Interleukin-18 mediates cardiac dysfunction induced by western diet independent of obesity and hyperglycemia in the mouse.

Obesity and diabetes are independent risk factors for heart failure and are associated with the consumption of diet rich in saturated fat and sugar, Western diet (WD), known to induce cardiac dysfunction in the mouse through incompletely characterized inflammatory mechanisms. We hypothesized that the detrimental cardiac effects of WD are mediated by interleukin-18 (IL-18), pro-inflammatory cytokine linked to cardiac dysfunction. C57BL/6J wild-type male mice and IL-18 knockout male mice were fed high-saturated fat and high-sugar diet for 8 weeks. We measured food intake, body weight and fasting glycemia. We assessed left ventricular (LV) systolic and diastolic function by Doppler echocardiography and cardiac catheterization. In wild-type mice, WD induced a significant increase in isovolumetric relaxation time, myocardial performance index and left ventricular end-diastolic pressure, reflecting an impairment in diastolic function, paired with a mild reduction in LV ejection fraction. IL-18 KO mice had higher food intake and greater increase in body weight without significant differences in hyperglycemia. Despite displaying greater obesity, IL-18 knockout mice fed with WD for 8 weeks had preserved cardiac diastolic function and higher left ventricular ejection fraction. IL-18 mediates diet-induced cardiac dysfunction, independent of food intake and obesity, thus highlighting a disconnect between the metabolic and cardiac effects of IL-18.

Introduction

The epidemic in obesity and diabetes has been linked to the consumption of a diet rich in saturated fat and sugars, Western diet (WD), which is by itself able to induce obesity, diabetes, and cardiac systolic and diastolic dysfunction in animals.[1] The molecular mechanisms involved in the diet-induced cardiac dysfunction are largely unknown.

Systemic inflammation negatively affects cardiac function, and predicts exercise capacity and hospital readmission in patients with heart failure.[2, 3] The pro-inflammatory interleukin (IL)-18 is a cytokine of the interleukin-1 family that is abundant in the heart and is involved in the development and progression of cardiac hypertrophy, remodeling and failure.[4, 5] In vitro studies suggest that specific nutrients such as saturated fat and sugars can increase the production of IL-18 through direct activation of the intracellular macromolecular complex Nod-like receptor pyrin domain-containing protein 3 (NLRP3) inflammasome.[6, 7, 8, 9, 10, 11, 12] IL-18, on the other hand, also regulates hunger and satiety, body weight and composition, and glucose metabolism, and it opposes obesity and insulin resistance.[13] IL-18 may therefore represent the missing link between a pro-inflammatory diet, that is, WD, and cardiac dysfunction.[1, 14] In this study, we measured cardiac and systemic effects of WD in mice with IL-18 genetic deletion (IL-18 KO) testing two competing hypotheses, one by which deletion of IL-18 would promote greater food intake and weight gain, thus enhancing the negative impact of WD on cardiac function, and the alternative hypothesis by which deletion of IL-18 will protect the heart from the negative effects of WD, thus preserving cardiac function.

Materials and methods

Experiments were conducted in 8- to 10-week old male genetically modified mice lacking the gene for IL-18 (IL-18 knockout (KO) mice) (Jackson Laboratories, Bar Harbor, ME, USA) and age-matched C57BL/6J wild-type (WT) male mice (Envigo, Madison, WI, USA). A group of age-matched male CD1 WT mice (Envigo) was used to measure IL-18 mRNA in the heart (real-time PCR, SYBR Green PCR master mix; Life Technologies, Carlsbad, CA, USA) and IL-18 serum levels (ELISA, Quant; Bio-Tek, Winooski, VT, USA) after 8 weeks of WD (TD.88137; Envigo) compared with Standard diet (Teklad LM-485; Envigo).

We fed IL-18 KO and WT mice with WD (TD.88137; Envigo) providing unlimited access to food.[1] Food intake was measured daily, body weight weekly. Capillary glucose was obtained from the tail at baseline and 8 weeks (Clarity Diagnostics, Boca Raton, FL, USA), after 8–10 h fasting.

