Low level lindane exposure alters extinction of conditioned fear in rats

被引:6
作者
Cloutier, S [1 ]
Forquer, MR [1 ]
Sorg, BA [1 ]
机构
[1] Washington State Univ, Neurosci Program, Dept Vet & Comparat Anat, Pullman, WA 99164 USA
关键词
extinction; fear conditioning; gamma-1,2,3,4,5,6-hexachlorocyclohexane; limbic; lindane; multiple chemical sensitivity;
D O I
10.1016/j.tox.2005.09.003
中图分类号
R9 [药学];
学科分类号
1007 [药学];
摘要
Gamma-hexachlorocyclohexane (lindane) is a pesticide with the potential to produce long-term effects on fear or anxiety due to its targeting of the GABAA receptor in the brain. Multiple chemical sensitivity (MCS) is a human condition that has been attributed to repeated chemical exposures, with pesticides heavily implicated in the initiation of MCS. The symptoms in MCS patients are wide ranging but prominent among these in a subset of patients is increased evoked panic responses. Drawing a parallel between these responses in MCS patients and a panic model in rats, these studies explored a potential animal model for MCS. The effects of repeated lindane exposure on conditioned fear behavior was examined in adult male Sprague-Dawley rats. Animals were administered vehicle or lindane (intraperitoneally) for either 3 days/week (1, 2 or 5 mg) or 5 days/week (2 mg) over 2 weeks, and 18 days later were examined for anxiety levels on an elevated plus-maze. One day later, animals were trained for fear conditioning to an odor conditioned stimulus (CS). Freezing behavior was measured I day later in the context where pairing occurred, and then for a total of 6 days in a different environment in which either no CS or the CS was presented. After a second 18-day period of no treatment, rats were again tested for their freezing response to the CS for 2 days. Lindane pretreatment did not alter elevated plus-maze performance, nor did it alter contextual freezing behavior. However, pretreatment with lindane decreased the extinction of fear conditioning to the CS such that freezing behavior in controls was significantly lower than in lindane-pretreated rats, and this effect persisted during testing 18 days later. The results indicate that repeated low-level lindane exposure may produce long-lasting changes in anxiety-related neural circuitry. This suggests that odor-triggered symptoms associated with an aversive event may persist in MCS patients because of the ability of some chemicals to alter fear or anxiety circuitry in the brain. (c) 2005 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:147 / 154
页数:8
相关论文
共 31 条
[1]
Ashford N., 1998, Chemical exposures: low levels and high stakes
[2]
Idiopathic environmental intolerance: Increased prevalence of panic disorder-associated cholecystokinin B receptor allele 7 [J].
Binkley, K ;
King, N ;
Poonai, N ;
Seeman, P ;
Ulpian, C ;
Kennedy, J .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2001, 107 (05) :887-890
[3]
Panic response to sodium lactate infusion in patients with multiple chemical sensitivity syndrome [J].
Binkley, KE ;
Kutcher, S .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1997, 99 (04) :570-574
[4]
COMPARISON OF PATIENTS WITH CHRONIC FATIGUE SYNDROME, FIBROMYALGIA, AND MULTIPLE CHEMICAL SENSITIVITIES [J].
BUCHWALD, D ;
GARRITY, D .
ARCHIVES OF INTERNAL MEDICINE, 1994, 154 (18) :2049-2053
[5]
Anxiety sensitivity and depression in multiple chemical sensitivities and asthma [J].
Caccappolo-van Vliet, E ;
Kelly-McNeil, K ;
Natelson, B ;
Kipen, H ;
Fiedler, N .
JOURNAL OF OCCUPATIONAL AND ENVIRONMENTAL MEDICINE, 2002, 44 (10) :890-901
[6]
A review of a two-phase population study of multiple chemical sensitivities [J].
Caress, SM ;
Steinemann, AC .
ENVIRONMENTAL HEALTH PERSPECTIVES, 2003, 111 (12) :1490-1497
[7]
COMPARATIVE ACCELERATION OF LINDANE METABOLISM TO CHLOROPHENOLS BY PRETREATMENT OF RATS WITH LINDANE OR WITH DDT AND LINDANE [J].
CHADWICK, RW ;
FREAL, JJ .
FOOD AND COSMETICS TOXICOLOGY, 1972, 10 (06) :789-&
[8]
Davis M, 1997, J NEUROPSYCH CLIN N, V9, P382
[9]
SEIZURE THRESHOLDS IN KINDLED ANIMALS ARE REDUCED BY THE PESTICIDES LINDANE AND ENDOSULFAN [J].
GILBERT, ME ;
MACK, CM .
NEUROTOXICOLOGY AND TERATOLOGY, 1995, 17 (02) :143-150
[10]
Gilbert ME, 2001, ANN NY ACAD SCI, V933, P68