KATch-UP Mondays: Men Handle Stress BETTER Than Women? Hmmm …

It is obvious that male and female roles are different. No doubt about that. It’s safer to say that both genders handle stress equally than to say one or the other, but researchers have a different opinion.

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Gender differences in stress response: Role of developmental and biological determinants

Rohit VermaYatan Pal Singh Balhara,1 and Chandra Shekhar Gupta2Author informationCopyright and License informationDisclaimer This article has been cited by other articles in PMC.Go to:


Stress response is associated with manifestations of various psychosomatic and psychiatric disorders. Hence, it is important to understand the underlying mechanisms that influence this association. Moreover, men and women tend to react differently with stress–both psychologically and biologically. These differences also need to be studied in order to have a better understanding in the gender difference observed for many disorders, which are likely to be contributed by the gender difference in stress reactivity and responses. Such an understanding would have a significant impact on our understanding about how adult health is set during early life and how adult disease could be prevented in men and women. Keywords: Gender, psychiatric disorders, stress response

Stress can be defined as a real or interpreted threat to the physiological or psychological integrity of an individual that results in physiological and behavioral responses. In Eastern cultures, stress has been viewed as an absence of inner peace. On the other hand, the Western culture has viewed stress as a loss of control.

Gender is an important determinant of human health, and there is a clear pattern for the sex-specific prevalence rates of various mental and physical disorders. Susceptibility to infectious diseases, hypertension, aggressive behavior, and drug abuse is generally observed to be higher in men. Conditions such as autoimmune diseases, chronic pain, depression, and anxiety disorders are relatively more prevalent among women.[14] The observed gender-specific disease pattern may be partly attributed to effects of sex hormones as some of these gender differences emerge during reproductive years and gradually diminish after menopause.[5] Individual differences in stress reactivity have been proposed as a potentially important risk factor for gender-specific health problems in men and women.[2,6]Go to:


Assessment of gender differences in stress reactivity relies primarily on measuring physiological responses to acute stressors in laboratory settings. This includes activities of the Hypothalamic-Pituitary-Adrenal (HPA) axis (eg, cortisol) and sympathetic nervous system (eg, heart rate and blood pressure). Greater acute HPA and autonomic responses have been found in adult men as compared to adult women, with the help of standard performance-related psychosocial stressors such as public speaking.[2,3] Pathogenesis of cardiovascular disease, aggression, and immune suppression in men are likely to be influenced by this greater sympathoadrenal responsiveness.[4,7]

HPA response patterns differ markedly between males and females. This has been demonstrated in both animal and human studies. The biochemical profile of human beings varied from that of rodents with regard to stress-related neurochemicals such as basal Adrenocorticotropic Hormone (ACTH) and corticosterone levels.[8] While the basal level as well as variance in response to stress is uniformly higher in females of rodents, the picture is more complex in humans. A relatively higher secretion of ACTH with comparable total cortisol levels under basal conditions has been observed in men. This finding reflects an increased sensitivity of the adrenal cortex in women as compared to men.[9] However, no gender differences are observed at the pituitary level on challenging with synthetic Human Corticotropin-Releasing Factor (h-CRF) with or without pretreatment with dexamethasone.[10,11] The response is different to ovine CRF[12] or a combination of h-CRF and vasopressin with respect to ACTH secretion, with women being more responsive.[11]Go to:


Female sex hormones attenuate the sympathoadrenal and HPA responsiveness. This leads to sluggish cortisol feedback on the brain and less or delayed containment of the stress response. Tendency of women to develop depression is related to the compromised cortisol feedback effects on HPA arousal.[2,6] Ovariectomy leads to attenuated HPA responses, whereas estradiol substitution induces HPA stimulation in animal studies.[13] An increased HPA-axis response to stress in females is observed in gonadectomized or neonatally estrogenized rats. This effect is independent of differences in circulating gonadal steroid levels.[14] This suggests an innate or organized difference in the HPA-axis response to stress. Genomic differences, organizationally or developmentally programmed effects (caused by earlier differential gonadal steroid exposure), and/or acute, activational effects of recent gonadal steroid exposure are some of the possible underlying mechanisms reflected in the observed sex differences in the central nervous system function. The sex differences in HPA axis responses would be expected to disappear if gonadal steroids were removed. On the contrary, sexual dimorphism would persist if the responses were not dependent on the concurrent gonadal steroids. Low levels of estradiol are observed in the early follicular phase, which peak shortly before or during ovulation and slowly decrease throughout the luteal phase. Basal as well as stimulated ACTH and corticosterone levels are the highest around the time of ovulation in rats.[15] Human studies have produced inconsistent results with respect to possible changes in the HPA activity during the menstrual cycle.[16]Go to:


