Hypertension represents a major risk factor for several heart diseases and an important contributor to HFpEF [4], showing a prevalence of 55–86 % in HFpEF patients [4]. Thus, not surprisingly, many models of HFpEF have hitherto involved studies of increased afterload and LV concentric hypertrophy (i.e. transverse-aortic constriction or systemic arterial hypertension) [4].

The Dahl salt-sensitive (SS) rat was selectively bred from Sprague-Dawley presenting the highest values of blood pressure. Dahl/SS is characterised by hypersensitivity to sodium intake and represents the most published HFpEF animal model [6]. When fed with a high-salt diet (8 % NaCl) from the age of 7 weeks, Dahl/SS rats develop renal failure, fast-developing hypertension (> 175 mmHg) and LV hypertrophy, falling into HFpEF between 12 and 19 weeks of age [6]. At week 12, Dahl/SS rats develop diastolic dysfunction such as increased chamber stiffness (left and upward shift of end-diastolic pressure-volume relationship (EDPVR) and decrease of end-diastolic volume). Between 16 and 20 weeks, Dahl/SS hearts enlarge so that end-diastolic volumes and EDPVRs become similar to the respective age-matched controls. Concomitantly, overall pump function curves move towards control, and ejection fraction declines, thus, progressing towards HFrEF. Despite normal or enhanced overall pump function at a certain time-point, LV end-diastolic pressure (LVEDP) and wet lung weight increases, indicating the development of heart failure. Caution should be taken as some authors report HFrEF rather than HFpEF in Dahl/SS. It appears that subtle differences in the experimental design, such as the specific genetic background of the animals as well as environmental conditions, including diet, may importantly impact the cardiovascular phenotype of Dahl/SS.

The deoxycorticosterone acetate (DOCA) salt-induced rat model represents a pharmacologically induced model of hypertension. DOCA is administered by intraperitoneal or subcutaneous injection at 7 weeks of age, 1 week after a unilateral nephrectomy. This combination results in hypertension, renal hypertrophy, nephrosclerosis, cardiac hypertrophy and perivascular fibrosis within 4–5 weeks of chronic DOCA treatment [7]. It is used in rats and mice, and isotonic saline is the sole drinking fluid, which accelerates and aggravates hypertension progression [8]. The DOCA-salt hypertensive rat develops myocardial inflammation, oxidative stress, fibrosis and diastolic dysfunction. Diastolic dysfunction was confirmed by impaired relaxation (higher E/E’ and time constant of isovolumetric relaxation - τ) and increased stiffness (elevated EDPVR slope) compared to control subjects [8] and this seems to be related with the impact of oxidative stress on myofilamentary proteins [8]. Subsequently, a related model was developed, consisting of exposure to 2 weeks of transverse-aortic constriction prior to DOCA administration, demonstrating normal LV systolic pressure and fractional shortening but more hypertrophy, fibrosis and diastolic dysfunction (higher LVEDP and EDPVR) with increased lung weight, consistent with HFpEF [9].

Chronic stimulation with pro-hypertrophic agents, such as angiotensin II and isoprenaline, has been used as a model of systolic and diastolic dysfunction as well as LV hypertrophy. Angiotensin II-treated rodents show evidence of hypertension, increased LV hypertrophy, fibrosis and expression of natriuretic peptides, which result in diastolic dysfunction confirmed by increase/worsening in LV isovolumetric relaxation time (IVRT), myocardial performance index, τ, LVEDP, E/E’ along with decreased E/A, without changes in LV dimensions, mass, or ejection fraction [10]. In the same way, the use of isoprenaline displayed cardiac hypertrophy, myocardial fibrosis and decreased ventricular relaxation [11]. Notwithstanding, blockers of the renin-angiotensin-aldosterone system or β-adrenergic receptors have not demonstrated appreciable benefit in patients with HFpEF.