Mice underwent transthoracic Doppler echocardiography (Vevo770; VisualSonics, Toronto, ON, Canada) under sedation (30–50 mg kg−1 pentobarbital) at baseline, 4 and 8 weeks.[1] Left ventricular (LV) catheterization with a retrograde right carotid artery approach (Millar Inc., Houston, TX, USA) to measure LV end-diastolic pressure (LVEDP) was performed at 8 weeks under anesthesia (50–70 mg kg−1 pentobarbital), prior to killing.[1] The hearts were explanted to measure LV interstitial fibrosis using Masson's trichrome (Sigma-Aldrich, St Louis, MO, USA) computer morphometric analysis (Image ProPlus 6.0 software, Media Cybernetics, Rockville, MD, USA).[1] Values were expressed as the mean and standard error of the mean. The statistical analysis was performed using SPSS 22.0 (IBM Corp., Armonk, NY, USA). Differences within each group or between groups were analyzed using the Student's T-test for paired and unpaired data, respectively. A sample size of 6 or more for each group provided a power >80% (α=0.05) to detect a meaningful difference defined as difference between means exceeding the standard deviation in each group. No animals or samples were excluded from the data analysis. The investigators performing echocardiography or samples analyses were blinded to the treatment allocations and genotype of the animals. The investigator feeding and handling mice kept other investigators blinded to the treatment and the genotype. No randomization was performed. All studies were approved by the Virginia Commonwealth University Institutional Animal Care and Use Committee and conducted according to the NIH guidelines.

Results

Compared with mice fed standard diet, WD significantly increased IL-18 plasma levels (+35%, P=0.01) and IL-18 cardiac mRNA expression (+127%, P=0.04) (Supplementary Figure S1). There were no significant differences in cardiac or metabolic parameters between IL-18 KO and WT mice at baseline (Supplementary Figure S2). IL-18 KO mice on WD had a higher 8-week cumulative caloric intake (804±2 vs 765±10 kcal, P<0.001; Figure 1a) and weight gain (+38.8% vs +20.0%, P<0.001; Figure 1b), without significant differences in fasting glycemia (152±32 vs 184±49 mg dl−1, P=0.13; Figure 1c).

Figure 1

Interleukin-18 (IL-18) paradox in diet-induced obesity and cardiac dysfunction. Interleukin-18 (IL-18) knockout (KO) mice had a higher food intake (a) and body weight (b), and similar glucose (c) compared with wild type. IL-18 KO mice presented partially preserved systolic (d) and diastolic function (e–g) and less myocardial interstitial fibrosis (h). #P<0.05 vs wild type; *P<0.05 vs Baseline.

Despite higher caloric intake and weight gain, IL-18 KO mice showed a significantly greater preservation of LV ejection fraction (Figure 1d), reflecting better systolic function, and shorter isovolumetric relaxation time (Figure 1e), lower myocardial performance index (Figure 1f) and lower LVEDP (Figure 1g), reflecting better diastolic function compared with WT mice fed with the same WD. Myocardial interstitial fibrosis was also significantly less in KO compared with WT mice (Figure 1h).

Discussion

These results show the complexity of IL-18 signaling in cardiac function and metabolism. WD impairs cardiac function and promotes obesity through distinct signaling pathways. IL-18 mediates cardiac systolic and diastolic dysfunction induced by WD, providing the possible missing link between the two. IL-18, however, does not mediate the impairment in metabolism nor promotes weight gain seen with WD, while it actually appears to limit these changes.[13] The disconnect between body weight and cardiac function in IL-18 KO mice fed with WD suggests the existence of an 'IL-18-paradox' possibly due to the presence of two different signaling pathways: one leading to cardiac dysfunction and dependent upon IL-18 and one leading to weight gain which is independent of, and actually improved by, IL-18.[13] Mice with genetic deletion of Nod-like receptor pyrin domain-containing protein 3 (NLRP3), the sensor in the NLRP3 inflammasome responsible for the processing of IL-18 and of IL-1β, and mice with genetic deletion of IL-1 have preserved cardiac function and reduced weight gain compared with wild-type mice fed WD,[15, 16, 17, 18] thus suggesting a hierarchy in the response to systemic inflammation by which IL-1β mediates the cardiac effects through activation of IL-18 in the heart[5] and a systemic response that is, at least in part, independent of IL-18 in this model.

