Moberg Kerstin Uvnäs
Swedish University of Agriculture, Department of Applied Animal Science and Welfare, Skara, Sweden.
Compr Psychoneuroendocrinol. 2024 Sep 30;20:100268. doi: 10.1016/j.cpnec.2024.100268. eCollection 2024 Nov.
This article summarizes my scientific work and describes some personal experiences during this period. After my basal medical training (MD) (1971), I obtained a PhD in pharmacology (1976) and ended up as a professor of Physiology. My initial studies were within the field of gastroenterology. I showed that the gastrointestinal hormone gastrin, which stimulates HCL secretion in the stomach, was released in response to stimulation of the vagal nerve. Later I showed that the entire endocrine system of the gastrointestinal (GI) tract that promotes digestion and anabolic metabolism and growth was under vagal nerve control. I also showed that activation of the vagal nerve inhibits the function of the inhibitory substance somatostatin. 10 years later, after some big changes in my personal life, my research focus changed. I became interested in female physiology, particularly the role of oxytocin. In addition, I became aware of the situation of female scientists and started to work with questions regarding equality between women and men. I gathered a group of interested female medical students and midwives around me. We demonstrated that breastfeeding and touch (e.g., between mother and baby), via stimulation of sensory nerves in the skin, activated the endocrine system of the GI tract and, thereby, anabolic processes and growth. The effects were exerted via a vagal mechanism and involved activation of parvocellular oxytocinergic neurons from the paraventricular nucleus (PVN). We also showed that the gastrointestinal hormone cholecystokinin stimulated the release of oxytocin in a calorie-dependent way via an afferent vagal mechanism. In summary, there is a bidirectional, vagally mediated connection between the endocrine system of the GI tract and the oxytocin producing neurons in the supraoptic (SON) and paraventricular (PVN) nuclei of the hypothalamus.1. Oxytocinergic neurons from the PVN enhances the activity of the endocrine system of the GI tract and thereby growth and regeneration. The effect is exerted via efferent vagal fibers which inhibit the release of somatostatin. 2. Food in the duodenum triggers a release of cholecystokinin (CCK), which via a vagal afferent mechanism stimulates the release and function of oxytocin. This mechanism is not activated in the absence of food intake. Administration of oxytocin induces a multitude of actions, i.e., anxiolytic and sedative effects, increased pain threshold, lowering of cortisol and blood pressure and an increased activity of the endocrine system of the GI tract. Repeated administration of oxytocin may induce long-term effects and "secondary" mechanisms such as an increased activity of alpha-2- adrenoceptors are involved. Oxytocin released by suckling during breastfeeding or by touch during social interaction will induce a similar effect spectrum. Activation of the parvocellular neurons will stimulate some aspects of social behavior, induce calm and well-being, and decrease levels of fear, stress, and pain. In addition, vagal functions and the activity of the endocrine system of the GI tract will be stimulated. Together, these effects are consistent with the oxytocin-mediated calm and connection response and, in a long-term perspective, with the promotion of well-being and health. A second period of professional difficulties occurred in the late 1990s. I moved to the Swedish University of Agriculture, where I started to investigate the role of oxytocin in interactions between humans and pets, as this type of interaction had been shown to promote health. I continued to study the role of oxytocin in female reproduction, in particular, the role of oxytocin during labor and birth and in the peripartum period. In addition, I started to write books about different aspects of oxytocin. I also wanted to establish a role for oxytocin in the treatment of vaginal atrophy. Several clinical studies show that local intravaginal application of oxytocin in women with vaginal atrophy increases the regeneration of vaginal mucosal cells and function.
本文总结了我的科研工作,并描述了这一时期的一些个人经历。在完成基础医学培训(医学博士,1971年)后,我获得了药理学博士学位(1976年),最终成为一名生理学教授。我最初的研究领域是胃肠病学。我发现,刺激胃中盐酸分泌的胃肠激素胃泌素,会因迷走神经的刺激而释放。后来我发现,促进消化、合成代谢及生长的整个胃肠道内分泌系统都受迷走神经控制。我还发现,迷走神经的激活会抑制抑制性物质生长抑素的功能。10年后,由于我的个人生活发生了一些重大变化,我的研究重点也发生了改变。我开始对女性生理学感兴趣,尤其是催产素的作用。此外,我意识到了女性科学家的处境,并开始研究有关男女平等的问题。我召集了一群感兴趣的女医学生和助产士。我们证明,母乳喂养和触摸(如母婴之间)通过刺激皮肤中的感觉神经,激活了胃肠道内分泌系统,从而促进了合成代谢过程和生长。这些作用是通过迷走神经机制实现的,涉及室旁核(PVN)中促性腺激素释放激素能小细胞神经元的激活。我们还发现,胃肠激素胆囊收缩素通过传入迷走神经机制,以卡路里依赖的方式刺激催产素的释放。总之,胃肠道内分泌系统与下丘脑视上核(SON)和室旁核(PVN)中产生催产素的神经元之间存在双向的、由迷走神经介导的联系。1. 室旁核中的促性腺激素释放激素能神经元增强了胃肠道内分泌系统的活性,从而促进生长和再生。这种作用是通过传出迷走神经纤维实现的,这些纤维会抑制生长抑素的释放。2. 十二指肠中的食物会触发胆囊收缩素(CCK)的释放,CCK通过迷走神经传入机制刺激催产素的释放和功能。在不摄入食物的情况下,这种机制不会被激活。催产素的给药会引发多种作用,即抗焦虑和镇静作用、提高痛阈、降低皮质醇和血压,以及增强胃肠道内分泌系统的活性。重复给予催产素可能会产生长期影响,并涉及“继发性”机制,如α-2肾上腺素能受体活性增加。母乳喂养期间的吮吸或社交互动中的触摸所释放的催产素会引发类似的作用谱。小细胞神经元的激活会刺激社交行为的某些方面,诱导平静和幸福感,并降低恐惧、压力和疼痛水平。此外,还会刺激迷走神经功能和胃肠道内分泌系统的活性。总的来说,这些作用与催产素介导的平静和联系反应一致,从长远来看,与促进幸福感和健康一致。20世纪90年代末,我又遇到了一段职业困境期。我搬到了瑞典农业大学,在那里我开始研究催产素在人与宠物互动中的作用,因为这种互动已被证明能促进健康。我继续研究催产素在女性生殖中的作用,特别是催产素在分娩和围产期的作用。此外,我开始撰写关于催产素不同方面的书籍。我还想确定催产素在治疗阴道萎缩中的作用。几项临床研究表明,对患有阴道萎缩的女性进行阴道局部应用催产素,可以增加阴道黏膜细胞的再生和功能。