There is a difference in susceptibility of women and men to specific immunological disorders. This suggests gender dimorphism of the immune system. Gender may exert differential effects on the immune system by modulating Glucocorticoid (GC) sensitivity of proinflammatory cytokine production.[17] The HPA axis can be activated by a wide variety of psychosocial and physiological stressors. This results in the secretion of GCs and modulation of specific immune responses. Psychosocial stress, such as academic examinations, leads to decreased cellular immune function.[18] This is mediated by profound changes in cytokine secretion. GCs suppress major type 1 cytokines, interferon-alpha, and Interleukin (IL)-2, produced by TH1 helper cells. However, type 2 cytokines, IL-4, and IL-10 remain unchanged. Humoral immune responses are favoured, while cell-mediated immunity is suppressed by this shift toward a type 2 cytokine pattern.[19] GCs specifically inhibit the production of proinflammatory cytokines (IL-6, IL-1, and Tumor Necrosis Factor (TNF)-alpha) in monocytes and macrophages. The anti-inflammatory cytokines remain unaffected or are even stimulated.[20]

HPG axis exerts direct and indirect effects on the immune system. HPA axis acts as a regulatory feedback loop that shuts off inflammatory responses to invading antigens after the initial response or in a state of stress. Cellular immunity is inhibited by estrogen, as it induces a shift in cytokine balance toward a type 2 cytokine response.[21] Monocytes and macrophages are affected in a dose-dependent manner. Inhibition of proinflammatory cytokine production occurs at higher concentrations and stimulation at lower concentrations.[22] Proinflammatory cytokine production is inhibited by progesterone as well. This action of progesterone is mediated by its competitive binding to the GC receptor.[23] Testosterone inhibits immune functions to some extent.[21,24]Go to:

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The understanding of neuroanatomical substrates underlying human emotional processes tightly related to stress has been facilitated by functional neuroimaging studies.[25,26] However, these studies suffer from a major limitation. The majority of emotional stimuli employed in existing Functional Magnetic Resonance Imaging (fMRI) studies (eg, fearful faces) lack critical features of a standard psychosocial stress paradigm. Such a paradigm comprises motivated performance tasks along with social-evaluative threat and/or subjective feelings of uncontrollability.[27] A gender-specific neural activation model underlying the central stress response has been observed in these studies. This includes asymmetric prefrontal activity in males and, primarily, limbic activation in females.[28]

Negative affective style and suppressed immune function have been associated with high levels of right-sided prefrontal activation.[29] The Right Parieto-Frontal Cortex (RPFC) plays a major role in regulating negative emotions. This effect is most evident in moderating and inhibiting Dorsal Anterior Cingulate Cortex (DACC) and amygdala hyperactivities associated with negative affect.[30,31]

Persistent DACC activation following stress observed in female subjects might predispose women to mood disorders and depression if there is no modulating effect of RPFC. RPFC may be a critical neural substrate mediating adaptation and coping under stress.[32] Activation of RPFC and right parietal regions has been associated with various cognitive control tasks, including working memory, response selection, and task switching, as well as inhibitory functions.[33] The role of ventral striatum along with several limbic regions has been implicated in learning, reward, motivation, and emotion.[34] The observed gender differences in central stress responses might be a result of computational roles subserved by these brain regions.

