TY - JOUR
T1 - Decreased Cerebrospinal Fluid Allopregnanolone Levels in Women with Posttraumatic Stress Disorder
AU - Rasmusson, Ann M.
AU - Pinna, Graziano
AU - Paliwal, Prashni
AU - Weisman, David
AU - Gottschalk, Christopher
AU - Charney, Dennis
AU - Krystal, John
AU - Guidotti, Alessandro
N1 - Funding Information:
This work was supported by the Veterans Affairs (VA) National Center for PTSD, Clinical Neurosciences Division in West Haven Connecticut, the Yale Women’s Behavioral Health Program, a VA Merit Review (to AMR), National Institute of Mental Health grants MH 49486 and 56890 (to AG), and National Institute on Drug Abuse number 1K12DA14038-01 grant support (to AMR).
PY - 2006/10/1
Y1 - 2006/10/1
N2 - Background: Alterations in the γ-amino-butyric acid (GABA) neurotransmitter system have been identified in some populations with posttraumatic stress disorder (PTSD). Methods: To further investigate factors of relevance to GABAergic neurotransmission in PTSD, we measured cerebrospinal fluid (CSF) levels of allopregnanolone and pregnanolone combined (ALLO: congeners that potently and positively modulate effects of GABA at the GABAA receptor), 5α-dihydroprogesterone (5α-DHP: the immediate precursor for allopregnanolone), dehydroepiandrosterone (DHEA: a negative modulator of GABAA receptor function), and progesterone with gas chromatography, mass spectrometry in premenopausal women with (n = 9) and without (n = 10) PTSD. Subjects were free of psychotropic medications, alcohol, and illicit drugs; all were in the follicular phase of the menstrual cycle except three healthy and four PTSD subjects receiving oral contraceptives. Results: There were no group differences in progesterone, 5α-DHP, or DHEA levels. The PTSD group ALLO levels were < 39% of healthy group levels. The ALLO/DHEA ratio correlated negatively with PTSD re-experiencing symptoms (n = -.82, p < 008; trend) and with Profile of Mood State depression/dejection scores (n = -0.70, p < 0008). Conclusion: Low CSF ALLO levels in premenopausal women with PTSD might contribute to an imbalance in inhibitory versus excitatory neurotransmission, resulting in increased PTSD re-experiencing and depressive symptoms.
AB - Background: Alterations in the γ-amino-butyric acid (GABA) neurotransmitter system have been identified in some populations with posttraumatic stress disorder (PTSD). Methods: To further investigate factors of relevance to GABAergic neurotransmission in PTSD, we measured cerebrospinal fluid (CSF) levels of allopregnanolone and pregnanolone combined (ALLO: congeners that potently and positively modulate effects of GABA at the GABAA receptor), 5α-dihydroprogesterone (5α-DHP: the immediate precursor for allopregnanolone), dehydroepiandrosterone (DHEA: a negative modulator of GABAA receptor function), and progesterone with gas chromatography, mass spectrometry in premenopausal women with (n = 9) and without (n = 10) PTSD. Subjects were free of psychotropic medications, alcohol, and illicit drugs; all were in the follicular phase of the menstrual cycle except three healthy and four PTSD subjects receiving oral contraceptives. Results: There were no group differences in progesterone, 5α-DHP, or DHEA levels. The PTSD group ALLO levels were < 39% of healthy group levels. The ALLO/DHEA ratio correlated negatively with PTSD re-experiencing symptoms (n = -.82, p < 008; trend) and with Profile of Mood State depression/dejection scores (n = -0.70, p < 0008). Conclusion: Low CSF ALLO levels in premenopausal women with PTSD might contribute to an imbalance in inhibitory versus excitatory neurotransmission, resulting in increased PTSD re-experiencing and depressive symptoms.
KW - GABA
KW - Posttraumatic stress disorder
KW - allopregnanolone
KW - dehydroepiandrosterone
KW - depression
KW - women
UR - http://www.scopus.com/inward/record.url?scp=33748901641&partnerID=8YFLogxK
U2 - 10.1016/j.biopsych.2006.03.026
DO - 10.1016/j.biopsych.2006.03.026
M3 - Article
C2 - 16934764
AN - SCOPUS:33748901641
SN - 0006-3223
VL - 60
SP - 704
EP - 713
JO - Biological Psychiatry
JF - Biological Psychiatry
IS - 7
ER -