Amylin Analogues in the Treatment of Diabetes Mellitus: Medicinal Chemistry and Structural Basis of its Function

INTRODUCTION

Diabetes mellitus continues to pose a significant burden on healthcare services worldwide because of its high prevalence. Different management protocols, including diet modification, lifestyle changes, therapeutic regimens have been developed to reduce the signs and symptoms, and hence the severity of diabetes mellitus. Attention has been focused on several bioactive agents that are capable of increasing insulin release especially in type 1 diabetes. One of such agents is amylin. Amylin, also called IAPP (islet amyloid polypeptide) or diabetes-associated peptide, is produced by pancreatic beta cell and co-secreted with insulin. It occurs in the islet of Langerhans of diabetic patients in approximately 1:100 amylin- insulin ratio. It has long been reported that amylin, like amylin beta, known to be associated with Alzheimer’s disease, can induce apoptosis in pancreatic beta cell [1,2]. Amylin was discovered in human in 1987 by Cooper et al [3] and in cats by Westermark et al. [4]

STRUCTURE OF AMYLIN

Amylin is an insoluble protein with a relatively low tissue concentration. Amylin forms long stable fibres which are arranged in regular pattern [5]. It is a small peptide with a molecular weight of only 3.9 kDa [1, 2]. Its amino acid sequence is 46% identical to that of human beta-CGRP (calcitonin-gene related peptide). The ability of amylin to destroy pancreatic beta cell appears to be species specific. For example rat and mice amylin have 3 proline substitutions at amino acid positions 25, 28 and 29. These substitutions have been reported to prevent the development of the fibrillary form of amyloid. The inability of this type of amylin to destroy pancreatic beta cells have been used to development a human amylin analogue capable of stimulating insulin release.

MEDICINAL CHEMISTRY OF AMYLIN

Human amylin has a disulfide bond between cysteine residues 2 and 7. The amidated C-terminal and the disulfide bond must be intact in order for amylin or its analogues to be biologically active [6]. The amino acid sequences of amylin and its analogue (pramlintide) are shown in (Figs. 1, 2).

Since amylin is highly insoluble, and even toxic to pancreatic beta cells because of deposition of fibrillary proteins, an aqueous, non-aggregating form of amylin was established by replacing three amino acid residues. This form of amylin was found to be effective in reducing blood glucose level when given subcutaneously [7].

Pramlintide acetate, a soluble amylin analogue, marketed as Symlin^®, is used as a supplement to insulin in the treatment of type 1 diabetes. For example, co-administration of amylin analogue with insulin to a small cohort of adolescent with type 1 diabetes induced a larger reduction in proprandial hyperglycemia, with a concomitant reduction in the level of glucagon when compared to insulin monotherapy [8, 9]. The actions of amylin and its analogues appear to be synergistic to insulin, with which it is co-released from insulin-producing beta cells after a meal. The positive effect of pramlintide in the treatment of diabetes was acknowledged by an FDA (Food and Drug Administration) approval in March 2005.

Pramlintide, given subcutaneously at a dose of 30 µg per meal, significantly reduced body weight, HbA1c values and even the dosage of insulin [10].

A moderate body weight loss can also be achieved in obese patients with or without diabetes [11]. A major side effect of pramlintide is nausea [12] and vomiting due to a possible excitation of the area postrema [13] in the medulla oblongata

BIOLOGICAL ACTIONS OF NATIVE AMYLIN AND AMYLIN ANALOGUES

RECEPTORS OF AMYLIN

More than six types of amylin receptors AMY1(a), AMY2(a), AMY3(a), AMY1(b) AMY2(b) and AMY3(b) have been identified. These receptors have two units, a calcitonin core surrounded by a receptor activity modifying protein [22]. The receptor activity modifying proteins are divided into 3 classes of proteins that traverse the plasma membrane [23].

AMY1 receptor displays a high affinity for salmon calcitonin, amylin and calcitonin-gene-related peptide but a lower affinity for mammalian calcitonin [24]. The affinity of amylin2 and amylin3 receptors for calcitonin and amylin is similar but lower for calcitonin-gene-related peptide.

Amylin binding sites have been localized to several circumventricular organs, such as the subfornical organ, organum vasculosum lateralis terminalis and the area postrema in the medulla oblongata. These areas are outside of the blood brain barrier, indicating that they will respond to the level of pancreatic beta cell derived amylin [25]

METABOLISM OF AMYLIN

The amylin produced in pancreatic beta cell alongside insulin is eventually excreted by the kidney. Amylin is degraded by insulin-degrading enzyme, a Zn²⁺-rich metalloprotease, which also takes part in the elimination of insulin [26, 27]. Absence of insulin-degrading enzyme in rodents induces glucose intolerance and cerebral accumulation of amyloid beta, whereas effective insulin-degrading enzyme activity reduces accumulation of amyloid.

CONCLUSION

Amylin or diabetes-associated peptide, is co-secreted with insulin in the islet of Langerhans of diabetic patients in approximately 1:100 amylin: insulin ratio. The soluble form of amylin (e.g. pramlintide) is used as a supplement to insulin in the treatment of type 1 diabetes. The actions of amylin analogues appear to be synergistic to that of insulin and can significantly reduce body weight, HbA1c values and even the dosage of insulin.

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