The general trend of greater acute HPA and autonomic responses in males as compared to females by using performance stress paradigms is supported by the neuroimaging findings.[2] A greater degree of emotional “rewinding” (melancholy thinking) or reflection of own emotional traits observed in females as compared to males after completion of stress tasks is a likely consequence of persistent cingulate activation.[35] However, such observations are not consistent across studies. Some studies have found that adoption of social rejection task as the stressor instead of achievement tasks resulted in either no gender difference in stress reactivity or greater cortisol elevation in females.[27] It has been proposed that women are more likely to be negatively affected by interpersonal events than men.[36]

The complex nature of gender-specific stress response is reflected in the differences in experimental findings and alternative theoretical models. The findings are likely to be influenced by type of stressor/challenge, experimental procedure, outcome measured, subject status, and modulation by other stress mediators.[27]Go to:


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The tendency to display negative effect in response to minor stressors in daily life is a part reflection of genetic liability to depression. It has been postulated as a true depression endophenotype.[37,38] However, depressive disorder develops in only a small fraction of individuals exposed to stressful life events (SLEs).[39] This could be result from greater sensitivity to depression-inducing effects of SLEs among some individuals as compared to others.[40,41] Personality trait,[4244] childhood adversity,[45] and indirect measures of genetic risk for depression and anxiety, derived from twin or family studies[46,47] are some of the factors shown to increase sensitivity to SLEs. A length polymorphism in the gene encoding the serotonin transporter (5-HTTLPR) could be responsible for the moderating effect of genetic risk on the relationship between life events and depression.[48] However, this effect was observed only for the mild stressors rather than the severe life events.[49] An interaction between a genetic polymorphism and a stable psychological trait to experience the environment as stressful may be the manifested sign of an underlying interaction between a genetic polymorphism and SLEs.[39] Additionally, the 5-HTTLPR genotype may moderate the association between depressive disorder and the tendency to experience the environment as stressful.

Patients with depression or anxiety tend to score higher on neuroticism, extraversion, and facets of agreeableness and conscientiousness than individuals without these conditions.[50] Neuroticism has been associated with social phobia, agoraphobia, panic disorder, obsessive–compulsive disorder, and major depression. Introversion has been associated with social phobia and agoraphobia. Neuroticism not only predicts the onset of depressive symptoms and depressive disorder,[51] but also increases the risk of exposure to SLEs.[52,53]Go to:


As characterized by Beck, sociotropy reflects a high need for interpersonal relationships with a focus on ‘pleasing others to avoid disapproval’ in order to secure attachments. However, an increased need for independence with an elaborated focus on “control” and personal freedom to reduce possibility of failure is reflected in autonomy.[54] Beck postulates that elevated levels of sociotropy and autonomy increase one’s sensitivity to the depressogenic effects of certain types of stressful life events.

Cognitive styles reflective of ‘concern about disapproval’ and ‘need for control’ pose significant risk for depression independent of the effects of stressful life events.[55] Individuals rating higher on these two cognitive styles are likely to be at greater risk for depression in the presence of stressful life events.[56] Kendler et al. reported that women are more sensitive to depressogenic effects of interpersonal problems with individuals within their proximal network.[57] Ruminative thinking is also more common in women and is associated with an increased risk of depression.[58]Go to:

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There is a difference in the stress response exhibited by men and women. It is characterized by ‘fight-or-flight’ in men and ‘tend-and-befriend’ in women.[59] This hypothesis is supported by neuroendocrine and behavioral evidence. The physiological stress response typically involves activation of the sympathetic nervous system and the HPA axis in both genders. However, the stress response specifically builds on attachment care-giving processes in females. This tends to buffer the sympathetic and HPA arousal.

It was observed that the RPFC is activated and Left Orbitofrontal Cortex (LOrF) is suppressed by stress. RPFC is an important part of both the negative emotion and vigilance systems and LOrF is associated with positive emotion and hedonic goals.[60] The hypothesis that stress responses in men may be primarily characterized as “fight-or-flight” is supported by the observation that RPFC activation and LOrF deactivation with stress is predominately observed in the male brain. Involvement of the limbic system including ventral striatum, putamen, insula, and cingulate cortex underlies the stress response in females.[61] The observed limbic activation to stress in female subjects is more consistent with a ‘tend-and-befriend’ rather than a ‘fight-or-flight’ model.

However, it is noteworthy that ventral striatum activation is not a unique marker for the involvement of the reward system and has been implicated in numerous processes.[62] Also, the isolated fMRI environment is hostile to the formation of social attachment under stress. Some authors have suggested that the gender difference in emotionalism per se may be an ill-posed question.[63,64]

Okay, before I end, I do apologize that the blog got this long. The information just kept getting to me so I decided to share. But I’m excited because I already have another idea for tomorrow’s blog!

Until next time …. don’t stress!

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