دورية أكاديمية

Minocycline Abrogates Individual Differences in Nerve Injury-Evoked Affective Disturbances in Male Rats and Prevents Associated Supraspinal Neuroinflammation.

التفاصيل البيبلوغرافية
العنوان: Minocycline Abrogates Individual Differences in Nerve Injury-Evoked Affective Disturbances in Male Rats and Prevents Associated Supraspinal Neuroinflammation.
المؤلفون: O'Brien JA; Brain and Mind Centre, School of Medical Sciences, Faculty of Medicine and Health, The University of Sydney, Sydney, NSW, Australia., Austin PJ; Brain and Mind Centre, School of Medical Sciences, Faculty of Medicine and Health, The University of Sydney, Sydney, NSW, Australia. paul.austin@sydney.edu.au.
المصدر: Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology [J Neuroimmune Pharmacol] 2024 Jun 15; Vol. 19 (1), pp. 30. Date of Electronic Publication: 2024 Jun 15.
نوع المنشور: Journal Article
اللغة: English
بيانات الدورية: Publisher: Springer Science + Business Media Country of Publication: United States NLM ID: 101256586 Publication Model: Electronic Cited Medium: Internet ISSN: 1557-1904 (Electronic) Linking ISSN: 15571890 NLM ISO Abbreviation: J Neuroimmune Pharmacol Subsets: MEDLINE
أسماء مطبوعة: Original Publication: New York, NY : Springer Science + Business Media, c2006-
مواضيع طبية MeSH: Minocycline*/pharmacology , Neuroinflammatory Diseases*/drug therapy, Animals ; Male ; Rats ; Rats, Sprague-Dawley ; Neuralgia/drug therapy ; Neuralgia/metabolism ; Neuralgia/prevention & control ; Hyperalgesia/drug therapy ; Hyperalgesia/prevention & control ; Individuality ; Mood Disorders/drug therapy ; Mood Disorders/etiology ; Peripheral Nerve Injuries/complications
مستخلص: Chronic neuropathic pain precipitates a complex range of affective and behavioural disturbances that differ markedly between individuals. While the reasons for differences in pain-related disability are not well understood, supraspinal neuroimmune interactions are implicated. Minocycline has antidepressant effects in humans and attenuates affective disturbances in rodent models of pain, and acts by reducing neuroinflammation in both the spinal cord and brain. Previous studies, however, tend not to investigate how minocycline modulates individual affective responses to nerve injury, or rely on non-naturalistic behavioural paradigms that fail to capture the complexity of rodent behaviour. We investigated the development and resolution of pain-related affective disturbances in nerve-injured male rats by measuring multiple spontaneous ethological endpoints on a longitudinal naturalistic foraging paradigm, and the effect of chronic oral minocycline administration on these changes. Disrupted foraging behaviours appeared in 22% of nerve-injured rats - termed 'affected' rats - and were present at day 14 but partially resolved by day 21 post-injury. Minocycline completely prevented the emergence of an affected subgroup while only partly attenuating mechanical allodynia, dissociating the relationship between pain and affect. This was associated with a lasting downregulation of ΔFosB expression in ventral hippocampal neurons at day 21 post-injury. Markers of microglia-mediated neuroinflammation were not present by day 21, however proinflammatory microglial polarisation was apparent in the medial prefrontal cortex of affected rats and not in CCI minocycline rats. Individual differences in affective disturbances following nerve injury are therefore temporally related to altered microglial morphology and hippocampal neuronal activation, and are abrogated by minocycline.
(© 2024. The Author(s).)
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فهرسة مساهمة: Keywords: Anhedonia; Chronic constriction injury; Depression-like behaviour; Hippocampus; Pain-related disability; Radial arm maze
المشرفين على المادة: FYY3R43WGO (Minocycline)
تواريخ الأحداث: Date Created: 20240615 Date Completed: 20240615 Latest Revision: 20240618
رمز التحديث: 20240618
مُعرف محوري في PubMed: PMC11180027
DOI: 10.1007/s11481-024-10132-y
PMID: 38878098
قاعدة البيانات: MEDLINE
الوصف
تدمد:1557-1904
DOI:10.1007/s11481-024-10132-y