Evidence for beneficial effects of compromised gastric inhibitory polypeptide action in obesity-related diabetes and possible therapeutic implications
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Gastric inhibitory polypeptide (GIP) is a physiological gut peptide secreted from the intestinal K-cells with well documented insulin-releasing actions. However, the GIP receptor is widely distributed in peripheral organs, including the pancreas, gut, adipose tissue, heart, adrenal cortex and brain, suggesting that it may have other functions. The presence of functional GIP receptors on adipocytes and the key role played by GIP in lipid metabolism and fat deposition suggest a possible beneficial effect of compromised GIP action in obesity and insulin resistance. Several key observations in animal models of obesity-related diabetes with chemically or genetically mediated biological GIP deficiency support this concept. Thus, obese diabetic animals with compromised GIP action due to peptide-based GIP receptor antagonists, small molecular weight GIP receptor antagonists, vaccination against GIP, genetic knockout of GIP receptor or targeted K-cell destruction are protected against obesity and associated metabolic disturbances. In addition, by causing preferential oxidation of fat, blockade of GIP signalling clears triacylglycerol deposits from liver and muscle, thereby restoring mechanisms for suppression of hepatic glucose output and improving insulin sensitivity. Emerging evidence also suggests that rapid cure of diabetes in grossly obese patients undergoing bypass surgery is mediated, in part, by surgical removal of GIP-secreting K-cells in the upper small intestine.
KeywordsBypass surgery Gastric inhibitory polypeptide (GIP) GIP receptor Insulin resistance K-cell Obesity Review
Gastric inhibitory polypeptide
G-protein coupled receptor
GIP receptor antagonism with (Proline3)GIP
(Proline3 [Pro3])GIP is a stable and specific antagonist of the GIP receptor and has been shown to effectively antagonise the acute insulinotropic effect of GIP in vitro and in vivo, resulting in acute impairment of glucose tolerance [7, 8]. In normal mice, sustained chemical knockout of GIP receptor signalling results in mild impairment of insulin secretion and glucose homeostasis . However, the metabolic and hormonal disarray of obesity-related diabetes generates an entirely different scenario following long-term disruption of GIP signalling. Thus, as opposed to marginal impairment of glucose homeostasis, the effects of GIP receptor blockade on lipid metabolism and fat deposition significantly improve metabolic status in obesity-related insulin-resistant states. For example, daily administration of (Pro3)GIP for just 11 days to ob/ob mice resulted in significant reduction of hyperglycaemia plus HbA1c and marked improvement of insulin resistance, glucose tolerance and both beta cell morphology and insulin secretion . Furthermore, once-daily administration of the antagonist to young ob/ob mice indicated that compromised GIP action could prevent the onset of hyperglycaemia and associated metabolic abnormalities prior to any effect on body weight .
Studies in wild-type mice with diet-induced obesity-related diabetes illustrate strikingly similar consequences of biological GIP deficiency induced by (Pro3)GIP [12, 13]. Thus, antagonism of GIP receptor by daily injection of (Pro3)GIP was able to essentially reverse or prevent obesity, together with many of the metabolic abnormalities associated with high-fat feeding, e.g. hyperglycaemia, impaired glucose tolerance and dyslipidaemia [6, 12, 13]. A key aspect of these observations was the rapid and significant restoration of insulin sensitivity and depletion of triacylglycerol deposits in liver and muscle. The latter represents a key pathogenic factor, given the well established link between development of insulin resistance and spill over of lipid accumulation at these sites . Lowered glucagon levels could account for part of these observations, but no changes in serum glucagon levels were observed in high-fat fed mice or mice chronically treated with (Pro3)GIP [11, 12, 13].
Further refinement of peptide chemistry may make it possible to increase the potency and duration of action of (Pro3)GIP as a potential biological molecule to induce compromised GIP action. However, there is already little doubt that specific biological GIP receptor antagonists, based on N-terminal modifications of GIP, potentially represent an exciting new class of drugs to combat the obesity-related diabetes epidemic. Studies in human patients will be required to delineate the promise of GIP receptor antagonists. However, the value of therapeutic peptides is well illustrated by the use of insulin for the treatment of type 1 diabetes and their advantage of acting at specific receptors on defined target cells. The main disadvantage is the need for administration by injection.
