de Souza Silvia Cristina R, Kuribara Claudia M
Departamento de Fisiologia, Instituto de Biociências, Universidade de São Paulo, Rua do Matão, Travessa 14, n 321, Cidade Universitária, CEP 05508-900, São Paulo, SP, Brazil.
J Exp Biol. 2006 May;209(Pt 9):1651-61. doi: 10.1242/jeb.02195.
The early larvae of P. paradoxus grow large but metamorphose into relatively small frogs, the diminished post-metamorphic growth producing a marked contrast between maximum larval size and adult. Thus, O(2) uptake does not appear to limit the energy expenditure on growth processes, and unlike in other anuran larvae, may not be a surface area-related function in P. paradoxus larvae. The resting rates of metabolism (M(O(2))) and partitioning between aquatic (Mw(O(2))) and aerial O(2) uptake (Ma(O(2))) were measured on tadpoles and froglets by closed system respirometry, using water of P(O(2)) ranging from 145 to 40 mmHg. Correlative changes in body glycogen and lactate were examined by standard enzyme assays. Scaling patterns in the growth and degrowth stages were analysed on whole-body, log-transformed data using linear regressions. In normoxia, M(O(2)) was 2.1-2.5 mumol g(-1) h(-1) in the early larvae, increasing more than twofold on forelimb emergence and decreasing sharply in the froglets; M(O(2)) varies in strict proportion to body mass (M(b)), both in the growth (b=1.02) and degrowth (b=0.97) phases, according to the equation M(O(2))=aM(b)(b), where b is the scaling coefficient. Mw(O(2)) constitutes >90% of total uptake in the growth stages, increasing with b=1.02 while Ma(O(2)) increases with b=1.13; during degrowth there is a change in the pattern related to intensification of metamorphosis. Hypoxic water did not affect M(O(2)); however, in all larval stages Mw(O(2)) and Ma(O(2)) changed with a decrease in P(O(2)). At 60 mmHg, rates are more severely affected in the largest tadpoles, causing the b values for Mw(O(2)) and Ma(O(2)) to change to 0.11 and 1.44, respectively, in the growth phase. Glycogen and lactate levels increase out of proportion with body mass increase (b=2.05 and 1.47, respectively) in the growth stages, and increase anaerobic capacity in late metamorphosis. In hypoxic water, glycogen levels decrease in the growth stages and the largest tadpoles accumulate surplus lactate, possibly related to surfacing activity. Our results may reveal the consequences of size on energy demand at the tissue level in P. paradoxus larvae, indicating that air breathing must subsidise energy expenditure during larval development.
奇异多指节蟾的早期幼体长得很大,但变态后变成相对较小的青蛙,变态后生长的减少使得最大幼体大小与成体之间形成了显著差异。因此,氧气摄取似乎并不限制生长过程中的能量消耗,与其他无尾类幼体不同,奇异多指节蟾幼体的氧气摄取可能与表面积无关。通过封闭系统呼吸测定法,使用氧分压(P(O₂))范围为145至40 mmHg的水,测量了蝌蚪和幼蛙的静息代谢率(M(O₂))以及水生(Mw(O₂))和空气氧气摄取(Ma(O₂))之间的分配情况。通过标准酶法检测了身体糖原和乳酸的相关变化。使用线性回归对全身对数转换后的数据进行分析,以研究生长和退化阶段的标度模式。在常氧条件下,早期幼体的M(O₂)为2.1 - 2.5 μmol g⁻¹ h⁻¹,在前肢出现时增加两倍多,在幼蛙中急剧下降;根据方程M(O₂)=aM(b)(b),其中b是标度系数,M(O₂)在生长阶段(b = 1.02)和退化阶段(b = 0.97)均与体重(M(b))严格成比例变化。Mw(O₂)在生长阶段占总摄取量的90%以上,随b = 1.02增加,而Ma(O₂)随b = 1.13增加;在退化阶段,与变态加剧相关的模式发生了变化。缺氧水不会影响M(O₂);然而,在所有幼体阶段,Mw(O₂)和Ma(O₂)随P(O₂)的降低而变化。在60 mmHg时,最大的蝌蚪的摄取率受到更严重的影响,导致生长阶段Mw(O₂)和Ma(O₂)的b值分别变为0.11和1.44。在生长阶段,糖原和乳酸水平的增加与体重增加不成比例(分别为b = 2.05和1.47),并且在变态后期增加了无氧能力。在缺氧水中,生长阶段糖原水平下降,最大的蝌蚪积累了多余的乳酸,这可能与浮出水面的活动有关。我们的结果可能揭示了奇异多指节蟾幼体在组织水平上大小对能量需求的影响,表明空气呼吸必须在幼体发育过程中补贴能量消耗。