Evolutionary physiology

IF 5.6 2区 医学 Q1 PHYSIOLOGY Acta Physiologica Pub Date : 2024-08-29 DOI:10.1111/apha.14221
Pontus B. Persson, Anja Bondke Persson
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Some authors attribute the development or emergence of evolutionary physiology as a subspecialty to the late 1980s<span><sup>2</sup></span> as a field which integrates perspectives from genetics, ecology, and evolutionary biology to understand the origins, adaptability and maintenance of physiological diversity. Svante Pääbo, so-called “reader of the Neanderthal genome,”<span><sup>3</sup></span> may be seen as a prime example who opened the door to ancient genomics. However, for a study to touch upon evolutionary physiology, it does not necessarily have to focus primarily on elucidating developments from eons past. In this paper, we take a closer look at recent publications, which aim to investigate the physiological adaptations and trade-offs that have arisen through natural selection, shedding light on evolutionary pathways, outcomes and perspectives.</p><p>Recent developments, including climate change, are increasingly recognized as significant drivers of evolutionary processes in various species. These environmental changes create new selective pressures, leading to adaptations that can alter genetic diversity and influence species' survival and reproduction.<span><sup>4</sup></span> The study by Sokolova et al. sheds light on the impact of environmental temperature changes on energy metabolism and thus on the mitochondrial function.</p><p>Mitochondria, usually introduced in Bio 101 classes as cellular power plants, are in themselves almost bizarre examples of evolutionary development. Other entities within the mammalian organism are also of questionable descent, such as retrovirus-like Gag Protein Arc1, which—and we do not know why—bears a domain which resembles retroviral/retrotransposon -like proteins, which multimerize into a capsid that packages viral RNA.<span><sup>5</sup></span> Most likely, once upon a time, mitochondria started out as α-Proteobacteria. Until recently, the most common theory was an endosymbiont hypothesis, that is, an incorporation of bacterial cell compounds into eukaryotic cells. Recently, however, evidence has emerged which prompts the question of whether the mitochondrion really emerged after the eukaryotic cell, or if this organelle even originated simultaneously with the cell that contains it.<span><sup>6</sup></span> Nevertheless, mitochondrial bacterial characteristics, such as cytosine-phosphate-guanosine, the membrane lipid cardiolipin, N-formylated peptides and circular double-stranded DNA may be responsible for inducing or perpetuating inflammatory processes following mitochondrial damage.<span><sup>7</sup></span></p><p>Human energy metabolism is in itself a focus topic touching heavily on evolutionary physiology: Brown adipose tissue (BAT) expresses thermogenic uncoupling protein 1 (UCP1), enabling humans to maintain their body temperatures during cold stress.</p><p>As it has recently emerged how adults retain BAT, which may play a role in non-shivering thermogenesis, it has been hypothesized that BAT plasticity was a main factor in allowing human populations expansion into circumpolar regions.<span><sup>8</sup></span> Recently developed UCP-1 deficient animal models allow a closer look at non-shivering thermogenesis<span><sup>9</sup></span> and thermogenic adaptation to cold challenges,<span><sup>10</sup></span> and further insights into the evolution of mammalian brown fat (non-shivering) thermogenesis,<span><sup>11</sup></span> 50 years after the identification and description of UCP-1.<span><sup>12</sup></span></p><p>Also, mitochondria seem to be critically involved in the evolutionary adaptation of vertebrates to hypoxic or even anoxic environments,<span><sup>13</sup></span> comprising mainly cardiorespiratory<span><sup>14, 15</sup></span> as well as neuromuscular<span><sup>16</sup></span> adaptations.</p><p>During mammalian evolution, the utilization of oxygen and nutrients, as exemplified above, was adapted, as was the excretion of metabolic waste. In Book XXXI of his Natural History, Pliny the Elder mentioned a salt he named “<i>hammoniacum</i>,” which is thought to have derived its name from its proximity to the Temple of Jupiter Amun (Ἄμμων Ammon in Greek), which was located in the Roman province of Cyrenaica.<span><sup>17</sup></span> The precise nature of this salt remains uncertain; however, it is the etymological origin of the names for ammonia and ammonium compounds. Ammonia is one of the so-called “nitrogen wastes,” which, together with urea, uric acid, and creatinine result from mammalian protein metabolism and must be excreted to avoid toxicity, processes whose evolutionary origins and development have recently been elucidated in intriguing detail.<span><sup>18-20</sup></span></p><p>The evolution of another characterizing function of most higher organisms, circadian rhythm, is thought to have provided organisms with a survival advantage by synchronizing physiological processes and behavior with the predictable cycles of the environment, such as day and night. Circadian clocks are present in most light-sensitive organisms, from simple unicellular entities to humans, and probably provide an evolutionary advantage by enabling organisms to anticipate and proactively respond to challenges arising from their cyclic environment.<span><sup>21</sup></span> Modern environments, mostly indirect results of human evolution, with artificial lighting and irregular schedules, can disrupt natural circadian rhythms, leading to potential behavioral and health-related consequences.<span><sup>22</sup></span></p><p>In summary, these studies highlight the intricate relationship between physiology and evolution, demonstrating how organisms adapt to their environments through physiological modifications. By examining the evolutionary pathways and trade-offs that shape physiological traits, we gain a deeper understanding of the mechanisms underlying physiological diversity. 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引用次数: 0

