Brain Metabolism

Keywords

1. Astrocyte Function in CNS
2. BK Channels in Neuroprotection
3. Heme Oxygenase in Brain Disease
4. Antioxidants in Neurodegeneration
5. Glial Cells and Brain Metabolism

Astrocytes: Guardians and Engineers of the Brain’s Microenvironment

Astrocytes, the star-shaped glial cells of the central nervous system (CNS), are emerging as pivotal players in brain health and disease. Long overshadowed by neurons in CNS research, astrocytes are gaining recognition not just for their support roles, but also as dynamic entities shaping neural function. Their myriad roles encompass homeostasis of neurotransmitters like glutamate, modulation of ion fluxes, such as calcium (Ca^2+), and the release of protective metabolites – the symphony directing the CNS orchestra. Of particular interest is the function of the large-conductance Ca^2+-activated K^+ (BK) channels and the heme oxygenase (HO) system in astrocytes.

Beyond Support: Astrocytes as Active CNS Participants

Astrocytes outnumber neurons in the human brain and engage in critical regulatory activities within the CNS (Kim Yonghee et al., 2019). They balance neurotransmitter levels, particularly glutamate, by uptake and release, preventing excitotoxicity. Furthermore, astrocytes manage ion homeostasis, including Ca^2+ signaling, essential for various physiological processes (Abbott et al., 2006).

BK Channels: The Keys to Cellular Excitability & Protection

BK channels, expressed in astrocytes, are integrally linked to the function of these glial cells (Contet et al., 2016). These channels, activated by Ca^2+, contribute to setting membrane potentials and regulating intracellular signaling. They allow rapid outflow of K^+ during elevated intracellular Ca^2+, linking cellular metabolism to electrical signaling. In astrocytes, BK channel activity has been associated with vascular tone regulation in the brain, demonstrating their vital role in cerebral blood flow and thus, in neurovascular coupling (Gribkoff et al., 2001).

Heme Oxygenase System: A Shield Against Oxidative Assault

The heme oxygenase (HO) system, including its metabolic products such as carbon monoxide (CO), plays a critical antioxidative and cytoprotective role. The activity of HO in the brain modulates inflammatory responses, neuronal survival, and may be influential in the adaptive response of astrocytes to stress (Choi et al., 2017). HO metabolites have been implicated in protective pathways against oxidative stress, offering promise as a therapeutic target in CNS diseases associated with oxidative damage (Hettiarachchi et al., 2017).

Astrocytes in CNS Pathologies: The Double-Edged Sword

The beneficial contributions of BK channels and HO in astrocytes, however, do come with a caveat. In the context of CNS pathologies such as Alzheimer’s disease (AD), these mechanisms can become dysregulated. Reactive astrocytes, a form of astrocyte activation in response to CNS injury or disease, have been shown to induce both protective and deleterious effects, complicating the pathophysiological landscape of neurodegenerative conditions (Liddelow et al., 2017).

BK Channels and HO in Neurodegenerative Diseases

Research indicates that BK channel dysfunction in astrocytes is linked to various CNS disorders (Seifert et al., 2018). In AD, BK channels have shown involvement in amyloid-beta clearance, potentially influencing the progression of the disease (Zhang et al., 2018). Similarly, the HO pathway in astrocytes contributes significantly to the cellular reaction to neurodegenerative processes. Modulation of heme oxygenase activity has been associated with responses to amyloid-beta toxicity, suggesting its role in the pathogenesis of conditions like AD (Chen-Roetling et al., 2005).

Emerging Therapeutic Horizons: Astrocyte-Targeted Interventions

The dual functions of astrocytes, influenced by BK channels and HO metabolites, offer a promising avenue for therapeutic development. Harnessing the protective aspects of these pathways while mitigating potential harmful responses could lead to novel treatments for CNS disorders. Research is ongoing to understand the intricate balance required to utilize astrocytes’ capabilities for CNS repair and neuroprotection.

Conclusion: Envisioning a Brighter Future in CNS Healthcare

The study on astrocytes, particularly the role of BK channels and HO metabolites, marks a significant leap in understanding CNS physiology and pathology. It opens up pathways towards developing treatments that could potentially alleviate, if not reverse, the effects of devastating conditions like AD. As the research community continues to unravel the complexities of astrocytic functions, the future of CNS healthcare inches closer to groundbreaking discoveries and therapies that could change the course of neurodegenerative disease management.

References

1. Kim Yonghee et al. (2019). The Role of Astrocytes in the Central Nervous System Focused on BK Channel and Heme Oxygenase Metabolites: A Review. Antioxidants (Basel), 8(5), 121. doi: 10.3390/antiox8050121
2. Abbott N.J., Ronnback L., Hansson E. (2006). Astrocyte-endothelial interactions at the blood-brain barrier. Nat. Rev. Neurosci., 7, 41-53. doi: 10.1038/nrn1824.
3. Contet C., Goulding S.P., Kuljis D.A., Barth A.L. (2016). BK Channels in the Central Nervous System. Int. Rev. Neurobiol., 128, 281-342.
4. Gribkoff V.K., Starrett Jr J.E., Dworetzky S.I. (2001). Maxi-K potassium channels: form, function, and modulation of a class of endogenous regulators of intracellular calcium. Neuroscientist, 7, 166-177.
5. Chen-Roetling J., Benvenisti-Zarom L., Regan R.F. (2005). Cultured astrocytes from heme oxygenase-1 knockout mice are more vulnerable to heme-mediated oxidative injury. J. Neurosci. Res., 82, 802-810. doi: 10.1002/jnr.20681
6. Liddelow S.A., Guttenplan K.A., Clarke L.E., Bennett F.C., Bohlen C.J., Schirmer L., Bennett M.L., Munch A.E., Chung W.S., Peterson T.C., et al. (2017). Neurotoxic reactive astrocytes are induced by activated microglia. Nature, 541, 481-487. doi: 10.1038/nature21029.
7. Seifert G., Henneberger C., Steinhauser C. (2018). Diversity of astrocyte potassium channels: An update. Brain Res. Bull., 136, 26-36. doi: 10.1016/j.brainresbull.2016.12.002.
8. Zhang F.X., Gadotti V.M., Souza I.A., Chen L., Zamponi G.W. (2018). BK Potassium Channels Suppress Cavalα2δ Subunit Function to Reduce Inflammatory and Neuropathic Pain. Cell Rep., 22, 1956-1964. doi: 10.1016/j.celrep.2018.01.073.
9. Choi Y.K., Kim J.H., Lee D.K., Lee K.S., Won M.H., Jeoung D., Lee H., Ha K.S., Kwon Y.G., Kim Y.M. (2017). Carbon Monoxide Potentiation of L-Type Ca2+ Channel Activity Increases HIF-1alpha-Independent VEGF Expression via an AMPKalpha/SIRT1-Mediated PGC-1alpha/ERRalpha Axis. Antioxid. Redox Signal., 27, 21-36. doi: 10.1089/ars.2016.6684.