GIP receptor antagonism using low molecular weight molecules
The potential of low molecular weight receptor ligands for oral administration has often been examined with a view to improving the therapeutic benefit of peptide-based pharmaceuticals and avoiding parenteral administration . Although only reported in preliminary form to date, one study has assessed the metabolic effects of sustained downregulation of GIP signalling using a small molecule GIP receptor antagonist, SKL-14959. Administration of SKL-14959 to high-fat fed mice for 14 weeks significantly reduced body weight gain without affecting food intake . Importantly, and in harmony with studies using (Pro3)GIP, SKL-14959 administration was associated with depressed triacylglycerol accumulation in liver and muscle tissue in high-fat fed mice . In a parallel study using diabetic KKA y mice, 4 weeks oral administration of SLK-14959 significantly decreased plasma glucose and HbA1c levels and ameliorated insulin resistance. These observations were also accompanied by depressed triacylglycerol accumulation in liver . Thus, it appears that chemical GIP receptor blockade using (Pro3)GIP or SLK-14959 is able to clear triacylglycerol deposits from liver of mice that lack GIP effect, thereby restoring mechanisms for suppression of hepatic glucose output. Comparatively very high doses of the small molecule antagonist are needed to induce these effects. Accordingly, further details of specificity, toxicity and chemical identity of SLK-14959 are needed to evaluate the potential therapeutic applicability of this approach, but these early results are encouraging.
Another approach to inhibition of GIP signalling by chemical means is the induction or administration of GIP-specific neutralising antibodies. Two independent ‘proof of concept’ studies have confirmed the therapeutic attractiveness of such approaches for obesity-related diabetes [17, 18]. In a study by Fulurija and colleagues, high titres of specific GIP antibodies were generated by covalent attachment of GIP peptides to virus-like particles followed by subcutaneous vaccination in high-fat fed mice. This resulted in production of GIP antibodies and protection against diet-induced obesity with significantly reduced body fat stores . These observations are similar to those produced by specific chemical GIP receptor blockade in mice with diet-induced obesity [12, 13]. Surprisingly, no benefit on glycaemic control was noted by Fulurija and colleagues, but active GIP immunisation was shown to produce a significant improvement of glucose tolerance and circulating glucose in a separate study in genetically obese ob/ob mice . Thus, vaccination against GIP resulting in antibody production appears to be a practical means of countering the metabolic abnormalities associated with diet- or genetically induced obesity-related diabetes. However further preclinical safety and toxicology studies will be required before the therapeutic concept can be considered in humans.
Inhibition or targeted destruction of GIP-secreting K-cells
An alternative way to downregulate GIP receptor signalling is to inhibit hormone release from intestinal K cells. A potential advantage of this approach is that drugs may be able to target K-cells directly from the intestinal lumen, rather than using systemic delivery of GIP-based peptides or immunogens with the possibility of unwanted side effects at various sites. However, relatively little is known about K-cell signal transduction mechanisms; moreover, given the many similarities with glucagon-like peptide-1 (GLP-1) secretion from L-cells and insulin secretion from beta cells, this approach is unlikely to prove sufficiently specific. For example, although inhibition may be possible by antagonism of G-protein-coupled lipid receptors (GPCR) (i.e. GPCR119, GPCR120 or GPCR40) , the promiscuity of GIP receptors , plus stimulatory effects by other classes of nutrients on GIP secretion represent major obstacles. In addition, the K-cell has also been reported to produce xenin, a hormone that may be involved in glucose regulation and has recently been shown to possess potent inhibitory effects on feeding behaviour in rodents . It is therefore questionable whether such theoretical approaches for GIP blockade are applicable. Notwithstanding this, specific K-cell destruction in transgenic mice with regulatory elements of the GIP promoter/gene expressing an attenuated diphtheria toxin A was shown to protect against diet-induced obesity and ameliorate insulin resistance . Thus, the basic observations with chemical or genetic GIP receptor blockade (see next section) are essentially replicated by targeted knockout of GIP-secreting K-cells in mice fed high-fat diet . Although valuable to reinforce the concept of beneficial effects of compromised GIP action, it seems unlikely that the development of specific K-cell cytotoxic drugs will prove exploitable for therapeutic purposes.
GIP receptor knockout mice
Transgenic mice with knockout of the GIP receptor have been particularly useful in elucidating mechanisms that underlie beneficial effects of compromised GIP action on diet-induced obesity [23, 24]. GIP receptor knockout in mice fed normal diet had little effect, other than small impairment of glucose tolerance and insulin secretion . However, genetic knockout of the GIP receptor in normal or ob/ob mice fed a high-fat diet was shown to decrease respiratory quotient and increase oxygen consumption [23, 24]. This indicates that increased energy expenditure and preferential oxidation of fat as an energy source is key in the beneficial anti-obesity action seen in these animals [23, 24, 26]. This is generally in keeping with the well-known anabolic effects of GIP on lipid metabolism and fat deposition. Thus, inhibition of GIP receptor function in GIP receptor knockout mice fed a high-fat diet resulted in suppression of body weight gain, reduced adiposity, decreased tissue triacylglycerol stores, reduced insulin resistance and marked improvement of glucose tolerance [23, 24]. These observations are very similar to those encountered with chemical GIP receptor blockade. Other indications of altered energy metabolism in GIP receptor knockout mice include increased uncoupling protein-1 and decreased beta-3 adrenergic receptor levels in brown and white adipose tissue, respectively . These data suggest that GIP antagonism enhances energy expenditure in situations of excessive dietary fat intake.