Abstract

Evolution, a “process of heritable change in populations of organisms over multiple generations […] through mechanisms including natural selection, sexual selection and genetic drift,”1 is the unifying framework that explains the diversity of life, guiding our understanding of biological processes, species interactions, and the development of new medical and biotechnological innovations. Evolutionary physiology is a multidisciplinary field that explores how organisms adapt their physiological functions to changing environmental conditions. Some authors attribute the development or emergence of evolutionary physiology as a subspecialty to the late 1980s2 as a field which integrates perspectives from genetics, ecology, and evolutionary biology to understand the origins, adaptability and maintenance of physiological diversity. Svante Pääbo, so-called “reader of the Neanderthal genome,”3 may be seen as a prime example who opened the door to ancient genomics. However, for a study to touch upon evolutionary physiology, it does not necessarily have to focus primarily on elucidating developments from eons past. In this paper, we take a closer look at recent publications, which aim to investigate the physiological adaptations and trade-offs that have arisen through natural selection, shedding light on evolutionary pathways, outcomes and perspectives.

Recent developments, including climate change, are increasingly recognized as significant drivers of evolutionary processes in various species. These environmental changes create new selective pressures, leading to adaptations that can alter genetic diversity and influence species' survival and reproduction.4 The study by Sokolova et al. sheds light on the impact of environmental temperature changes on energy metabolism and thus on the mitochondrial function.

Mitochondria, usually introduced in Bio 101 classes as cellular power plants, are in themselves almost bizarre examples of evolutionary development. Other entities within the mammalian organism are also of questionable descent, such as retrovirus-like Gag Protein Arc1, which—and we do not know why—bears a domain which resembles retroviral/retrotransposon -like proteins, which multimerize into a capsid that packages viral RNA.5 Most likely, once upon a time, mitochondria started out as α-Proteobacteria. Until recently, the most common theory was an endosymbiont hypothesis, that is, an incorporation of bacterial cell compounds into eukaryotic cells. Recently, however, evidence has emerged which prompts the question of whether the mitochondrion really emerged after the eukaryotic cell, or if this organelle even originated simultaneously with the cell that contains it.6 Nevertheless, mitochondrial bacterial characteristics, such as cytosine-phosphate-guanosine, the membrane lipid cardiolipin, N-formylated peptides and circular double-stranded DNA may be responsible for inducing or perpetuating inflammatory processes following mitochondrial damage.7

Human energy metabolism is in itself a focus topic touching heavily on evolutionary physiology: Brown adipose tissue (BAT) expresses thermogenic uncoupling protein 1 (UCP1), enabling humans to maintain their body temperatures during cold stress.

As it has recently emerged how adults retain BAT, which may play a role in non-shivering thermogenesis, it has been hypothesized that BAT plasticity was a main factor in allowing human populations expansion into circumpolar regions.8 Recently developed UCP-1 deficient animal models allow a closer look at non-shivering thermogenesis9 and thermogenic adaptation to cold challenges,10 and further insights into the evolution of mammalian brown fat (non-shivering) thermogenesis,11 50 years after the identification and description of UCP-1.12

Also, mitochondria seem to be critically involved in the evolutionary adaptation of vertebrates to hypoxic or even anoxic environments,13 comprising mainly cardiorespiratory14, 15 as well as neuromuscular16 adaptations.

During mammalian evolution, the utilization of oxygen and nutrients, as exemplified above, was adapted, as was the excretion of metabolic waste. In Book XXXI of his Natural History, Pliny the Elder mentioned a salt he named “hammoniacum,” which is thought to have derived its name from its proximity to the Temple of Jupiter Amun (Ἄμμων Ammon in Greek), which was located in the Roman province of Cyrenaica.17 The precise nature of this salt remains uncertain; however, it is the etymological origin of the names for ammonia and ammonium compounds. Ammonia is one of the so-called “nitrogen wastes,” which, together with urea, uric acid, and creatinine result from mammalian protein metabolism and must be excreted to avoid toxicity, processes whose evolutionary origins and development have recently been elucidated in intriguing detail.18-20

The evolution of another characterizing function of most higher organisms, circadian rhythm, is thought to have provided organisms with a survival advantage by synchronizing physiological processes and behavior with the predictable cycles of the environment, such as day and night. Circadian clocks are present in most light-sensitive organisms, from simple unicellular entities to humans, and probably provide an evolutionary advantage by enabling organisms to anticipate and proactively respond to challenges arising from their cyclic environment.21 Modern environments, mostly indirect results of human evolution, with artificial lighting and irregular schedules, can disrupt natural circadian rhythms, leading to potential behavioral and health-related consequences.22

In summary, these studies highlight the intricate relationship between physiology and evolution, demonstrating how organisms adapt to their environments through physiological modifications. By examining the evolutionary pathways and trade-offs that shape physiological traits, we gain a deeper understanding of the mechanisms underlying physiological diversity. These findings underscore the importance of considering evolutionary history in physiological studies and provide a foundation for future research in this dynamic and integrative field. As we continue to explore the complexities of evolutionary physiology, we can better appreciate the adaptive strategies that enable species to thrive in a constantly changing world.