Transverse-aortic constriction is a well-established surgical technique for inducing LV chronic pressure overload and hypertrophy in rodents. Moderate transverse-aortic constriction imposed at an early age triggers concentric LV hypertrophy with compensated chamber performance, markedly with prominent diastolic filling abnormalities. Transmitral flow profile showed a ‘restrictive’ filling pattern with increased early (E-wave) and decreased late (A-wave) diastolic transmitral filling velocities, augmented E/E’ and left atrial diameter, more rapid deceleration of the early filling wave as well as a shortened IVRT. These abnormalities became progressively more exaggerated at 12 and 18 weeks [12], thus representing a good model for studying HFpEF. The transition from compensated hypertrophy to early failure (HFrEF) is heralded by LV dilation, impairment of systolic function and progression of the abnormal filling [12].

A major limitation of using aortic-banded or hypertensive models is that the majority of patients with HFpEF continue to have heart failure symptoms even when the blood pressure is controlled. Conversely, less than 50 % of HFpEF patients have LV hypertrophy and often show no evidence of LV dilatation, thus making the value of the current preclinical model questionable [13].

Approximately one-third of HFpEF patients have type 2 DM and cardiovascular disease is the leading cause of morbidity and mortality in diabetic patients. Interestingly, diastolic dysfunction represents an early cardiac manifestation of the deleterious effects of DM, since young diabetic individuals predominantly display diastolic abnormalities, whereas HFrEF rarely develops before middle age in obese diabetic individuals [14]. Insulin resistance, type 2 DM and hyperinsulinaemia exert a number of pleiotropic effects on the myocardium, including stimulation of hypertrophy, increased oxidative stress and proinflammatory/profibrotic effects, which can induce deleterious changes in cardiomyocyte function as well as in the extracellular matrix [15].

Many models of type 2 DM recapitulate the features of HFpEF patients, including leptin-deficient ob/ob mice and the leptin receptor-deficient db/db mice, whose altered leptin homeostasis leads to obesity due to hyperphagia, hyperglycaemia, hyperinsulinaemia, insulin resistance and diabetic complications at different time points [16].

Db/db mice develop cardiac hypertrophy as evidenced by increased LV mass and wall thickness at 9 weeks of age, which is associated with a smaller LV end-diastolic volume. The progression of diabetic cardiomyopathy is accompanied by increased production of reactive oxygen species and interstitial fibrosis [17]. Five-month-old mice display haemodynamic alterations such as elevated LVEDP and EDPVR, reduced dP/dt_min, and prolonged relaxation. At this age, transthoracic echocardiography confirmed preserved systolic function with elevated IVRT and reduced E/A, clearly indicating diastolic dysfunction [17]. The administration of angiotensin II for 4 weeks in db/db mice induced the expression of markers of hypertrophy and fibrosis but did not impact greatly on cardiac structure or lead to HFpEF [18].

Ob/ob mouse is an obesity and diabetic animal model that shows evidence of diastolic dysfunction possibly due to cardiac lipid accumulation [19]. Ob/ob mice develop myocardial hypertrophy and triglyceride accumulation, which parallels LV diastolic dysfunction as confirmed by decreased E/A [19]. Progressively, this animal model develops diabetic cardiomyopathy with impaired contractility and relaxation [20].

The increase in global incidence of obesity predicts a continuous rise of the burden of cardiovascular diseases. This is particularly true for HFpEF, as obesity has a prevalence of 41–46 %, is associated with an increased risk of hypertension, dyslipidaemia and diabetes and thus represents an independent risk factor for its development [21]. Many available models of obesity are derived from selective crossing between rats comprising one out of the two most significant mutations in leptin receptor (i.e. fa and cp). These models are usually associated with other risk factors, including hypertension and/or diabetes, with some of them developing diastolic dysfunction or HFpEF.

Zucker rats were originally bred to be a genetic model of obesity and hypertension. The obese Zucker rat demonstrates a consistent increase in LV mass and early diastolic dysfunction with prolonged IVRT [22]. In contrast, the obese diabetic Zucker (ZDF) rat does not develop increased LV mass even though mild hypertension is present and diastolic dysfunction is evident [23].