In agreement with these initial observations, a recent study has shown that genetic GIP receptor knockout prevented ovariectomy-induced obesity in mice, extending the same basic observations to distinctly different metabolic settings . It is clear from studies to date using chemical blockade or genetic knockout of GIP signalling that amelioration of insulin resistance is the key element underlying the improvement of metabolic status [10, 13, 16, 23, 24]. Indeed, genetic compromise of GIP signalling has been shown to prevent the development of ageing-associated insulin resistance in mice through changes in body composition and energy expenditure . This is further reinforced by observations that genetic disruption of GIP signalling increased adiponectin levels under conditions of high-fat feeding . Thus, high-fat fed mice exhibited increased fat oxidation in peripheral tissues and decreased triacylglycerol deposition in liver and muscle, together with improved insulin sensitivity [26, 29].
Lessons from animal models
As indicated above, there is now a substantial body of evidence directly linking GIP to the efficient storage of ingested fat, thus conferring a pivotal role for GIP in the development of obesity due to chronic overnutrition with high-fat diets. This contrasts strongly with GLP-1, which does not interact with specific receptors on adipocytes, but exerts glucose-lowering effects through stimulation of insulin secretion and suppression of glucagon, gastric emptying and feeding . Accordingly, inhibition of GIP receptor signalling appears to represent a novel therapeutic strategy for obesity-related diabetes, acting at various sites to improve insulin resistance and pancreatic beta cell function, and to promote depletion of adipose tissue mass (Fig. 1). Importantly, in concurrence with this concept, the complete absence of GIP signalling does not appear to result in any serious adverse effects. Despite the obvious negative effect on the insulinotropic GIP-mediated incretin effect, the beneficial effects of sustained GIP receptor blockade on lipid metabolism and fat deposition considerably offset any such impediments . Moreover, clinical studies have shown that the insulinotropic effect of GIP is already compromised in obesity-related diabetes  and the possibility of upregulation of GLP-1 or neural arms of the enteroinsular axis in GIP receptor knockout mice has been indicated . Improvement of insulin resistance is also linked to lower circulating insulin levels and beta cell rest [10, 11], thereby rendering the loss of any stimulatory effects of GIP on insulin synthesis and beta cell mass, as observed in cellular models [4, 33], less important.
Clearly, further studies are warranted to evaluate the clinical potential of GIP receptor antagonism for human obesity-related diabetes. To date there are no reports of the metabolic consequence of longer-term specific GIP receptor blockade in the clinical setting, although various pharmaceutical companies are involved with the above-mentioned preclinical studies. However, lessons may come from patients undergoing bypass surgery with surgical diversion of nutrient passage away from GIP-secreting K-cells in the upper small intestine [6, 34].
Evidence from human bypass surgery
It has been hypothesised that exclusion of nutrient transit from the upper small intestine results in inhibited secretion of a hormone promoting insulin resistance and deposition of fat stores . Clearly, given the aforementioned array of beneficial effects following GIP receptor blockade in obesity-related diabetes, a reduction in circulating GIP levels by surgical exclusion of the K-cell abundant proximal small intestine could be a key factor in the success of these surgeries . Consistent with this view, several recent studies have shown that GIP is decreased rapidly, in the fasting and most notably postprandial states, following Roux-en-Y and biliopancreatic diversion bypass surgery in humans [34, 35, 36, 37, 43]. Interestingly, in some studies GIP levels were lowered significantly in diabetic, rather than non-diabetic obese patients [35, 36], highlighting the significant role of GIP-mediated actions in this metabolic scenario. In consequence, this kind of surgery can be viewed to reproduce many of the beneficial effects noted in animal models of compromised GIP action, including rapid improvement of insulin resistance and beta cell function (Fig. 2). Nonetheless, it is possible that other important effects are mediated through mechanisms other than GIP, including the surgical ‘knockout’ of an as yet undiscovered hormone from the upper gastrointestinal tract . Interestingly, there appears to be no reduction of GIP levels in other studies, possibly reflecting subtle variations in technique, timing of sample collection, nutritional status and degree of surgical bypass [44, 45].
