Salivary alpha amylase and cortisol responses to different stress tasks: Impact of sex

被引:182
作者
van Stegeren, Anda H. [1 ,2 ]
Wolf, Oliver T. [3 ]
Kindt, Merel [1 ,2 ]
机构
[1] Univ Amsterdam, Dept Clin Psychol, NL-1018 WB Amsterdam, Netherlands
[2] Univ Amsterdam, Cognit Sci Ctr Amsterdam, NL-1018 WB Amsterdam, Netherlands
[3] Ruhr Univ Bochum, Fac Psychol, Dept Cognit Psychol, D-44780 Bochum, Germany
关键词
amylase; cortisol; stress; sex difference; human;
D O I
10.1016/j.ijpsycho.2008.02.008
中图分类号
B84 [心理学];
学科分类号
04 ; 0402 ;
摘要
Neuro-endocrine markers such as salivary alpha amylase (sAA) and cortisol (CORT) play an important role in establishing human responses to stressful events. Whereas sAA levels reflect sympathetic system activity, salivary cortisol appears to be a valid measure for HPA axis activity. Although many studies looked at either sAA or CORT responses in reaction to stress, work still has to be done to look at the way these systems interact, especially when both systems are activated. Additionally, sex effects in CORT responses have been investigated relatively often, but possible sex differences in sAA levels and responses, or the way both systems interact has not been the focus of sufficient studies to yield a univocal conclusion. In this study we presented a group of healthy participants (n = 80) with two mildly stressful tasks, consisting of an aversive Picture rating task and a cold pressor Stress (CPS) task. The second task was compared with a control task. We expected a rise in sAA level in response to the first task and sAA as well as CORT responses on the second task and explored the interaction between the two responses. Results indicate that sAA is indeed a sensitive market in both psychologically and physically induced arousal paradigms, whereas a cortisol response was only observed in the CPS task. Men had higher sAA levels than women during the complete course of the study, but men and women were comparable in their responsivity to the tasks. No strong correlations between sAA and CORT responses were found. (c) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:33 / 40
页数:8
相关论文
共 46 条
[1]   Glucocorticoid release and memory consolidation in men and women [J].
Andreano, JM ;
Cahill, L .
PSYCHOLOGICAL SCIENCE, 2006, 17 (06) :466-470
[2]   Innate secretory immunity in response to laboratory stressors that evoke distinct patterns of cardiac autonomic activity [J].
Bosch, JA ;
De Geus, EJC ;
Veerman, ECI ;
Hoogstraten, J ;
Amerongen, AVN .
PSYCHOSOMATIC MEDICINE, 2003, 65 (02) :245-258
[3]   Psychological stress as a determinant of protein levels and salivary-induced aggregation of Streptococcus gordonii in human whole saliva [J].
Bosch, JA ;
Brand, HS ;
Ligtenberg, TJM ;
Bermond, B ;
Hoogstraten, J ;
Amerongen, AVN .
PSYCHOSOMATIC MEDICINE, 1996, 58 (04) :374-382
[4]   Emotion and Motivation II: Sex Differences in Picture Processing [J].
Bradley, Margaret M. ;
Codispoti, Maurizio ;
Sabatinelli, Dean ;
Lang, Peter J. .
EMOTION, 2001, 1 (03) :300-319
[5]   Impaired memory retrieval correlates with individual differences in cortisol response but not autonomic response [J].
Buchanan, Tony W. ;
Tranel, Daniel ;
Adolphs, Ralph .
LEARNING & MEMORY, 2006, 13 (03) :382-387
[6]   Enhanced human memory consolidation with post-learning stress: Interaction with the degree of arousal at encoding [J].
Cahill, L ;
Gorski, L ;
Le, K .
LEARNING & MEMORY, 2003, 10 (04) :270-274
[7]   Sex-related impairment of memory for emotional events with β-adrenergic blockade [J].
Cahill, L ;
van Stegeren, A .
NEUROBIOLOGY OF LEARNING AND MEMORY, 2003, 79 (01) :81-88
[8]   Sex differences in the neural basis of emotional memories [J].
Canli, T ;
Desmond, JE ;
Zhao, Z ;
Gabrieli, JDE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (16) :10789-10794
[9]   Hormonal responses to psychological stress in men preparing for skydiving [J].
Chatterton, RT ;
Vogelsong, KM ;
Lu, YC ;
Hudgens, GA .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1997, 82 (08) :2503-2509
[10]   Salivary alpha-amylase as a measure of endogenous adrenergic activity [J].
Chatterton, RT ;
Vogelsong, KM ;
Lu, YC ;
Ellman, AB ;
Hudgens, GA .
CLINICAL PHYSIOLOGY, 1996, 16 (04) :433-448