Cytokines and Cognition—The Case for A Head‐to‐Toe Inflammatory Paradigm
Abstract
The brain is not only immunologically active of its own accord, but also has complex peripheral immune interactions. Given the central role of cytokines in neuroimmmunoendocrine processes, it is hypothesized that these molecules influence cognition via diverse mechanisms. Peripheral cytokines penetrate the blood‐brain barrier directly via active transport mechanisms or indirectly via vagal nerve stimulation. Peripheral administration of certain cytokines as biological response modifiers produces adverse cognitive effects in animals and humans. There is abundant evidence that inflammatory mechanisms within the central nervous system (CNS) contribute to cognitive impairment via cytokine‐mediated interactions between neurons and glial cells. Cytokines mediate cellular mechanisms subserving cognition (e.g., cholinergic and dopaminergic pathways) and can modulate neuronal and glial cell function to facilitate neuronal regeneration or neurodegeneration. As such, there is a growing appreciation of the role of cytokine‐mediated inflammatory processes in neurodegenerative diseases such as Alzheimer's disease and vascular dementia. Consistent with their involvement as mediators of bidirectional communication between the CNS and the peripheral immune system, cytokines play a key role in the hypothalamic‐pituitary‐adrenal axis activation seen in stress and depression. In addition, complex cognitive systems such as those that underlie religious beliefs, can modulate the effects of stress on the immune system. Indirect means by which peripheral or central cytokine dysregulation could affect cognition include impaired sleep regulation, micronutrient deficiency induced by appetite suppression, and an array of endocrine interactions. Given the multiple levels at which cytokines are capable of influencing cognition it is plausible that peripheral cytokine dysregulation with advancing age interacts with cognitive aging.
Key Biomarkers
Symptom Clusters
Cited By (6)
- Exaggerated neuroinflammation and sickness behavior in aged mice after activation of the peripheral innate immune systemThe FASEB Journal · 2005
- Cognitive decline and markers of inflammation and hemostasis: the Edinburgh Artery StudyJournal of the American Geriatrics Society · 2007
- Postoperative Impairment of Cognitive Function in RatsAnesthesiology · 2007
- Inflammation and interleukin-1 signaling network contribute to depressive symptoms but not cognitive decline in old ageExperimental Gerontology · 2007
- Neuroinflammation and disruption in working memory in aged mice after acute stimulation of the peripheral innate immune systemBrain Behavior and Immunity · 2008
- Central nervous system inflammation in disease related conditions: mechanistic prospectsBrain Research · 2012
Related Papers
- Herbal Therapeutics for CIRS Biomarkers in Autism Spectrum Disorders: A Mechanistic and Molecular Approach for Neuroimmune Pathology in PediatricsMedical Research Archives · 2025 · 4 shared tags
- Modulation of Sirt1 and FoxO1 on Hypothalamic Leptin‐Mediated Sympathetic Activation and Inflammation in Diet‐Induced Obese RatsJournal of the American Heart Association · 2021 · 4 shared tags
- Leptin as a Potential Modifier of Neuroinflammation: Contrasting Roles in Alzheimer’s Disease and Multiple SclerosisInternational Journal of Molecular Sciences · 2025 · 4 shared tags
- Effects of the combination of intermittent fasting and physical exercise on autophagic and leptin pathway in the hypothalamus of obese mice2022 · 4 shared tags
- The Brain–Skin Axis in Psoriasis—Psychological, Psychiatric, Hormonal, and Dermatological AspectsInternational Journal of Molecular Sciences · 2022 · 4 shared tags
- Oxidative Stress, Plant Natural Antioxidants, and Obesity