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Enkephalin-like immunoreactivity in the chick brainstem: possible relation to the cochlear efferent system
Hearing Research
|July 1, 1995
Summary
In chickens, enkephalin-like immunoreactivity (Enk-LI) is not found in cochlear efferent neurons. However, Enk-LI terminals are densely located near these neurons in the auditory brainstem.
Area of Science:
- Neuroscience
- Auditory System Research
- Neuroanatomy
Background:
- Mammalian lateral olivocochlear (LOC) neurons expressing choline acetyltransferase (ChAT) also show enkephalin (Enk) immunoreactivity.
- The presence of Enk-like immunoreactivity (Enk-LI) in avian cochlear efferent neurons remains uncharacterized.
Purpose of the Study:
- To investigate whether avian cochlear efferent neurons contain Enk-LI.
- To map the distribution of Enk-LI and ChAT-immunoreactive (ChAT-I) neurons and terminals in the domestic chicken's auditory brainstem.
Main Methods:
- Immunohistochemistry was performed on the domestic chicken's auditory brainstem using antisera against ChAT, leucine-enkephalin (L-Enk), and methionine-enkephalin (M-Enk).
- Colchicine injections into the lateral ventricle were used to identify perikarya.
- Distribution of Enk-LI and ChAT-I perikarya and terminals was analyzed.
Main Results:
- Enk-LI terminals were observed around, but not within, the superior olivary nucleus (SO) and nucleus of the lateral lemniscus, pars intermedia (LLi).
- A moderate concentration of Enk-LI terminals was found near the ventrolateral group of ChAT-I cochlear efferent neurons.
- Intensely stained Enk-LI perikarya were located in the nucleus of the lateral lemniscus, pars ventralis (LLv), and scattered in the LLi and nucleus subceruleus ventralis (SCv), with no overlap with ChAT-I somata.
Conclusions:
- In chickens, enkephalin-like immunoreactivity is not present in the somata of cochlear efferent neurons.
- Enkephalinergic terminals are densely concentrated in areas associated with cochlear efferent neurons.
- The nucleus of the lateral lemniscus, pars ventralis (LLv) is a potential source of these enkephalinergic terminals.