It is noteworthy that the rapid depletion of hepatic and myocytic triacylglycerol stores for improved metabolic control in bypass surgery patients has been highlighted elsewhere, but attributed to dietary restriction alone . Although severe energy restriction is clearly an important contributor following these surgical procedures , this variable seems unlikely to account for the superior metabolic results of bypass as opposed to restrictive surgery. Nevertheless, it should be remembered that in many cases the gastric band is not adjusted until after several weeks, meaning that energy restriction may be less immediate after this procedure than after bypass surgery. Accordingly, the underlying principles outlined in the current review give credence to the idea that blockade of GIP receptor action offers promise as a new and potentially important approach to obesity-related diabetes. This could be particularly so in obese patients in whom surgery is contraindicated. Indeed given the expense, potential hazards and need for long-term patient management, alternatives to surgery are essential in the management of the obesity-related diabetes epidemic.
Growing evidence supports the view that compromise of GIP action serves to protect against development of obesity and associated metabolic disturbances in times of excessive caloric intake . Thus, GIP appears to directly link overnutrition to obesity and is a potential novel target for anti-obesity-related diabetes drugs. The strikingly similar beneficial effect induced by a wide range of genetic and chemical approaches to impairment of GIP receptor signalling strengthens this belief. Interesting parallels also exist in clinically obese patients undergoing bypass surgery, with diversion of nutrient passage away from the gut section containing GIP-secreting cells. These patients display an unprecedented correction of hyperglycaemia and insulin sensitivity on a par with and possibly even greater than that observed in animal models with disruption of GIP receptor signalling. Further studies are needed to dissect the underlying mechanisms in these patients and to fully delineate the clinical potential of methods of GIP receptor blockade used to date and their possible application in man.
The authors’ work referred to in this review has been generously supported by Diabetes UK, University of Ulster strategic funding, and the SAAD Trading and Contracting Company (Al Khobar, Saudi Arabia).
Duality of interest
The authors hold stock in Diabetica Ltd, which has patents for exploitation of GIP receptor antagonists and other peptide therapeutics. P. R. Flatt also serves on scientific advisory boards and has received speaker’s honoraria and research support from several companies with interests in glucose-lowering drugs and incretin-based therapies, including Astellas, MSD, Novartis, Novo Nordisk, Organon and Schering Plough.
- 8.Gault VA, O'Harte FP, Harriott P, Mooney MH, Green BD, Flatt PR (2003) Effects of the novel (Pro3) GIP antagonist and exendin(9–39) amide on GIP- and GLP-1-induced cyclic AMP generation, insulin secretion and postprandial insulin release in obese diabetic (ob/ob) mice: evidence that GIP is the major physiological incretin. Diabetologia 46:222–230PubMedGoogle Scholar
- 10.Gault VA, Irwin N, Green BD et al (2005) Chemical ablation of gastric inhibitory polypeptide receptor action by daily (Pro3) GIP administration improves glucose tolerance and ameliorates insulin resistance and abnormalities of islet structure in obesity-related diabetes. Diabetes 54:2436–2446PubMedCrossRefGoogle Scholar
- 11.Irwin N, McClean PL, O’Harte FP, Gault VA, Harriott P, Flatt PR (2007) Early administration of the glucose-dependent insulinotropic polypeptide receptor antagonist (Pro3) GIP prevents the development of diabetes and related metabolic abnormalities associated with genetically inherited obesity in ob/ob mice. Diabetologia 50:1532–1540PubMedCrossRefGoogle Scholar
- 12.McClean PL, Irwin N, Cassidy RS, Holst JJ, Gault VA, Flatt PR (2007) GIP receptor antagonism reverses obesity, insulin resistance, and associated metabolic disturbances induced in mice by prolonged consumption of high-fat diet. Am J Physiol Endocrinol Metab 293:E1746–E1755PubMedCrossRefGoogle Scholar
- 13.Gault VA, McClean PL, Cassidy RS, Irwin N, Flatt PR (2007) Chemical gastric inhibitory polypeptide receptor antagonism protects against obesity, insulin resistance, glucose intolerance and associated disturbances in mice fed high-fat and cafeteria diets. Diabetologia 50:1752–1762PubMedCrossRefGoogle Scholar
- 16.Tsubamoto Y, Nakamura T, Kinoshita H, Tanimoto H, Noda H (2008) A novel low-molecular weight antagonist of glucose-dependent insulinotropic polypeptide receptor, SKL14959, prevents obesity and insulin resistance. Diabetologia 51:S373 (Abstract)Google Scholar
- 21.Cooke JH, Patterson M, Patel SR et al (2009) Peripheral and central administration of xenin and neurotensin suppress food intake in rodents. Obesity (Silver Spring). doi: 10.1038/oby2008.652
- 37.Salinari S, Bertuzzi A, Asnaghi S, Guidone C, Manco M, Mingrone G (2009) First-phase insulin secretion restoration and differential response to glucose load depending on the route of administration in type 2 diabetic subjects after bariatric surgery. Diabetes Care 32:375–380PubMedCrossRefGoogle Scholar