8 results on '"Dhabhar, F S"'
Search Results
2. Resting leukocyte telomerase activity is elevated in major depression and predicts treatment response
- Author
-
Wolkowitz, O M, primary, Mellon, S H, additional, Epel, E S, additional, Lin, J, additional, Reus, V I, additional, Rosser, R, additional, Burke, H, additional, Compagnone, M, additional, Nelson, J C, additional, Dhabhar, F S, additional, and Blackburn, E H, additional
- Published
- 2011
- Full Text
- View/download PDF
3. A hassle a day may keep the pathogens away: The fight-or-flight stress response and the augmentation of immune function
- Author
-
Dhabhar, F. S., primary
- Published
- 2009
- Full Text
- View/download PDF
4. A Hassle a Day May Keep the Doctor Away: Stress and the Augmentation of Immune Function
- Author
-
Dhabhar, F. S., primary
- Published
- 2002
- Full Text
- View/download PDF
5. Stress-induced changes in skin barrier function in healthy women.
- Author
-
Altemus M, Rao B, Dhabhar FS, Ding W, and Granstein RD
- Subjects
- Adolescent, Adrenocorticotropic Hormone blood, Adult, Epinephrine blood, Exercise, Female, Humans, Hydrocortisone blood, Interleukin-1 blood, Interleukin-10 blood, Interviews as Topic, Killer Cells, Natural cytology, Killer Cells, Natural immunology, Norepinephrine blood, Sleep Deprivation immunology, Sleep Deprivation physiopathology, Tumor Necrosis Factor-alpha metabolism, beta-Endorphin blood, Skin Physiological Phenomena immunology, Stress, Psychological immunology, Stress, Psychological physiopathology
- Abstract
Despite clear exacerbation of several skin disorders by stress, the effect of psychologic or exertional stress on human skin has not been well studied. We investigated the effect of three different stressors, psychologic interview stress, sleep deprivation, and exercise, on several dermatologic measures: transepidermal water loss, recovery of skin barrier function after tape stripping, and stratum corneum water content (skin conductance). We simultaneously measured the effects of stress on plasma levels of several stress-response hormones and cytokines, natural killer cell activity, and absolute numbers of peripheral blood leukocytes. Twenty-five women participated in a laboratory psychologic interview stress, 11 women participated in one night of sleep deprivation, and 10 women participated in a 3 d exercise protocol. The interview stress caused a delay in the recovery of skin barrier function, as well as increases in plasma cortisol, norepinephrine, interleukin-1beta and interleukin-10, tumor necrosis factor-alpha, and an increase in circulating natural killer cell activity and natural killer cell number. Sleep deprivation also decreased skin barrier function recovery and increased plasma interleukin-1beta, tumor necrosis factor-alpha, and natural killer cell activity. The exercise stress did not affect skin barrier function recovery, but caused an increase in natural killer cell activity and circulating numbers of both cytolytic T lymphocytes and helper T cells. In addition, cytokine responses to the interview stress were inversely correlated with changes in barrier function recovery. These results suggest that acute psychosocial and sleep deprivation stress disrupts skin barrier function homeostasis in women, and that this disruption may be related to stress-induced changes in cytokine secretion.
- Published
- 2001
- Full Text
- View/download PDF
6. Stress-induced enhancement of skin immune function: A role for gamma interferon.
- Author
-
Dhabhar FS, Satoskar AR, Bluethmann H, David JR, and McEwen BS
- Subjects
- Animals, Antigen Presentation physiology, Cell Adhesion Molecules metabolism, Corticosterone blood, Endothelium immunology, Flow Cytometry, Hypersensitivity, Delayed immunology, Immunoglobulin G immunology, Keratinocytes immunology, Leukocytes immunology, Macrophages immunology, Male, Mice, Models, Biological, Time Factors, Interferon-gamma physiology, Skin immunology, Stress, Physiological immunology
- Abstract
Contrary to the widespread belief that stress is necessarily immunosuppressive, recent studies have shown that, under certain conditions, stress can induce a significant enhancement of a skin cell-mediated immune response [delayed-type hypersensitivity (DTH) or contact hypersensitivity]. Adrenal stress hormones and a stress-induced trafficking of leukocytes from the blood to the skin have been identified as systemic mediators of this immunoenhancement. Because gamma interferon (IFNgamma) is an important cytokine mediator of DTH, the studies described here were designed to examine its role as a local mediator of the stress-induced enhancement of skin DTH. The effect of acute stress on skin DTH was examined in wild-type and IFNgamma receptor-deficient (IFNgammaR-/-) mice that had previously been sensitized with 2,4-dinitro-1-fluorobenzene. Acutely stressed wild-type mice showed a significantly larger DTH response than nonstressed mice. In contrast, IFNgammaR-/- mice failed to show a stress-induced enhancement of skin DTH. Immunoneutralization of IFNgamma in wild-type mice significantly reduced the stress-induced enhancement of skin DTH. In addition, an inflammatory response induced by direct IFNgamma administration to the skin was significantly enhanced by acute stress. Our results suggest that IFNgamma is an important local mediator of a stress-induced enhancement of skin DTH. These studies are clinically relevant because, depending on the nature of the antigen, DTH reactions mediate numerous protective (e.g., resistance to viral, bacterial, parasitic, and fungal infections) or pathological (e.g., autoimmune reactions and contact sensitivity reactions such as that to poison ivy) immune responses.
