Jockers-Scherübl Maria C, Rentzsch Johannes, Danker-Hopfe Heidi, Radzei Nicole, Schürer Falk, Bahri Sharif, Hellweg Rainer
Department of Psychiatry and Psychotherapy, Charité-University Medicine Berlin, Campus Benjamin Franklin, Eschenallee 3, 14050 Berlin, Germany.
Neurosci Lett. 2006 Jun 12;400(3):262-6. doi: 10.1016/j.neulet.2006.02.056. Epub 2006 Mar 15.
Neurotrophins such as nerve growth factor (NGF) and brain-derived neurotrophic factor (BDNF) are important for the development and maintenance of neuron function. Neurodevelopment is thought to be impaired in schizophrenia, and vulnerable schizophrenic brains may be more sensitive to toxic influences. Thus, cannabis as a neurotoxin (and other substances) may be more harmful to schizophrenic brains than to non-schizophrenic brains, when used chronically. In a previous study we demonstrated an earlier disease onset and significantly higher serum NGF concentrations in drug-naïve schizophrenic patients with previous long-term cannabis abuse than in schizophrenics without cannabis abuse or cannabis abusers without schizophrenia. We therefore investigated whether this difference is still observed after treatment. Serum NGF measured in 114 treated schizophrenic patients (schizophrenia alone, n=66; schizophrenia plus cannabis abuse, n=42; schizophrenia plus multiple substance abuse, n=6) no longer differed significantly among those groups and from the control groups (healthy controls, n=51; cannabis controls, n=24; multiple substance controls, n=6). These results were confirmed by an additional prospective study in 28 patients suffering from schizophrenia (S) or schizophrenia with cannabis abuse (SC). Previously elevated serum NGF levels in the drug-naïve state, also differing between the groups (S: 83.44+/-265.25 pg/ml; SC: 246.89+/-310.24 pg/ml, S versus SC: p=0.03) dropped to 10.72+/-14.13 pg/ml (S) and 34.19+/-38.96 pg/ml (SC) (S versus SC, p>0.05), respectively, after adequate antipsychotic treatment. We thus conclude that antipsychotic treatment leads to recovery of neural integrity, as indicated by renormalized NGF values.
神经营养因子,如神经生长因子(NGF)和脑源性神经营养因子(BDNF),对于神经元功能的发育和维持至关重要。神经发育被认为在精神分裂症中受到损害,而脆弱的精神分裂症大脑可能对毒性影响更为敏感。因此,长期使用时,大麻作为一种神经毒素(以及其他物质)可能对精神分裂症大脑比对非精神分裂症大脑更具危害性。在先前的一项研究中,我们证明,与未滥用大麻的精神分裂症患者或无精神分裂症的大麻滥用者相比,先前长期滥用大麻的未用药精神分裂症患者疾病发作更早,血清NGF浓度显著更高。因此,我们研究了治疗后这种差异是否仍然存在。在114例接受治疗的精神分裂症患者(单纯精神分裂症,n = 66;精神分裂症加大麻滥用,n = 42;精神分裂症加多物质滥用,n = 6)中测量的血清NGF在这些组之间以及与对照组(健康对照,n = 51;大麻对照,n = 24;多物质对照,n = 6)相比不再有显著差异。这些结果在另一项针对28例患有精神分裂症(S)或精神分裂症加大麻滥用(SC)的患者的前瞻性研究中得到了证实。在未用药状态下先前升高的血清NGF水平,在各组之间也存在差异(S:83.44±265.25 pg/ml;SC:246.89±310.24 pg/ml,S与SC相比:p = 0.03),在充分的抗精神病治疗后分别降至10.72±14.13 pg/ml(S)和34.19±38.96 pg/ml(SC)(S与SC相比,p>0.05)。因此,我们得出结论,抗精神病治疗导致神经完整性恢复,这由正常化的NGF值表明。