This may occur through two different signaling pathways, one in the brain regulating food intake[13] and one in the heart regulating cardiac function[4] (Figure 2). Systemically administered IL-18, indeed, impairs cardiac function,[5] but does not affect food intake,[13] and IL-18 limits food intake only if administered directly in the brain.[13]

Figure 2

Disconnect between the effects of IL-18 deletion on the heart and on metabolism. The disconnect between the effects of IL-18 deletion on the heart and on metabolism suggests the presence of two possible independent pathways: (1) a metabolic pathway, mediated by the central nervous system (CNS), with negative effects of IL-18 deletion on metabolism by increasing food intake, body weight and glucose and (2) a cardiac pathway, with direct protective effect of IL-18 deletion on the heart function by improvement of systolic and diastolic function, and reducing interstitial fibrosis.

The association of obesity and metabolic abnormalities with HF is object of intense investigation, particularly suggesting that obesity causes HF ('obesity cardiomyopathy') and that weight loss would cure HF.[19] However, obesity may also be considered a co-morbid condition that further limits exercise capacity in HF without directly affecting cardiac function.[20]

IL-18 KO mice had better cardiac function despite greater weight gain, showing that in response to WD, obesity and cardiac dysfunction occur simultaneously, yet the former is not the cause for the latter.

The observation that IL-18 KO mice are obese yet have better cardiac function than the leaner WT mice is vaguely reminiscent of the 'obesity paradox' in patients with HF, by which patients with HF and are obese tend to have a more favorable prognosis.[21, 22]

From a translational standpoint, IL-18-targeted strategies may be valuable in preventing or treating heart failure.[4, 23] An IL-18-blocking antibody and recombinant IL-18 binding protein, which binds circulating IL-18 preventing it from binding to the membrane receptor, are being developed as clinical therapeutics. Of note, in preclinical studies[5, 22] and in phase I and II clinical trials,[24, 25] these inhibitors did not impair metabolism nor induce weight gain. This is in contrast with the data from the IL-18 KO mouse model.[13] This substantial difference likely lies in the different IL-18 signaling in the brain, with the IL-18 KO mouse lacking IL-18 throughout the body, including the brain, whereas the antibody and the binding protein fail to cross the blood brain barrier and penetrate the brain and hence have no effect on food intake and weight gain. Similar findings would be expected to be seen in obese subjects, in which we believe that treatment with IL-18-binding protein or IL-18 antibody would still exert beneficial effects on the heart, without inducing an increase in food intake, body weight and impairment in glucose metabolism. A recent pilot study in obese subjects with type 2 diabetes treated with IL-18 antibody for 12 weeks has shown a safe profile of the drug, tested at different doses, without impairing glucose metabolism.[24]

In our study, mice were fed WD for 8 weeks based on our prior study where 4 and 8 weeks of WD induced a significant cardiac dysfunction.[1] We cannot exclude that the cardiac dysfunction induced by WD and the protective effects of IL-18 deletion would differ if mice were fed high-saturated fat and high-sugar diet for a longer period, in which metabolic abnormalities will likely become more prominent. Moreover, we have not measured the levels of other cytokines that may also be involved in the cardiac dysfunction induced by WD and potentially be affected by genetic deletion of IL-18. However, in a prior study the preservation of cardiac function seen in IL-18 KO mouse or after IL-18 blockade therapy did not affect IL-6 plasma levels, suggesting that the protective effects on the heart were independent of IL-6.[5]

Finally, we did not measure the level of oxidative stress induced by high-sugar and high-saturated fat diet, which has also been reported to affect the heart by directly impairing cardiac contractile function,[26] and how the genetic deletion of IL-18 affected such parameters.

In conclusion, IL-18 mediates the cardiac dysfunction induced by a high-saturated fat and high-sugar diet, independent of food intake, obesity and hyperglycemia, showing a disconnect between diet-induced obesity, altered metabolism and cardiac dysfunction.