- Published
- 2000
- Full Text
- View/download PDF
7. Enhancing versus suppressive effects of stress hormones on skin immune function.
- Author
-
Dhabhar FS and McEwen BS
- Subjects
- Animals, Corticosterone physiology, Dinitrofluorobenzene, Immunity, Cellular, Lymph Nodes immunology, Male, Oxazolone, Rats, Rats, Sprague-Dawley, Restraint, Physical, Skin drug effects, Time Factors, Adrenalectomy, Corticosterone pharmacology, Dermatitis, Allergic Contact immunology, Dexamethasone pharmacology, Epinephrine pharmacology, Skin immunology, Stress, Psychological immunology, T-Lymphocytes immunology
- Abstract
Delayed-type hypersensitivity (DTH) reactions are antigen-specific cell-mediated immune responses that, depending on the antigen, mediate beneficial (e.g., resistance to viruses, bacteria, and fungi) or harmful (e.g., allergic dermatitis and autoimmunity) aspects of immune function. Contrary to the idea that stress suppresses immunity, we have reported that short-duration stressors significantly enhance skin DTH and that a stress-induced trafficking of leukocytes to the skin may mediate this immunoenhancement. Here, we identify the hormonal mediators of a stress-induced enhancement of skin immunity. Adrenalectomy, which eliminates the glucocorticoid and epinephrine stress response, eliminated the stress-induced enhancement of skin DTH. Low-dose corticosterone or epinephrine administration significantly enhanced skin DTH and produced a significant increase in the number of T cells in lymph nodes draining the site of the DTH reaction. In contrast, high-dose corticosterone, chronic corticosterone, or low-dose dexamethasone administration significantly suppressed skin DTH. These results suggest a role for adrenal stress hormones as endogenous immunoenhancing agents. These results also show that hormones released during an acute stress response may help prepare the immune system for potential challenges (e.g., wounding or infection) for which stress perception by the brain may serve as an early warning signal.
- Published
- 1999
- Full Text
- View/download PDF
8. MIF expression in the rat brain: implications for neuronal function.
- Author
-
Bacher M, Meinhardt A, Lan HY, Dhabhar FS, Mu W, Metz CN, Chesney JA, Gemsa D, Donnelly T, Atkins RC, and Bucala R
- Subjects
- Animals, Interleukin-1 genetics, Interleukin-6 genetics, Lipopolysaccharides pharmacology, Macrophage Migration-Inhibitory Factors cerebrospinal fluid, Macrophage Migration-Inhibitory Factors genetics, Macrophages, Male, Monocytes chemistry, RNA, Messenger analysis, Rats, Rats, Sprague-Dawley, Tumor Necrosis Factor-alpha cerebrospinal fluid, Tumor Necrosis Factor-alpha genetics, Brain Chemistry, Macrophage Migration-Inhibitory Factors analysis, Neurons chemistry
- Abstract
Background: The mediator known historically as macrophage migration inhibitory factor (MIF) has been identified recently as being released into the circulation by the anterior pituitary gland as a consequence of stress or during a systemic inflammatory response. Macrophages and T cells also secrete MIF, both in response to proinflammatory factors or upon stimulation with glucocorticoids. Once released, MIF "overrides" or counterregulates the immunosuppressive effects of steroids on cytokine production and immune cellular activation. To further investigate the biology of MIF and its role in the neuroendocrine system, we have studied the regional and cellular expression of MIF in brain tissue obtained from normal rats and rats administered LPS intracisternally., Materials and Methods: Rat brain sections were analyzed by immunohistochemistry utilizing an affinity-purified, anti-MIF antibody raised to recombinant MIF, and by in situ hybridization using a digoxigenin-labeled, antisense MIF cRNA probe. The kinetics of MIF mRNA expression in brain were compared with that of IL-1, IL-6, and TNF-alpha by RT-PCR of total brain RNA. The cerebrospinal fluid content of MIF and TNF-alpha proteins was analyzed by Western blotting and ELISA., Results: A strong baseline expression pattern for MIF was observed in neurons of the cortex, hypothalamus, hippocampus, cerebellum, and pons. By in situ hybridization, MIF mRNA was found predominantly in cell bodies whereas MIF protein was detected mostly within the terminal fields associated with neurons. There was a marked pattern of MIF immunoreactivity within the mossy fibers of the dentate gyrus and dendrites of the hippocampal CA3 field. These structures have been shown previously to be involved in glucocorticoid-induced tissue damage within the hippocampus, suggesting an association between MIF and targets of glucocorticoid action. The intracisternal injection of LPS increased MIF mRNA and protein expression in brain and MIF immunoreactivity was due in part to infiltrating monocytes/macrophages. MIF protein also was found to be rapidly released into the cerebrospinal fluid. This response corresponded with that of LPS-induced cytokine release and MIF mRNA expression increased in a distribution that colocalized in large part with that of TNF-alpha, IL-1 beta, and IL-6., Conclusion: The significant levels of baseline and inducible MIF expression in the brain and its regional association with glucocorticoid action underscore the importance of this mediator as a physiological regulator of the inflammatory stress response and further define its role within the neuroendocrine system.
- Published
- 1998
Catalog
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.