普通滇金丝猴(Tenrec ecaudatus)在缺氧和高碳酸血症时会减少耗氧量,但体温和心率不会发生同步变化。

IF 1.7 3区 生物学 Q4 PHYSIOLOGY Journal of Comparative Physiology B-Biochemical Systems and Environmental Physiology Pub Date : 2024-12-01 Epub Date: 2024-10-07 DOI:10.1007/s00360-024-01587-9
Claudia Silva Rubio, Anne B Kim, William K Milsom, Matthew E Pamenter, Gilbecca Rae Smith, Frank van Breukelen
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引用次数: 0

摘要

普通箭猪(Tenrec ecaudatus)是一种穴居哺乳动物,在马达加斯加及其邻近岛屿的活动和冬眠季节都使用洞穴。人们普遍认为恬莱鼠的个体冬眠期为 8-9 个月,但我们从距离地表 1 米深的同一密封洞穴中取出了 13 只恬莱鼠。这种在密封洞穴中的集体冬眠可能会造成缺氧和/或高碳酸环境,并表明这种有胎盘的哺乳动物可能对缺氧和高碳酸环境的耐受性更强。为了确定天牛的情况是否如此,我们让天牛在低温(16 °C)或高温(28 °C)环境下(Ta)暴露于急性缺氧(4 小时 16% 或 7% 的氧气)、渐进性缺氧(2 小时 16%、10% 和 4% 的氧气)或渐进性高碳酸血症(2 小时 2%、5% 和 10% 的二氧化碳)。此外,还在 10、25 和 37 °C条件下构建了腱鱼全血的氧平衡曲线,以确定血红蛋白(Hb)-O2 亲和力是否有助于耐缺氧性。在 16 °C的动物中,正常缺氧和正常碳酸血症水平下的耗氧率(V ˙ O 2)、体温(Tb)和心率(HR)在个体间存在很大差异。在 28 °C条件下,动物耗氧量和体温的个体间差异大大降低。缺氧(急性和进行性)和进行性高碳酸血症都会导致 V ˙ O 2 的下降,以及在 16 °C条件下动物之间 V ˙ O 2 的差异。在 7% O2 条件下,16 °C条件下滇金丝猴的耗氧率下降与体温变化无关,这种情况是独特的,与其他冬眠物种典型的缺氧代谢反应(取决于 Tb 的同时下降)不一致。在 28 °C下的动物,暴露于低至 4% 的氧气水平和高至 10% 的二氧化碳水平对 V ˙ O 2、心率或 Tb 没有显著影响,这表明它们对缺氧和高碳酸血症都有很高的耐受性。在所有气体成分和温度条件下,不同个体之间的心率仍存在很大差异。Tenrec的Hb-O2亲和力与其他胎盘哺乳动物相似,可能不会导致缺氧耐受性的提高。最终,我们的研究结果表明,Ta的变化决定了tenrecs对低氧或高碳酸血症的生理反应,这种反应是爬行动物的特征,而不是大多数胎盘哺乳动物的特征。鉴于鼩鼱的许多解剖学和生理学特征表明它们可能是祖先胎盘哺乳动物的代表,我们的研究结果表明典型的低氧代谢反应是在哺乳动物进化的后期演化而来的。
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Common tenrecs (Tenrec ecaudatus) reduce oxygen consumption in hypoxia and in hypercapnia without concordant changes to body temperature or heart rate.

Common tenrecs (Tenrec ecaudatus) are fossorial mammals that use burrows during both active and hibernating seasons in Madagascar and its neighboring islands. Prevailing thought was that tenrecs hibernate for 8-9 months individually, but 13 tenrecs were removed from the same sealed burrow 1 m deep from the surface. Such group hibernation in sealed burrows presumably creates a hypoxic and/or hypercapnic environment and suggests that this placental mammal may have an increased tolerance to hypoxia and hypercapnia. Higher tolerances to hypoxia and hypercapnia have been documented for other mammals capable of hibernation and to determine if this is the case for tenrecs, we exposed them to acute hypoxia (4 h of 16 or 7% O2), progressive hypoxia (2 h of 16, 10 and 4% O2), or progressive hypercapnia (2 h of 2, 5 and 10% CO2) at cold (16 °C) or warm (28 °C) ambient temperatures (Ta). Oxygen equilibrium curves were also constructed on the whole blood of tenrecs at 10, 25, and 37 °C to determine if hemoglobin (Hb)-O2 affinity contributes to hypoxia tolerance. In animals held at 16 °C, normoxic and normocapnic levels of oxygen consumption rate ( V ˙ O 2 ), body temperature (Tb), and heart rate (HR) were highly variable between individuals. This inter-individual variation was greatly reduced in animals held at 28 °C for oxygen consumption rate and body temperature. Both hypoxia (acute and progressive) and progressive hypercapnia led to decreases in V ˙ O 2 as well as the variation in V ˙ O 2 between animals held at 16 °C. The fall in oxygen consumption rate in 7% O2 independent of changes in body temperature in tenrecs held at 16 °C is unique and not consistent with the typical hypoxic metabolic response seen in other hibernating species that depends on concomitant falls in Tb. In animals held at 28 °C, exposure to O2 levels as low as 4% and CO2 levels as high as 10% had no significant effect on V ˙ O 2 , HR, or Tb, indicative of high tolerance to both hypoxia and hypercapnia. High variation in heart rate remained between individuals in all gas compositions and at all temperatures. Tenrec Hb-O2 affinity was similar to other homeothermic placental mammals and likely does not contribute to the increased hypoxia tolerance. Ultimately, our results suggest changes in Ta dictate physiological responses to hypoxia or hypercapnia in tenrecs, responses more characteristic of reptiles than of most placental mammals. Given that numerous anatomical and physiological characteristics of tenrecs suggest that they may be representative of an ancestral placental mammal, our findings suggest the typical hypoxic metabolic response evolved later in mammalian evolution.

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来源期刊
CiteScore
3.90
自引率
0.00%
发文量
51
审稿时长
3.5 months
期刊介绍: The Journal of Comparative Physiology B publishes peer-reviewed original articles and reviews on the comparative physiology of invertebrate and vertebrate animals. Special emphasis is placed on integrative studies that elucidate mechanisms at the whole-animal, organ, tissue, cellular and/or molecular levels. Review papers report on the current state of knowledge in an area of comparative physiology, and directions in which future research is needed.
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