None.

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进化生理学
进化是 "通过自然选择、性选择和遗传漂变等机制,在生物种群中经过多代[......]发生可遗传变化的过程 "1 ,是解释生命多样性的统一框架,指导我们理解生物过程、物种相互作用以及新医疗和生物技术创新的发展。进化生理学是一个多学科领域,探讨生物如何使其生理功能适应不断变化的环境条件。一些作者认为,进化生理学作为一门亚专业的发展或出现是在 20 世纪 80 年代末2 ,该领域综合了遗传学、生态学和进化生物学的观点,以了解生理多样性的起源、适应性和维持。被称为 "尼安德特人基因组的读者 "3 的斯万特-佩博(Svante Pääbo)可被视为开启远古基因组学大门的典范。然而,一项研究若要触及进化生理学,并不一定要把主要精力放在阐明远古时代的发展上。在本文中,我们将对近期发表的旨在研究通过自然选择产生的生理适应性和权衡的文章进行更深入的探讨,从而揭示进化的途径、结果和前景。4 索科洛娃等人的研究揭示了环境温度变化对能量代谢的影响,进而对线粒体功能的影响。线粒体通常在生物 101 课程中被介绍为细胞发电厂,其本身几乎就是进化发展的奇异范例。哺乳动物机体内的其他实体的血统也值得商榷,例如类似逆转录病毒的 Gag 蛋白 Arc1,我们不知道为什么它有一个类似逆转录病毒/逆转录转座子蛋白的结构域,这些蛋白多聚成一个包有病毒 RNA 的噬菌体。直到最近,最常见的理论是内共生假说,即细菌细胞化合物融入真核细胞。不过,最近出现的证据引发了线粒体是否真的在真核细胞之后出现,或者说这种细胞器是否与含有线粒体的细胞同时起源的问题6。然而,线粒体的细菌特性,如胞嘧啶-磷酸鸟苷、膜脂心磷脂、N-醛化肽和环状双链 DNA,可能是线粒体受损后诱发或延续炎症过程的原因:棕色脂肪组织(BAT)表达产热解偶联蛋白1(UCP1),使人类能够在寒冷应激时保持体温。最近发现成年人如何保留BAT,这可能在非颤抖性产热中发挥作用,因此有人假设BAT的可塑性是人类向环极地区扩张的主要因素。最近开发的 UCP-1 缺陷动物模型可以更仔细地观察非颤抖性产热9 和对寒冷挑战的产热适应10 ,并在 UCP-1 被发现和描述 50 年后进一步了解哺乳动物棕色脂肪(非颤抖性)产热11 的进化。12 此外,线粒体似乎在脊椎动物适应缺氧甚至缺氧环境13 的进化过程中发挥了关键作用,主要包括心肺功能14、15 和神经肌肉16 的适应。老普林尼在其《自然史》第 XXXI 卷中提到了一种盐,他将其命名为 "hammoniacum",人们认为这种盐的得名是因为它靠近位于罗马昔兰尼加省的朱庇特阿蒙神庙(希腊语为Ἄμμων Ammon)17。氨是所谓的 "氮废物 "之一,它与尿素、尿酸和肌酐一起产生于哺乳动物的蛋白质新陈代谢,必须排出体外以避免中毒。
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来源期刊
Acta Physiologica
Acta Physiologica 医学-生理学
CiteScore
11.80
自引率
15.90%
发文量
182
审稿时长
4-8 weeks
期刊介绍: Acta Physiologica is an important forum for the publication of high quality original research in physiology and related areas by authors from all over the world. Acta Physiologica is a leading journal in human/translational physiology while promoting all aspects of the science of physiology. The journal publishes full length original articles on important new observations as well as reviews and commentaries.
期刊最新文献
Chloride fluxes and GABA release sustain inhibition in the CNS: The role for Bestrophin 1 anion channels. Correction to "Beneficial effects of MGL-3196 and BAM15 combination in a mouse model of fatty liver disease". Issue Information Impaired suppression of fatty acid release by insulin is a strong predictor of reduced whole-body insulin-mediated glucose uptake and skeletal muscle insulin receptor activation. Differential production of mitochondrial reactive oxygen species between mouse (Mus musculus) and crucian carp (Carassius carassius)
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