Metabolomics in Psychiatric Disorders: What We Learn from Animal Models

被引:27
|
作者
Humer, Elke [1 ]
Probst, Thomas [1 ]
Pieh, Christoph [1 ]
机构
[1] Danube Univ Krems, Dept Psychotherapy & Biopsychosocial Hlth, A-3500 Krems, Austria
关键词
animal models; biomarkers; metabolomics; psychiatric disorders; NATIONAL EPIDEMIOLOGIC SURVEY; GLOBAL BIOCHEMICAL APPROACH; MAJOR DEPRESSIVE DISORDER; PREFRONTAL CORTEX; RAT MODEL; PROTEOMICS ANALYSIS; NUCLEUS-ACCUMBENS; TRAIT ANXIETY; FATTY-ACID; METABOLISM;
D O I
10.3390/metabo10020072
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Biomarkers are a recent research target within biological factors of psychiatric disorders. There is growing evidence for deriving biomarkers within psychiatric disorders in serum or urine samples in humans, however, few studies have investigated this differentiation in brain or cerebral fluid samples in psychiatric disorders. As brain samples from humans are only available at autopsy, animal models are commonly applied to determine the pathogenesis of psychiatric diseases and to test treatment strategies. The aim of this review is to summarize studies on biomarkers in animal models for psychiatric disorders. For depression, anxiety and addiction disorders studies, biomarkers in animal brains are available. Furthermore, several studies have investigated psychiatric medication, e.g., antipsychotics, antidepressants, or mood stabilizers, in animals. The most notable changes in biomarkers in depressed animal models were related to the glutamate-gamma-aminobutyric acid-glutamine-cycle. In anxiety models, alterations in amino acid and energy metabolism (i.e., mitochondrial regulation) were observed. Addicted animals showed several biomarkers according to the induced drugs. In summary, animal models provide some direct insights into the cellular metabolites that are produced during psychiatric processes. In addition, the influence on biomarkers due to short- or long-term medication is a noticeable finding. Further studies should combine representative animal models and human studies on cerebral fluid to improve insight into mental disorders and advance the development of novel treatment strategies.
引用
收藏
页数:20
相关论文
共 50 条
  • [21] What We Can Learn From Animal Behavior
    Lang, Undine E.
    ZEITSCHRIFT FUR PSYCHOLOGIE-JOURNAL OF PSYCHOLOGY, 2015, 223 (03): : 149 - 150
  • [22] What can we learn from animal models of obsessive-compulsive disorder?
    Joel, Daphna
    INTERNATIONAL JOURNAL OF PSYCHOLOGY, 2008, 43 (3-4) : 204 - 204
  • [23] Non-Alcoholic Steatohepatitis: What Can We Learn from Animal Models?
    Almonacid-Urrego, C. C.
    Sanchez-Campos, S.
    Tunon, M. J.
    Gonzalez-Gallego, J.
    CURRENT MEDICINAL CHEMISTRY, 2012, 19 (09) : 1389 - 1404
  • [24] Hippocampal volume decrease in depression: what can we learn from animal models?
    Czeh, B.
    EUROPEAN NEUROPSYCHOPHARMACOLOGY, 2011, 21 : S211 - S212
  • [25] Sex differences in psychiatric disorders: what we can learn from sex chromosome aneuploidies
    Tamar Green
    Shira Flash
    Allan L. Reiss
    Neuropsychopharmacology, 2019, 44 : 9 - 21
  • [26] Sex differences in psychiatric disorders: what we can learn from sex chromosome aneuploidies
    Green, Tamar
    Flash, Shira
    Reiss, Allan L.
    NEUROPSYCHOPHARMACOLOGY, 2019, 44 (01) : 9 - 21
  • [27] The Treatment Prevalence Paradox for Psychiatric Disorders and Their Therapies: What Can We Learn from Practice?
    Voderholzer, Ulrich
    Schramm, Elisabeth
    VERHALTENSTHERAPIE, 2024, 34 (02) : 48 - 50
  • [28] "What a Girl Wants": What Can We Learn From Animal Models of Female Sexual Motivation?
    Guarraci, Fay A.
    Frohardt, Russell J.
    FRONTIERS IN BEHAVIORAL NEUROSCIENCE, 2019, 13
  • [29] Metabolomics in Depression: What We Learn from Preclinical and Clinical Evidences
    Singh, Pooja
    Vasundhara, Boosani
    Das, Nabanita
    Sharma, Ruchika
    Kumar, Anoop
    Datusalia, Ashok Kumar
    MOLECULAR NEUROBIOLOGY, 2025, 62 (01) : 718 - 741
  • [30] WHAT CAN WE LEARN ABOUT RHEUMATOID-ARTHRITIS FROM ANIMAL-MODELS
    KLARESKOG, L
    SPRINGER SEMINARS IN IMMUNOPATHOLOGY, 1989, 11 (03): : 315 - 333