Kitazawa Takio, Kaiya Hiroyuki
Comparative Animal Pharmacology, Department of Veterinary Science, Rakuno Gakuen University, Ebetsu, Japan.
Department of Biochemistry, National Cerebral and Cardiovascular Center Research Institute, Suita, Japan.
Front Endocrinol (Lausanne). 2019 May 17;10:278. doi: 10.3389/fendo.2019.00278. eCollection 2019.
The energy balance of vertebrates is regulated by the difference in energy input and energy expenditure. Generally, most vertebrates obtain their energy from nutrients of foods through the gastrointestinal (GI) tract. Therefore, food intake and following food digestion, including motility of the GI tract, secretion and absorption, are crucial physiological events for energy homeostasis. GI motility changes depending on feeding, and GI motility is divided into fasting (interdigestive) and postprandial (digestive) contraction patterns. GI motility is controlled by contractility of smooth muscles of the GI tract, extrinsic and intrinsic neurons (motor and sensory) and some hormones. In mammals, ghrelin (GHRL) and motilin (MLN) stimulate appetite and GI motility and contribute to the regulation of energy homeostasis. GHRL and MLN are produced in the mucosal layer of the stomach and upper small intestine, respectively. GHRL is a multifunctional peptide and is involved in glucose metabolism, endocrine/exocrine functions and cardiovascular and reproductive functions, in addition to feeding and GI motility in mammals. On the other hand, the action of MLN is restricted and species such as rodentia, including mice and rats, lack MLN peptide and its receptor. From a phylogenetic point of view, GHRL and its receptor GHS-R1a have been identified in various vertebrates, and their structural features and various physiological functions have been revealed. On the other hand, MLN or MLN-like peptide (MLN-LP) and its receptors have been found only in some fish, birds and mammals. Here, we review the actions of GHRL and MLN with a focus on contractility of the GI tract of species from fish to mammals.
脊椎动物的能量平衡由能量输入与能量消耗的差异来调节。一般来说,大多数脊椎动物通过胃肠道(GI)从食物营养中获取能量。因此,食物摄入以及随后的食物消化,包括胃肠道的蠕动、分泌和吸收,都是能量稳态的关键生理事件。胃肠道蠕动会根据进食情况而变化,并且胃肠道蠕动可分为空腹(消化间期)和餐后(消化期)收缩模式。胃肠道蠕动受胃肠道平滑肌的收缩性、外在和内在神经元(运动和感觉神经元)以及一些激素的控制。在哺乳动物中,胃饥饿素(GHRL)和胃动素(MLN)刺激食欲和胃肠道蠕动,并有助于能量稳态的调节。GHRL和MLN分别在胃黏膜层和小肠上段产生。GHRL是一种多功能肽,除了在哺乳动物的进食和胃肠道蠕动方面发挥作用外,还参与葡萄糖代谢、内分泌/外分泌功能以及心血管和生殖功能。另一方面,MLN的作用较为局限,像啮齿动物(包括小鼠和大鼠)等物种缺乏MLN肽及其受体。从系统发育的角度来看,已在各种脊椎动物中鉴定出GHRL及其受体GHS - R1a,并揭示了它们的结构特征和各种生理功能。另一方面,仅在一些鱼类、鸟类和哺乳动物中发现了MLN或类胃动素肽(MLN - LP)及其受体。在此,我们重点回顾从鱼类到哺乳动物的物种胃肠道收缩性方面GHRL和MLN的作用。