Optogenetics is a revolutionary technique that enables noninvasive activation of electrically excitable cells. In mammals, heart rate has traditionally been modulated with pharmacological agents or direct stimulation of cardiac tissue with electrodes. However, implanted wires have been known to cause physical damage and damage from electrical currents. Here, we describe a proof of concept to optically drive cardiac function in a model organism, Drosophila melanogaster. We expressed the light sensitive channelrhodopsin protein ChR2.XXL in larval Drosophila hearts and examined light‐induced activation of cardiac tissue. After demonstrating optical stimulation of larval heart rate, the approach was tested at low temperature and low calcium levels to simulate mammalian heart transplant conditions. Optical activation of ChR2.XXL substantially increased heart rate in all conditions. We have developed a system that can be instrumental in characterizing the physiology of optogenetically controlled cardiac function with an intact heart.

Ectothermic animals are susceptible to temperature changes such as cold shock with seasons. To survive through a cold shock or season, ectotherms have developed unique strategies. Our interest is focusing on the modulation of physiological functions during cold shock and prolonged cold exposure in the fruit fly. We use Drosophila melanogaster as a model system to investigate cardiac function in response to modulators (5-HT-serotonin, Ach-acetylcholine, OA-octopamine, DA-dopamine and a cocktail of modulators) in acute cold shock and chronic cold shock conditions. Semi-intact larvae are used to provide direct access to the modulators of known concentration in a defined saline. The results show that 10 µM 5HT is the only modulator which maintains heart rate for larva raised at 21 °C and then exposed to acute cold shock (10 °C). The modulators 1 µM OA, 10 µM 5HT, 1 mM Ach, 10 µM Ach and a cocktail of modulators (at 10 µM) increased the heart rate significantly in larvae which were cold conditioned (10 °C for 10 days). HPLC analysis indicated both OA and 5-HT decreased in chronic cold conditioning. The larvae maintain heart function in the cold which may be contributed by low circulating levels of modulators. The larval heart responds better to 5-HT, OA, and Ach in conditioned cold than for acute cold, suggesting some acclimation to cold.

Proprioceptive neurons monitor the movements of limbs and joints to transduce the movements into electrical signals. These neurons function similarly in species from arthropods to humans. These neurons can be compromised in disease states and in adverse environmental conditions such as with changes in external and internal pH. We used two model preparations (the crayfish muscle receptor organ and a chordotonal organ in the limb of a crab) to characterize the responses of these proprioceptors to external and internal pH changes as well as raised CO2. The results demonstrate the proprioceptive organs are not highly sensitive to changes in extracellular pH, when reduced to 5.0 from 7.4. However, if intracellular pH is decreased by exposure to propionic acid or saline containing CO2, there is a rapid decrease in firing rate in response to joint movements. The responses recover quickly upon reintroduction of normal pH (7.4) or saline not tainted with CO2. These basic understandings may help to address the mechanistic properties of mechanosensitive receptors in other organisms, such as muscle spindles in skeletal muscles of mammals and tactile as well as pressure (i.e., blood pressure) sensory receptors. KEYWORDS: Proprioception; Sensory; Invertebrate; Carbon Dioxide; Protons; Mechanosensory; Intracellular pH; Extracellular pH

Proprioception of limbs and joints is a basic sensory function throughout most of the animal kingdom. It is important to understand how proprioceptive organs and the associated sensory neurons function with altered environments such as increased potassium ion concentrations ([K]) from diseased states, ionic imbalances, and damaged tissues. These factors can drastically alter neuronal activity. To assess this matter, we used the chordotonal organ in a walking leg of a blue crab (Callinectes sapidus) and the muscle receptor organ of the crayfish (Procambarus clarkii). These organs serve as tractable models for the analysis of proprioception. The preparations can help serve as translational models for these effects, which may be observed in other invertebrate species as well as mammalian species (including humans). When extracellular potassium concentration ([K]) is increased to 20 mM in both preparations, mixed results are observed with activity increasing in some preparations and decreasing in others after mechanical displacement. However, when [K] is increased to 40 mM, activity drastically decreases in all preparations. Additionally, proprioceptor sensory activity declines upon exposure to a diluted muscle homogenate, which contains a host of intracellular constituents. The robust effects of altered [K] on proprioception in these models illuminate the potential detriments on neuronal function in cases of severe tissue damage as well as altered [K].