Differential Responsiveness of Obese (fa/fa) and Lean (Fa/Fa) Zucker Rats to Cytokine‐Induced Anorexia

AbstractPathophysiological and pharmacological concentrations of tumor necrosis factor‐α (TNF‐α) and interleukin‐1β (IL‐1β) in the cerebrospinal fluid (CSF) induce anorexia in normal rats. Obesity in humans and rodents is associated with increased TNF‐α messenger RNA and protein levels in various cell types. This suggests that obese individuals may have differential regulation of cytokine production and dissimilar responsiveness to cytokines. In the present study, we investigated the effects of the intracerebroventricular (ICV) microinfusion of TNF‐α (50, 100, and 500 ng/rat), IL‐1β (1.0, 4.0, and 8.0 ng), and TNF‐α (100 ng) plus IL‐1β (1.0 ng) on obese (fa/fa) and lean (Fa/Fa) Zucker rats. The results show that: TNF‐α and IL‐1β, and the concomitant administration of TNF‐a and IL‐ip decreased the short‐term (4 hours), nighttime (12 hours), and total daily food intakes in obese and lean rats; IL‐1β was more potent relative to TNF‐α; obese rats showed greater responsiveness to IL‐1β: 8.0 ng IL‐1β, for example, decreased the 12‐hour food intake by 52% in obese and 22% in lean rats. On the other hand, obese and lean rats did not exhibit a significantly different responsiveness to the anorexia induced by 50,100, or 500 ng TNF‐α at the 4‐hour period; and the concomitant ICV administration of TNF‐α and IL‐1β induced anorexia with additive (4‐hour period) or synergistic (12‐hour and 24‐hour periods) effects in obese rats. The effect of TNF‐α plus IL‐1β in lean rats was greater than additive for the 12‐hour and 24‐hour periods. The difference in suppression of total daily food intake by TNF‐α plus IL‐1β in obese (‐43%) versus lean (‐23%) rats was significantly different (p<0.01). The results show that obese (fa/fa) and lean (Fa/Fa) Zucker rats have differential responsiveness to the ICV microinfusion of two different classes of cytokines.