The Otsuka Long-Evans Tokushima Fatty (OLETF) rat was derived by selecting spontaneously diabetic rats displaying polyuria, polydipsia and obesity from an outbred colony of Long-Evans rats [24]. The OLETF rat is used as a model of diabetic cardiomyopathy and displays echocardiographic evidence of diastolic dysfunction from 20 weeks of age as observed by deceleration time of the E-wave and decreased E/A [25].

Dahl/SS/obese rats, derived from Dahl/SS and Zucker crossing, have been recently established as a new model of metabolic syndrome. At 15 weeks of age, female Dahl/SS/obese rats present with LV diastolic dysfunction, marked LV hypertrophy and fibrosis, associated with increased cardiac oxidative stress and inflammation [26].

A recently discovered HFpEF model is the obese ZSF1 rat. The ZSF1 rat was generated by crossing non-hypertensive lean female Zucker diabetic fatty rats (ZDF, +/fa) with lean spontaneously hypertensive heart failure prone male rats (SHHF/Mcc, +/facp), sharing a common genetic background with Wistar Kyoto rats [27]. Both lean and obese ZSF1 animals inherit a hypertensive gene from the spontaneously hypertensive rat strain and show elevated blood pressure [27]. The 20-week-old obese ZSF1 rat represents a robust model of metabolic syndrome since it displays hypertension, obesity, type 2 DM, insulin resistance, hyperinsulinaemia, hypertriglyceridaemia, hypercholesterolaemia and heart failure. Considering such features, this cardiometabolic risk model develops diastolic dysfunction such as prolonged τ, an upwards shift of EDPVR and elevated arterial elastance. Along with higher resting LVEDP, obese ZSF1 rats show reduced effort tolerance and VO₂max, showing, for the first time in an animal model, an important corresponding feature of HFpEF human diagnosis - exercise intolerance. In parallel, there is LV hypertrophy and left atrial dilation (Fig. 2), without signs of renal failure at 20 weeks of age [28]. In male obese ZSF1 rats, the increased myocardial stiffness appears mostly due to myofilament changes, without significant interstitial fibrosis [28]. A subgroup of ZSF1 obese rats subjected to a Western high-fat diet for 10 weeks showed no further aggravation of HFpEF phenotype [28].

The prevalence of HFpEF in the community increases with advancing age and is higher in women. Indeed, the reported age- and sex-specific prevalence for individuals 80 years and older is about 4–6 % in men and 8–10 % in women [21]. Thus, ageing models are important to understand the pathophysiology of age-related diastolic dysfunction.

The spontaneous senescence-prone (SAMP8) mouse offers a good model of cardiac dysfunction associated with ageing. At 6 months of age, this animal model displayed a significant reduction of E/A ratio, E’ and E’/A’ along with increased EDPVR, fibrosis and TGF-β expression when compared to the control group (SAMR1). No differences in systolic function or mean arterial pressure were reported in SAMP8 mice [29].

FVB/N mice represent a robust inbred strain and males display diastolic dysfunction at 12 months, with an E/A < 1 while, in females, this phenotype is not observed [30]. In contrast, Fischer 344 ageing rats showed more prominent LV hypertrophy and diastolic dysfunction in females compared to males, as assessed by increased IVRT and decreased septal E’. Instead, males displayed fibrosis and systolic dysfunction [31]. Other studies aiming to evaluate age-related cardiac changes using male Fischer 344/Brown Norway F1 rats revealed a decline in cardiac function and LV structural changes, compatible with the phenotype of HFpEF [32].

