accepted in all foreign languages as well, including those in which no such word existed previously in any sense. Subdivision of the stress concept has become necessary as more recent work has led to such notions as "eustress," "distress," "systemic stress" and "local stress." Confusion between stress as both an agent and a result can be avoided only by the distinction between "stress" and "stressor". It is explained that the stress syndrome is--by definition--nonspecific in its causation. However, depending upon conditioning factors, which can selectively influence the reactivity of certain organs, the same stressor can elicit different manifestations in different individuals.
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              Physiology of the circadian timing system: predictive versus reactive homeostasis.

              G. M. Ede (1986)
              Since Cannon first formulated the concept of homeostasis 60 years ago, attention has been focused on the corrective responses initiated after the steady state of the organism is perturbed. In this lecture it is argued that the concept of homeostasis should be extended to include the precisely timed mechanisms of the circadian (and circannual) timing system which enables organisms to predict when environmental challenges are most likely to occur. A mature understanding of homeostasis should encompass both "reactive" responses to changes in physiological variables which have already occurred and the "predictive" responses initiated in anticipation of predictably timed challenges. Such predictive responses have particular value because they enable physiological mechanisms to be utilized immediately, even if they involve a delay of several hours, by activating them at a suitable time in advance of a probable challenge. However, conflicts may often occur between predictions and reality. Examples from sleep-wake behavior, thermoregulation, blood volume homeostasis, and the regulation of potassium balance show that predictive responses often compromise the effectiveness of reactive homeostatic mechanisms even to the point of risking the survival of the organism. It must be concluded that the day-night cycle of the natural environment has played a fundamental role in shaping the evolutionary development of homeostatic mechanisms because of the dominating predictability of diurnal changes in illumination, temperature, food availability, and predator activity.
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                Author and article information

                Journal
                J Circadian Rhythms
                Journal of Circadian Rhythms
                BioMed Central (London )
                1740-3391
                2004
                20 February 2004
                : 2
                : 1
                Affiliations
                [1 ]Departamento de Bioquímica y Biología Molecular III, Facultad de Medicina, Universidad Complutense, Madrid, Spain
                [2 ]Departamento de Fisiología, Facultad de Medicina, Universidad de Buenos Aires, Buenos Aires, Argentina
                Article
                1740-3391-2-1
                10.1186/1740-3391-2-1
                373458
                14977425
                b8f8d46e-5107-4226-8333-d10d23f281f8
                Copyright © 2004 Esquifino et al; licensee BioMed Central Ltd. This is an Open Access article: verbatim copying and redistribution of this article are permitted in all media for any purpose, provided this notice is preserved along with the article's original URL.
                History
                : 24 December 2003
                : 20 February 2004
                Categories
                Research

                Cell biology
                Cell biology

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