Cerebrospinal fluid levels of the endocannabinoid anandamide are reduced in patients with untreated newly diagnosed temporal lobe epilepsy

被引:65
|
作者
Romigi, Andrea [1 ]
Bari, Monica [3 ]
Placidi, Fabio [1 ]
Marciani, M. Grazia [1 ]
Malaponti, Marilena [2 ]
Torelli, Federico [1 ]
Izzi, Francesca [1 ]
Prosperetti, Chiara [1 ]
Zannino, Silvana [1 ]
Corte, Francesca [1 ]
Chiaramonte, Carlo [4 ]
Maccarrone, Mauro [2 ,5 ]
机构
[1] Univ Roma Tor Vergata, Dipartimento Neurosci, Rome, Italy
[2] Fdn Santa Lucia, CERC, Rome, Italy
[3] Univ Roma Tor Vergata, Dipartimento Med Sperimentale & Sci Biochim, Rome, Italy
[4] Univ Roma La Sapienza, Cattedra Stat Assicurat Roma, Rome, Italy
[5] Univ Teramo, Dipartimento Sci Biomed, Rome, Italy
关键词
Endocannabinoids; Anandamide; 2-Arachidonoylglycerol; Temporal lobe epilepsy; CB1 CANNABINOID RECEPTORS; SYSTEM; HIPPOCAMPUS; EXCITOTOXICITY; MARIJUANA;
D O I
10.1111/j.1528-1167.2009.02334.x
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
P>Purpose: The endocannabinoid system is involved in excitatory/inhibitory balance mechanisms within the central nervous system (CNS). Growing evidence shows that its perturbation leads to development of epileptic seizures in experimental models, thus indicating that endocannabinoids play an intrinsic protective role in suppressing pathologic neuronal excitability. Experimental data also demonstrate that the endocannabinoid anandamide (AEA) can antagonize epileptic discharges in hippocampal tissue. The objective of our study was to measure endocannabinoids levels in the cerebrospinal fluid (CSF) of drug-naive patients affected by temporal lobe epilepsy (TLE). Methods: We measured the levels of both AEA and the other endocannabinoid, 2-arachidonoylglycerol (2-AG), in the CSF of drug-naive patients with TLE. Results: A significant reduction of AEA was found in the CSF of patients with compared with healthy controls (epileptic patients = 2.55 +/- 1.78 pmol/ml; healthy controls = 11.65 +/- 7.53 pmol/ml; n = 9 for both groups, p < 0.01). 2-AG levels, however, were not affected (epileptic patients = 209.5 +/- 146.56; healthy controls = 159.6 +/- 110.2) (n = 6 for both groups, p = 0.48). Discussion: Our findings seem to be consistent with experimental evidence demonstrating a significant prevention of epileptic seizures induced by endocannabinoids in models of epilepsy. Furthermore, they support the hypothesis that AEA may be involved in its pathogenesis, suggesting a hypothetical primary impairment of the endocannabinoid system in untreated TLE. The actual role of this in vivo dysregulation still remains unclear.
引用
收藏
页码:768 / 772
页数:5
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