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Swimming stamina in adult fish is heritable, it is unknown if inherited traits that support enhanced swimming stamina in offspring appear only in juveniles and/or adults, or if these traits actually appear earlier in the morphologically quite different larvae. To answer this question, mature adult zebrafish (Danio rerio) were subjected to a swimming performance test that allowed separation into low swimming stamina or high swimming stamina groups. Adults were then bred within their own performance groups. Larval offspring from each of the two groups, designated high (LHSD) and low stamina-derived larvae (LLSD), were then reared at 27°C in aerated water (21% O2). Routine (fH,r) and active (fH,a) heart rate, and routine (M.O2,r) and active (M.O2,a) mass-specific oxygen consumption were recorded from 5 days post fertilization (dpf) through 21 dpf, and gross cost of transport and factorial aerobic metabolic scope were derived from M.O2 measurements. Heart rate generally ranged between 150 and 225 b•min-1 in both LHSD and LLSD populations. However, significant (P

This study was planned to determine the cardiovascular effects of sāvitrī prāņāyāma, a rhythmical, slow and deep breathing technique done in sitting and supine positions. Heart rate, systolic and diastolic blood pressureĀ were recorded in 11 female subjects before and after 5 minutes of normal breathing and sāvitrī in sitting and supine positions. Overall comparisons of Δ% changes following sāvitrī and normal breathing in both sitting and supine positions revealed significant difference betvveen groups with regard to heart rate, diastolic, mean pressure, rate-pressure product and double product. In sitting positions the Δ% was lower following sāvitrī whereas in supine position the Δ% was higher following sāvitrī. It is concluded that the practice of sāvitrī in sitting position has beneficial cardiovascular effects. [ABSTRACT FROM AUTHOR]

Swimming stamina in adult fish is heritable, it is unknown if inherited traits that support enhanced swimming stamina in offspring appear only in juveniles and/or adults, or if these traits actually appear earlier in the morphologically quite different larvae. To answer this question, mature adult zebrafish (Danio rerio) were subjected to a swimming performance test that allowed separation into low swimming stamina or high swimming stamina groups. Adults were then bred within their own performance groups. Larval offspring from each of the two groups, designated high (L(HSD)) and low stamina-derived larvae (L(LSD)), were then reared at 27°C in aerated water (21% O(2)). Routine (f(H),r) and active (f(H),a) heart rate, and routine [Formula: see text] and active [Formula: see text] mass-specific oxygen consumption were recorded from 5 days post fertilization (dpf) through 21 dpf, and gross cost of transport and factorial aerobic metabolic scope were derived from [Formula: see text] measurements. Heart rate generally ranged between 150 and 225 bpm in both L(HSD) and L(LSD) populations. However, significant (P < 0.05) differences existed between the L(LSD) and L(HSD) populations at 5 and 14 dpf in f(H),r and at days 10 and 15 dpf in f(H),a. [Formula: see text] was 0.04-0.32 μmol mg(-1) h(-1), while [Formula: see text] was 0.2-1.2 μmol mg(-1) h(-1). Significant (P < 0.05) differences between the L(LSD) and L(HSD) populations in [Formula: see text] occurred at 7, 10, and 21 dpf and in [Formula: see text] at 7 dpf. Gross cost of transport was ∼6-10 μmol O(2)·μg(-1) m(-1) at 5 dpf, peaking at 14-19 μmol O(2) μg(-1) m(-1) at 7-10 dpf, before falling again to 5-6 μmol O(2) μg(-1) m(-1) at 21 dpf, with gross cost of transport significantly higher in the L(LSD) population at 7 dpf. Collectively, these data indicate that inherited physiological differences known to contribute to enhanced stamina in adult parents also appear in their larval offspring well before attainment of juvenile or adult features.