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The effect of salicylates on insulin sensitivity
Mihai G. Netea,1 Cees J. Tack,1 Paetrick M. Netten,2 Jos A. Lutterman,1 and Jos W.M. Van der Meer1
1Department of Medicine, University Medical Center St. Radboud, Nijmegen, The Netherlands2Department of Internal Medicine, Bosch Medicentrum, ‘s-Hertogenbosch, The Netherlands
Address correspondence to: Mihai G. Netea, Department of Medicine (541), University Medical Center St. Radboud, Geert Grooteplein 8, PO Box 9101, 6500 HB Nijmegen, The Netherlands. Phone: 31-24-3614652; Fax: 31-24-3541734; E-mail:M.Netea@aig.azn.nl.
Find articles by Netea, M. in: JCI | PubMed | Google Scholar
1Department of Medicine, University Medical Center St. Radboud, Nijmegen, The Netherlands2Department of Internal Medicine, Bosch Medicentrum, ‘s-Hertogenbosch, The Netherlands
Address correspondence to: Mihai G. Netea, Department of Medicine (541), University Medical Center St. Radboud, Geert Grooteplein 8, PO Box 9101, 6500 HB Nijmegen, The Netherlands. Phone: 31-24-3614652; Fax: 31-24-3541734; E-mail:M.Netea@aig.azn.nl.
Find articles by Tack, C. in: JCI | PubMed | Google Scholar
1Department of Medicine, University Medical Center St. Radboud, Nijmegen, The Netherlands2Department of Internal Medicine, Bosch Medicentrum, ‘s-Hertogenbosch, The Netherlands
Address correspondence to: Mihai G. Netea, Department of Medicine (541), University Medical Center St. Radboud, Geert Grooteplein 8, PO Box 9101, 6500 HB Nijmegen, The Netherlands. Phone: 31-24-3614652; Fax: 31-24-3541734; E-mail:M.Netea@aig.azn.nl.
Find articles by Netten, P. in: JCI | PubMed | Google Scholar
1Department of Medicine, University Medical Center St. Radboud, Nijmegen, The Netherlands2Department of Internal Medicine, Bosch Medicentrum, ‘s-Hertogenbosch, The Netherlands
Address correspondence to: Mihai G. Netea, Department of Medicine (541), University Medical Center St. Radboud, Geert Grooteplein 8, PO Box 9101, 6500 HB Nijmegen, The Netherlands. Phone: 31-24-3614652; Fax: 31-24-3541734; E-mail:M.Netea@aig.azn.nl.
Find articles by Lutterman, J. in: JCI | PubMed | Google Scholar
1Department of Medicine, University Medical Center St. Radboud, Nijmegen, The Netherlands2Department of Internal Medicine, Bosch Medicentrum, ‘s-Hertogenbosch, The Netherlands
Address correspondence to: Mihai G. Netea, Department of Medicine (541), University Medical Center St. Radboud, Geert Grooteplein 8, PO Box 9101, 6500 HB Nijmegen, The Netherlands. Phone: 31-24-3614652; Fax: 31-24-3541734; E-mail:M.Netea@aig.azn.nl.
Find articles by Van der Meer, J. in: JCI | PubMed | Google Scholar
Published December 1, 2001 - More info
J Clin Invest. 2001;108(11):1723–1724. https://doi.org/10.1172/JCI14455.
© 2001 The American Society for Clinical Investigation
Insulin resistance, a characteristic feature of type 2 diabetes, is associated with central obesity, hypertension, dyslipidemia, and cardiovascular disease (and death) (1). The mechanism of insulin resistance is complex and largely unknown. Both in animals and in humans, however, insulin resistance can be induced by lipid infusion. In a recent issue of the JCI, Kim and colleagues presented new data on the mechanisms responsible for the induction of insulin resistance by lipids. In an elegant set of experiments, they show that activation of IKK-β is important in fat-induced insulin (2). High-dose salicylate prevents the fat-induced defects in insulin signaling. Based on these findings, the authors suggest that “salicylates represent a potentially novel class of therapeutic agents for type 2 diabetes” (2).
Although the carefully performed study by Kim et al. provides new insight into the mechanisms of fat-induced insulin resistance, we would like to caution against the preliminary conclusion concerning beneficial effects of salicylates on insulin resistance. First of all, in contrast to the findings of Kim et al. in the triglyceride (TG) infusion model in the rat, earlier studies in human volunteers using hyperglycemic clamp techniques reported increased insulin resistance by salicylate compounds (3, 4). These findings suggest that the effects of salicylates may depend on the experimental model, and possibly on the species studied.
There are also strong theoretical arguments that salicylates have deleterious effects on insulin resistance. Similar to TGs (or fatty acids), the proinflammatory cytokine TNF-α synthesized by adipocytes is a central factor in the pathogenesis of insulin resistance (5). As underlined also by Kim et al., there is significant overlap between the intracellular events induced by fatty acids and TNF in insulin-sensitive tissues: both activate IKK-β and decrease IRS-1 tyrosine phosphorylation, and both increase intracellular ceramide concentrations, which leads to inhibition of Akt/protein kinase B activation and impaired GLUT-4 translocation (these relationships are outlined in Figure 1) (6–8). The effects of salicylates on TNF-induced insulin resistance are completely opposite to those reported by Kim and colleagues on fat-induced insulin resistance. TNF induces the synthesis of prostaglandins (PGs), which function as a negative feedback mechanism by inhibiting the upstream TNF production (9). We and others have shown in healthy volunteers that administration of aspirin or indomethacin, both strong inhibitors of PG synthesis, enhances TNF production capacity at least twofold (10, 11), which can negatively affect insulin sensitivity. In addition, PGs stimulate synthesis of leptin, an adipocytokine known to decrease insulin resistance through improvement of IRS-1−associated phosphatidylinositol (PI) 3-kinase activity (12, 13). Although not yet experimentally tested, inhibition of PG synthesis by salicylate compounds may also negatively influence insulin sensitivity by inhibition of leptin release. Thus, aspirin could increase insulin resistance through at least two mechanisms mediated by the inhibition of PG synthesis, namely the upregulation of TNF synthesis and the inhibition of leptin release (Figure 1). There are other important endogenous factors modulating the resistance to insulin: adiponectin reverses insulin resistance, possibly in part by inhibition of TNF synthesis, whereas resistin impairs glucose tolerance and insulin action (12, 14). The influence of salicylates on the modulation of these proteins is not known.
Figure 1The effects of salicylates on insulin resistance. There is significant overlap between the intracellular events induced by TGs (or FFAs) and TNF regarding the mechanisms of insulin resistance. Both stimuli activate IKK-β and decrease insulin-induced tyrosine phosphorylation of IRS-1; both increase intracellular ceramide concentrations, which leads to inhibition of Akt/protein kinase B activation and inhibition of GLUT-4 translocation. These effects induce a state of insulin resistance. The effects of salicylate compounds on these pathways may be divergent. That is, they may improve insulin resistance by blocking the activation of IKK-β (top), or they may worsen insulin resistance by inhibiting PG synthesis and thus potentiating TNF release (bottom). In addition, inhibition of PG will decrease synthesis of leptin, which is known to improve insulin sensitivity by stimulating IRS-1–associated PI 3-kinase activity. The beneficial effect of leptin on insulin action is thus decreased (bottom).
In conclusion, the influence of salicylate compounds on insulin sensitivity is multifactorial and involves both beneficial and deleterious effects. This should not preclude patients from taking low-dose aspirin to prevent cardiovascular disease (15), but more basal and clinical studies are needed before recommending higher dosages of salicylates for the treatment of type 2 diabetes itself.
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