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Review

TRP Channels in the Brain: What Are They There For?

In: Neurobiology of TRP Channels. Boca Raton (FL): CRC Press/Taylor & Francis; 2017. Chapter 16.
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Review

TRP Channels in the Brain: What Are They There For?

Seishiro Sawamura et al.
Free Books & Documents

Excerpt

Transient receptor potential (TRP) family proteins form tetrameric nonselective cation channels. Upon activation, TRP channels depolarize the membrane potential, which can lead to activation or inactivation of voltage-gated ion channels, and regulate Ca2+ signaling, which controls diverse cellular functions (Wu et al., 2010; Nilius and Szallasi, 2014). It is well known that some members of the TRP canonical (TRPC), TRP melastatin (TRPM), and TRP vanilloid (TRPV) subfamilies of TRP channels are highly expressed and play important roles in the brain (Vennekens et al., 2012; Nilius and Szallasi, 2014). They regulate diverse neuronal and glial functions including developmental and homeostatic functions of the brain. Recent studies show that dysregulation of the TRP channel functions is involved in various pathological events of neurological and psychiatric disorders. Here, we review the current insights of the physiological roles of the TRPC, TRPM, and TRPV channels, mainly TRPC3/TRPC6/TRPC7, TRPM2, and TRPV1 in neurons and glia, and their pathophysiological roles in neurological and psychiatric disorders.

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References

    1. Abramowitz, J. and Birnbaumer L.. 2009. Physiology and pathophysiology of canonical transient receptor potential channels. FASEB J, 23(2): 297–328. - PMC - PubMed
    1. Aguiar, D.C., et al. 2009. Anxiolytic-like effects induced by blockade of transient receptor potential vanilloid type 1 (TRPV1) channels in the medial prefrontal cortex of rats. Psychopharmacology, 205(2): 217–225. - PubMed
    1. Akita, T. and Okada Y.. 2011. Regulation of bradykinin-induced activation of volume-sensitive outwardly rectifying anion channels by Ca2+ nanodomains in mouse astrocytes. J Physiol, 589(Pt 16): 3909–3927. - PMC - PubMed
    1. Alim, I., et al. 2013. Modulation of NMDAR subunit expression by TRPM2 channels regulates neuronal vulnerability to ischemic cell death. J Neurosci, 33(44): 17264–17277. - PMC - PubMed
    1. Amaral, M.D. and Pozzo-Miller L.. 2007. TRPC3 channels are necessary for brain-derived neurotrophic factor to activate a nonselective cationic current and to induce dendritic spine formation. J Neurosci, 27(19): 5179–5189. - PMC - PubMed

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