Regeneration of olfactory receptor neurons following chemical lesion: time course and enhancement with growth factor administration

C Herzog, T Otto - Brain research, 1999 - Elsevier
C Herzog, T Otto
Brain research, 1999Elsevier
Although it has been known for over 50 years that olfactory receptor neuron (ORN)
neurogenesis and subsequent reinnervation of the olfactory bulb (OB) occurs following ORN
injury, the precise intrinsic and extrinsic factors that regulate this dynamic process have not
yet been fully identified. In the first of two experiments, we characterized the time course of
anatomical recovery following zinc sulfate (ZnSO4) lesion of ORNs in adult male Sprague–
Dawley rats. ZnSO4 produced a near complete deafferentation of OB within 3 days following …
Although it has been known for over 50 years that olfactory receptor neuron (ORN) neurogenesis and subsequent reinnervation of the olfactory bulb (OB) occurs following ORN injury, the precise intrinsic and extrinsic factors that regulate this dynamic process have not yet been fully identified. In the first of two experiments, we characterized the time course of anatomical recovery following zinc sulfate (ZnSO4) lesion of ORNs in adult male Sprague–Dawley rats. ZnSO4 produced a near complete deafferentation of OB within 3 days following intranasal administration. A time-dependent increase in ORN reinnervation of OB was observed following 10, 20, and 30 day recovery intervals. Given the evidence that bFGF, EGF, and TGF-α have mitogenic effects on ORNs in vitro, a second experiment examined the extent to which these growth factors (GFs) might enhance ORN regeneration and subsequent reinnervation of OB in vivo. Rats received intranasal infusions of ZnSO4 on day 0, followed by subcutaneous injections of either bFGF (5, 10, or 50 μg/kg), EGF (5, 10, or 50 μg/kg), or TGF-α (5 or 10 μg/kg) on days 3–6. Horseradish peroxidase (HRP) histochemistry of OB following a 10-day recovery period revealed a dose-related enhancement in reinnervation of OB for each of the three growth factors examined, with the greatest enhancement produced by TGF-α. These data suggest that GFs may regulate ORN mitogenesis in vivo in a way similar to that which has been characterized in vitro.
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