Living organisms have been known to spontaneously emit ultraweak photons in
vivo and in vitro. Origin of the photon emission remains unclear, especial
ly in the nervous system. The spontaneous ultraweak photon emission was det
ected here from cultured rat cerebellar granule neurons using a photomultip
lier tube which was highly sensitive to visible light. The photon emission
was facilitated by the membrane depolarization of neurons by a high concent
ration of K+ and was attenuated by application of tetrodotoxin or removal o
f extracellular Ca2+, indicating the photon emission depending on the neuro
nal activity and likely on the cellular metabolism. Furthermore, almost all
the photon emission was arrested by 2,4-dinitrophenylhydrazine, indicating
that the photon emission would be derived from oxidized molecules. Detecti
on of the spontaneous ultraweak photon emission will realize noninvasive an
d real-time monitoring of the redox state of neural tissue corresponding to
the neuronal activity and metabolism. (C) 2001 Academic Press.