Improved knowledge on the swimming physiology of fish and its application to fisheries science and aquaculture (i.e., farming a fitter fish) is currently needed in the face of global environmental changes, high fishing pressures, increased aquaculture production as well as increased concern on fish well-being. Here, we review existing data on teleost fish that indicate that sustained exercise at optimal speeds enhances muscle growth and has consequences for flesh quality. Potential added benefits of sustained exercise may be delay of ovarian development and stimulation of immune status. Exercise could represent a natural, noninvasive, and economical approach to improve growth, flesh quality as well as welfare of aquacultured fish: a FitFish for a healthy consumer. All these issues are important for setting directions for policy decisions and future studies in this area. For this purpose, the FitFish workshop on the Swimming Physiology of Fish (http://www.ub.edu/fitfish2010) was organized to bring together a multidisciplinary group of scientists using exercise models, industrial partners, and policy makers. Sixteen international experts from Europe, North America, and Japan were invited to present their work and view on migration of fishes in their natural environment, beneficial effects of exercise, and applications for sustainable aquaculture. Eighty-eight participants from 19 different countries contributed through a poster session and round table discussion. Eight papers from invited speakers at the workshop have been contributed to this special issue on The Swimming Physiology of Fish.

Zebrafish has been largely accepted as a vertebrate multidisciplinary model but its usefulness as a model for exercise physiology has been hampered by the scarce knowledge on its swimming economy, optimal swimming speeds and cost of transport. Therefore, we have performed individual and group-wise swimming experiments to quantify swimming economy and to demonstrate the exercise effects on growth in adult zebrafish. Individual zebrafish (n = 10) were able to swim at a critical swimming speed (U_crit) of 0.548±0.007 m s⁻¹ or 18.0 standard body lengths (BL) s⁻¹. The optimal swimming speed (U_opt) at which energetic efficiency is highest was 0.396±0.019 m s⁻¹ (13.0 BL s⁻¹) corresponding to 72.26±0.29% of U_crit. The cost of transport at optimal swimming speed (COT_opt) was 25.23±4.03 µmol g⁻¹ m⁻¹. A group-wise experiment was conducted with zebrafish (n = 83) swimming at U_opt for 6 h day⁻¹ for 5 days week⁻¹ for 4 weeks vs. zebrafish (n = 84) that rested during this period. Swimming zebrafish increased their total body length by 5.6% and body weight by 41.1% as compared to resting fish. For the first time, a highly significant exercise-induced growth is demonstrated in adult zebrafish. Expression analysis of a set of muscle growth marker genes revealed clear regulatory roles in relation to swimming-enhanced growth for genes such as growth hormone receptor b (ghrb), insulin-like growth factor 1 receptor a (igf1ra), troponin C (stnnc), slow myosin heavy chain 1 (smyhc1), troponin I2 (tnni2), myosin heavy polypeptide 2 (myhz2) and myostatin (mstnb). From the results of our study we can conclude that zebrafish can be used as an exercise model for enhanced growth, with implications in basic, biomedical and applied sciences, such as aquaculture.

Previous studies from our laboratory have shown that salmon gonadotropins GTH I and GTH II have similar effects on testicular steroidogenesis in vitro. To determine whether the relative potencies of GTH I and GTH II changed during late stages of spermatogenesis, the effects of GTH I and GTH II on in vitro steroid production by testicular tissue from fish in stages IV to V of spermatogenesis were examined. Fragments of testicular tissue were incubated with GTH I and GTH II for 18 h at 15 degrees C. The in vitro production of 11-ketotestosterone (11-KT), testosterone (T), 17 alpha-hydroxyprogesterone (17OH-P), and 17 alpha,20 beta-dihydroxy-4-pregnen-3-one (17,20 beta-P) was determined by RIA. GTH I and GTH II were equipotent in stimulating the production of 11-KT, T, and 17,20 beta-P (17OH-P was not detectable) by testicular tissue in stage IV of spermatogenesis. The sensitivity of testicular tissue to the steroidogenic effects of GTH II increased as spermatogenesis progressed. In contrast, the sensitivity of testicular tissue to the effects of GTH I on 17,20 beta-P production declined from stages IV to V, while the sensitivity of testicular tissue to the effects of GTH I on 11-KT production remained unchanged. These changes in sensitivity to GTH I and II are consistent with previously reported changes in GTH receptors in salmon testis and support the hypothesis that GTH I and GTH II may have different roles during spermatogenesis.