A considerable number of aortic banding studies have been performed and many have yielded significant insights into the pathophysiology of HFpEF, well before the actual term was even established. The most consistent finding from pressure-overload studies is the principally concentric type of LV hypertrophy that is produced and which is often observed in HFpEF. In addition, these studies [33‐35] have revealed the presence of impaired myocardial blood flow reserve, particularly during exercise, impaired endothelial function of large coronary artery, enhanced apoptosis, abnormalities in bioenergetics and metabolism, exhausted myocardial perfusion and exaggerated oxygen consumption during exercise, all of which are likely contributors to diastolic dysfunction in this model [36]. Nonetheless, cardiac dysfunction is often variable, as in patients, and not always even evident as assessed in vivo although abnormalities at the myocyte level are still present [37]. Furthermore, these earlier studies concentrated mostly on functional aspects and, apart from increased fibrosis [38], histological information from these studies remains limited. Increased LV fibrosis was documented by Yarborough et al. who also reported increased LV diastolic stiffness in a model of HFpEF induced by progressive aortic cuff inflation [39]. In their study, increased LV fibrosis was due to enhanced collagen stability but not its expression, and collagen content correlated with myocardial stiffness [39]. Aortic banding-induced HFpEF was recently investigated by Emter and colleagues [33, 38]. In support of earlier findings, these authors documented enhanced fibrosis in the left ventricle of aortic banded swine, but also showed that exercise training is a promising treatment in HFpEF, as it promotes compliant extracellular matrix fibrotic components and preserves extracellular matrix regulatory mechanisms. In addition, exercise training preserved myocardial oxygen balance, and promoted physiological molecular hypertrophic signalling cardiac phenotype [33, 38]. This is important, as no proven pharmacological treatments have yet been reported for HFpEF.

Renal wrapping-induced hypertension has been extensively used in dogs. Hart and colleagues reported that this model increased LV fibrosis and mass, which was accompanied by elevations in LVEDP 12 weeks after renal wrapping [40]. In their study, LV end-diastolic volume, ejection fraction, stroke volume, cardiac output and neurohumoral activity including circulating angiotensin II, endothelin and catecholamine levels as well as plasma renin activity were all comparable with control levels [40]. In contrast, humoral activation (renin activity, aldosterone, brain natriuretic peptide and adrenomedullin) was increased in bilateral renal wrapping performed by Maniu and colleagues [41]. To our knowledge, the first large animal study designed to specifically address HFpEF was performed by Munagala et al. [42], who showed that bilateral renal wrapping-induced hypertension resulted in increased arterial stiffness, associated with an increased LV mass and fibrosis in old dogs, although LV volume and also LV diastolic stiffness were similar to healthy controls [42]. These authors also reported enhanced end-systolic elastance in this model of HFpEF. Renal wrapping in dogs has also been studied by Hayashida and colleagues, for testing of novel pharmacological treatments for HFpEF [43], and this model continues to be used. Renal wrapping was also applied in an early study in nonhuman primates by Abrahams and colleagues, who observed a progressive increase in LV collagen content, with cardiomyocytes ultimately becoming encased by collagen after 80 weeks of follow-up [44].

In comparison with studies in rodent models (Table 1), obesity or metabolic syndrome (such as high fat diet alone or in combination with experimental diabetes) induced HFpEF has been sparsely studied in large animal models. Diastolic dysfunction, albeit in a variable degree, was however documented recently in type 2 DM rhesus monkeys (Table 2), although LV histology was performed in only one diseased animal [45]. Furthermore, several large animal models with features of metabolic syndrome have demonstrated alterations in coronary vascular function and structure. For instance, Trask et al. described in obese Ossabaw swine with metabolic syndrome an hypertrophic inward remodelling of coronary resistance microvessels along with coronary capillary rarefaction, which was associated with a decrease in coronary flow and myocardial ischaemia [46]. In a pre-atherosclerotic diabetes mellitus porcine model with type 2 characteristics small coronary arteries displayed reduced nitric oxide bioavailability and loss of endothelin-1 response [47]. Unfortunately, cardiac function was not investigated, and thus future studies are required to assess the impact of these coronary vascular abnormalities on cardiac function.

With advancing age, the cardiovascular system is known to stiffen, while the prevalence of HFpEF increases. Hence, ageing dogs have been used to investigate the effect of age on features of HFpEF. Ageing alone did not have a major influence on LV structure and function in the study by Munagala et al., but the combination of old age and renal wrapping resulted in impairments in diastolic function although myocardial fibrosis was similar to control levels [42], suggesting that hypertension rather than age was the causal factor [42]. Conversely, a decrease in LV distensibility was observed in aged compared to young dogs, which was accompanied by an increase in LVEDP and a decrease in LV end-diastolic volume [48]. As ejection fraction and LV mass were not affected, this model recapitulates several aspects of HFpEF and may prove useful in future studies.