Lutz T A, Rand J S
Institute of Veterinary Physiology, University of Zůrich, Switzerland.
Vet Clin North Am Small Anim Pract. 1995 May;25(3):527-52. doi: 10.1016/s0195-5616(95)50051-8.
Cats are one of the few species that develop a form of diabetes mellitus that is clinically and histologically analogous to human type 2 diabetes mellitus. Figure 9 summarizes the etiologic factors thought to be involved in the development of feline and human type 2 diabetes. The main metabolic characteristics of type 2 diabetes mellitus are impaired insulin secretion and resistance to the action of insulin in its target tissues. Impaired beta cell function occurs before histologic changes become evident. The characteristic histologic finding in cats with type 2 diabetes is deposition of amyloid in pancreatic islets. Amyloid deposition occurs before the onset of clinical signs, but does not seem to be the primary defect. Pancreatic amyloid is derived form the recently discovered pancreatic hormone amylin. Amylin is synthesized in pancreatic beta cells, and is co-stored and co-secreted with insulin. Amylin has been postulated to be involved in the pathogenesis of feline diabetes mellitus both through its metabolic effects, which include inhibition of insulin secretion and induction of insulin resistance, and via progressive amyloid deposition and beta cell degeneration. Increased amylin concentration has been documented intracellularly in cats with impaired glucose tolerance and in the plasma of diabetic cats, and supports the hypothesis that amylin is involved in the pathogenesis of type 2 diabetes. Obesity is a common finding in diabetic felines and is a contributing factor to the insulin resistance present in type 2 diabetes. Clinical signs of diabetes develop once total insulin secretion decreases to 20% to 25% of normal levels. Many diabetic cats have been treated successfully with oral hypoglycemics, but 50% to 70% of diabetic cats are insulin dependent. Based on histologic evidence, this is the result of extensive amyloid deposition and subsequent beta cell degeneration, rather than autoimmune destruction of pancreatic beta cells associated with type 1 diabetes. Alternative ways of treating type 2 diabetes currently are being investigated. Amylin antagonists recently have been proposed as a novel treatment to reverse the deleterious effects of excessive amylin concentrations. The gastrointestinal hormone glucagon-like peptide-1 may also prove useful in treating diabetic cats, because of its stimulatory effect on insulin secretion and synthesis, and the absence of significant hypoglycemic effect.
猫是少数会患上一种糖尿病的物种之一,这种糖尿病在临床和组织学上与人类2型糖尿病相似。图9总结了被认为与猫和人类2型糖尿病发生有关的病因。2型糖尿病的主要代谢特征是胰岛素分泌受损以及对其靶组织中胰岛素作用的抵抗。在组织学变化明显之前,β细胞功能就已受损。2型糖尿病猫的特征性组织学发现是胰岛中淀粉样蛋白的沉积。淀粉样蛋白沉积在临床症状出现之前就已发生,但似乎不是主要缺陷。胰腺淀粉样蛋白源自最近发现的胰腺激素胰淀素。胰淀素在胰腺β细胞中合成,并与胰岛素共同储存和共同分泌。有人推测,胰淀素通过其代谢作用(包括抑制胰岛素分泌和诱导胰岛素抵抗)以及通过渐进性淀粉样蛋白沉积和β细胞变性,参与了猫糖尿病的发病机制。在糖耐量受损的猫的细胞内以及糖尿病猫的血浆中,已记录到胰淀素浓度升高,这支持了胰淀素参与2型糖尿病发病机制的假说。肥胖在糖尿病猫中很常见,并且是2型糖尿病中存在的胰岛素抵抗的一个促成因素。一旦总胰岛素分泌降至正常水平的20%至25%,糖尿病的临床症状就会出现。许多糖尿病猫已通过口服降糖药成功治疗,但50%至70%的糖尿病猫依赖胰岛素。基于组织学证据,这是广泛淀粉样蛋白沉积和随后β细胞变性的结果,而不是与1型糖尿病相关的胰腺β细胞自身免疫性破坏。目前正在研究治疗2型糖尿病的替代方法。最近有人提出胰淀素拮抗剂作为一种新的治疗方法,以逆转胰淀素浓度过高的有害影响。胃肠激素胰高血糖素样肽-1可能也被证明对治疗糖尿病猫有用,因为它对胰岛素分泌和合成有刺激作用,且没有明显的低血糖作用。