Comprehensive expression analysis of hormone-like substances in the subcutaneous adipose tissue of the common bottlenose dolphin Tursiops truncatus.

Marine mammals possess a specific subcutaneous fat layer called blubber that not only insulates and stores energy but also secretes bioactive substances. However, our understanding of its role as a secretory organ in cetaceans is incomplete. To exhaustively explore the hormone-like substances produced in dolphin subcutaneous adipose tissue, we performed seasonal blubber biopsies from captive female common bottlenose dolphins (Tursiops truncatus; N = 8, n = 32) and analyzed gene expression via transcriptomics.

Association of seasonal changes in circulating cortisol concentrations with the expression of cortisol biosynthetic enzymes and a glucocorticoid receptor in the blubber of common bottlenose dolphin.

Cortisol is secreted from the adrenal cortex in response to stress, and its circulating levels are used as robust physiological indicators of stress intensity in various animals. Cortisol is also produced locally in adipose tissue by the conversion of steroid hormones such as cortisone, which is related to fat accumulation. Circulating cortisol levels, probably induced by cold stress, increase in cetaceans under cold conditions.

Blubber biopsy in common bottlenose dolphins using a novel biopsy puncher: Evaluation of the impact on living individuals and possibility of applications in cetacean research.

Biopsy has recently become a preferred protocol for sampling the skin and blubber of many cetacean species, although it is desirable to collect as minimally invasive as possible. Here, the effect of biopsy sampling on the captive common bottlenose dolphins was evaluated by analyzing the process of wound healing and changes in hematological and blood biochemical parameters after biopsy using a puncher developed to collect up to the inner layer of the dolphin blubber. Results showed that the wounds caused by biopsy were closed in as early as 1 day and completely covered with the epidermis within 5-11 days.

Luminescent Thermoresponse via Excimer/Exciplex Transition of Pyrene Derivative in Polymer Networks Containing [3]Rotaxane.

The modulation of molecular interaction with a [3]rotaxane structure enabled a luminescent thermoresponse with high sensitivity over a wide temperature range. Herein, a pyrene moiety was encapsulated by permethylated α-cyclodextrins and was introduced into a polymer network material of poly(vinyl alcohol) as a cross-linker. The luminescence nature associated with the pyrene moiety was continuously switched from a static pyrene-pyrene excimer emission mode at 193 K to a dynamic pyrene-dimethylaniline (DMA) exciplex emission mode at 293 K.

Towards non-invasive heart rate monitoring in free-ranging cetaceans: a unipolar suction cup tag measured the heart rate of trained Risso's dolphins.

Heart rate monitoring in free-ranging cetaceans to understand their behavioural ecology and diving physiology is challenging. Here, we developed a simple, non-invasive method to monitor the heart rate of cetaceans in the field using an electrocardiogram-measuring device and a single suction cup equipped with an electrode. The unipolar suction cup was placed on the left lateral body surface behind the pectoral fin of Risso's dolphins () and a false killer whale () in captivity; their heart rate was successfully monitored.

Macroscopic Change in Luminescent Color by Thermally Driven Sliding Motion in [3]Rotaxanes.

Systematic investigation of rotaxane structures has revealed a rational design for thermally driven switching of their macroscopic properties. At low temperature, the luminophore is insulated by the macrocycles and displays monomer emission, whereas at high temperature, the luminophore is exposed owing to a change in the macrocyclic location distribution and interacts with external molecules, affording a thermally driven luminescent color change with high reversibility and responsiveness. This macroscopic switching through efficient thermal sliding was made possible by appropriate tuning of both the macrocycle-luminophore interactions within the rotaxane and the coupling between the excited luminophore and external molecules in an exciplex.