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Department of Physiology, Queen's University, Kingston, Ontario, Canada K7L 3N6
Leptin, the
protein product of the
ob/ob
gene, is thought to have a central site of action, presumably within
the hypothalamus, through which it regulates feeding behavior. The
paraventricular nucleus (PVN) is one structure that has been implicated
in regulating feeding behavior. Using patch-clamp recording techniques,
this study examines the direct membrane effects of leptin on neurons in
a coronal PVN slice. Bath application of the physiologically active
leptin fragment (amino acids 22-56) elicited dose-related depolarizations in 82% of the type I cells tested
(n = 17) and 67% of the type II cells
tested (n = 9). By contrast, the
physiologically inactive leptin fragment (amino acids 57-92) had
no discernible effect on membrane potential
(n = 7). The effects of this peptide were unaffected following synaptic isolation of the cells by bath application of the sodium channel blocker tetrodotoxin
(n = 5). Voltage clamp recordings in
six cells demonstrated that leptin increased a nonspecific cation
conductance with a reversal potential near
30 mV. These findings
suggest that neurons in PVN may play an important role in the central
neuronal circuitry involved in the physiological response to leptin.
electrophysiology; feeding; hypothalamus
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