A Rabbit Model for Prolonged Continuous Intravenous Infusion Via a Peripherally Inserted Central Catheter

Medical treatment may require the continuous intravenous (IV) infusion of drugs to sustain the therapeutic blood concentration and to minimize dosing errors. Animal disease models that ultimately mimic the intended use of new potential drugs via a continuous IV infusion in unrestrained, free roaming animals are required. While peripherally inserted central catheters (PICCs) and other central line techniques for prolonged IV infusion of drugs are prevalent in the clinic, continuous IV infusion methods in an animal model are challenging and limited. In most cases, continuous IV infusion methods require surgical knowledge as well as expensive and complicated equipment. In the current work, we established a novel rabbit model for prolonged continuous IV infusion by inserting a PICC line from the marginal ear vein to the superior vena cava and connecting it to an externally carried ambulatory infusion pump. Either saline or a clinically relevant formulation could be steadily and continuously infused at 3–6 ml/h for 11 consecutive days into freely moving rabbits while maintaining normal body temperature, weight, and respiration physiology, as determined by daily spirometry. This new model is simple to execute and can advance the ability to administer and test new drug candidates.

Gas Exchange Gamified: Teaching Respiration Physiology with a Novel Board Game

Pulmonary gas exchange is a complex component of respiratory physiology. For many students, the movement of unseen gases can seem abstract and confusing. The “Gas Exchange Game” is a novel board game designed for use in a second-semester anatomy and physiology course. Students apply textbook knowledge of the laws of gas exchange and use the game board and pieces to see concrete examples of how gases move in the human body.

Pulmo uterinus: a history of ideas on fetal respiration

Theories about fetal respiration began in antiquity. Aristotle characterized pneuma as warm air, but also as the enabler of vital functions and instrument of the soul. In Galen’s system of physiology, the vital spirit was carried by the umbilical arteries, the nutrients by the umbilical vein from the placenta to the fetus. In 1569 Aranzio postulated that the maternal and fetal vasculatures are distinct. From 1670 to 1690, a century before the discovery of oxygen, researchers understood that during respiration some form of exchange with the air must occur, naming the substance biolychnium, phlogiston, sal-nitro, or nitro-aerial particles. An analogy of placental and pulmonary gas exchange was described in 1674 by Mayow. In 1779, Lavoisier understood the discovery of oxygen, discarded the phlogiston theory, and based respiration physiology on gas exchange. With the invention of the spectroscope, it became possible to measure hemoglobin oxygenation, and in 1876 Zweifel proved fetal oxygen uptake. Major progress in understanding fetal gas exchange was achieved in the 20th century by the physiologists Barcroft in Cambridge and Dawes in Oxford.

The oxygen consumption rates of different life stages of the endoparasitic nematode

The oxygen consumption rates of different life stages of the endoparasitic nematode, Pratylenchus zeae (Nematoda: Tylenchida) during non- and post-anhydrobiosisPratylenchus zeae, widely distributed in tropical and subtropical regions, is an endoparasite in roots of maize and other crop plants. The nematode is attracted to plant roots by CO2 and root exudates and feeds primarily on cells of the root cortex, making channels and openings where the eggs are deposited, with the result that secondary infection occurs due to bacteria and fungi. Nothing is known about the respiration physiology of this nematode and how it manages to survive during dry seasons. To measure the oxygen consumption rate (VO2 ) of individual P. zeae (less than half a millimeter long), a special measuring technique namely Cartesian diver micro-respirometry was applied. The Cartesian divers were machined from Perspex, and proved to be more accurate to measure VO2 compared with heavier glass divers used in similar experiments on free living nematodes. An accuracy of better than one nanoliter of oxygen consumed per hour was achieved with a single P. zeae inside the diver. Cartesian diver micro-respirometry measurements are based in principle on the manometric changes that occur in a fl otation tube in a manometer set-up when oxygen is consumed by P. zeae and CO2 from the animal is chemically absorbed. VO2 was measured for eggs (length: < 0.05 mm), larvae (length: 0.36 mm) and adults (length: 0.47 mm) before induction to anhydrobiosis. P. zeae from infected maize roots were extracted and exposed aseptically to in vitro maize root cultures in a grow cabinet at 50 % to 60% relative humidity at 28 ºC using eggs, larvae and adults. VO2 was also measured for post-anhydrobiotic eggs, larvae and adults by taking 50 individuals, eggs and larvae from the culture and placing them in Petri-dishes with 1% agar/water to dry out for 11 days at 28 ºC and 50% relative humidity. The VO2 was measured after the anhydrobiotic eggs, larvae and adults were re-hydrated for 12 hours in a high humidity atmosphere. The average VO2 value found for ten consecutive measurements during a 50 minute period of one adult using the diver technique was 32.8 nanoliter per hour. The differences between the ten VO2 values were less than 3.5 %, an indication of the accuracy of the diver measurements. The average VO2 values from ten measurements per life stage, expressed in nanolitres per hour per life stage of the pre-anhydro-biotes (eggs: 7.96; larva: 6.13; adult: 26.04) were compared with those of post-anhydrobiotes 12 hours after anhydrobiosis. The average VO2 values of the post-anhydrobiotes for the three life stages (egg: 19.34; larva: 14.17; adult: 32.86) were statistically signifi cantly higher in comparison with the pre-anhydrobiotes. The reasons for the difference are that high concentrations of metabolites, probably in the form of trehalose, accumulate during the anhydrobiosis stage to be utilized during the post-anhydrobiotic revival period. The oxygen consumption rate was also expressed in nanolitres per hour per microgram adult nematode after applying the following equation taken from the literature: M = a2 x b/16 x 1000 where M = mass (µg) of adult nematode; a = largest body width (µm); b = body length (µm). Using this equation it was found that one gram P. zeae uses 503 times more oxygen compared with one gram mammal the size of a cow. This high specifi c oxygen consumption rate (MO2 ) is a direct indication of the large metabolic damage this endoparasitic nematode can have on the metabolic substrates provided by the roots of the various plant crops it parasitize.