Temperature alters solute transport in growth plate cartilage measured by in vivo multiphoton microscopy

• Published in: Journal of applied physiology (1985) Vol. 106; no. 6; pp. 2016 - 2025
• Main Authors: Serrat, Maria A, Williams, Rebecca M, Farnum, Cornelia E
• Format: Journal Article
• Language: English
• Published: Bethesda, MD Am Physiological Soc 01.06.2009; American Physiological Society
• Subjects: Animals; Biological and medical sciences; Bone Development - physiology; Bones; Cartilage; Cold Temperature; Female; Fluorescein - administration & dosage; Fluorescence; Fundamental and applied biological sciences. Psychology; Growth Plate - physiology; Hindlimb; Hot Temperature; Innovative Methodology; Lasers; Male; Mice; Microscopy; Microscopy - methods; Microscopy, Fluorescence - methods; Oxytetracycline; Photons; Physiology; Rodents; Temperature; Tibia - growth & development; Temperature; Chondrocyte; Growth; Biological transport; nutrient supply; Solutes; bone elongation; Blood flow; Osteoarticular system; Cartilage; In vivo; Vertebrata; Mammalia; Extracellular matrix; Nutrient; Hemodynamics; Bone; Elongation
• ISSN: 8750-7587; 1522-1601
• DOI: 10.1152/japplphysiol.00295.2009

1 Department of Biomedical Sciences and 2 Department of Biomedical Engineering, Cornell University, Ithaca, New York Submitted 19 March 2009 ; accepted in final form 13 April 2009 Solute delivery to avascular cartilaginous plates is critical to bone elongation, and impaired transport of nutrients and growth factors in cartilage matrix could underlie many skeletal abnormalities. Advances in imaging technology have revolutionized our ability to visualize growth plates in vivo, but quantitative methods are still needed. We developed analytical standards for measuring solute delivery, defined by amount and rate of intravenous tracer entry, in murine growth plates using multiphoton microscopy. We employed an acute temperature model because of its well-established impact on bone circulation and tested the hypothesis that solute delivery changes positively with limb temperature when body core and respiration are held constant (36°C, 120 breaths/min). Tibial growth plates were surgically exposed in anesthetized 5-wk-old mice, and their hindlimbs were immersed in warm (36°C) or cool (23°C) saline ( n = 6/group). After 30 min of thermal equilibration, we administered an intracardiac injection of fluorescein (50 µl, 0.5%) and captured sequentially timed growth plate images spanning 10 min at standardized depth. Absolute growth plate fluorescence was normalized to vascular concentrations for interanimal comparisons. As predicted, more fluorescein infiltrated growth plates at 36°C, with standardized values nearly double those at 23°C. Changing initial limb temperature did not alter baseline values, suggesting a sustained response period. These data validate the sensitivity of our system and have relevance to strategies for enhancing localized delivery of therapeutic agents to growth plates of children. Applications of this technique include assessment of solute transport in models of growth plate dysfunction, particularly chondrodysplasias with matrix irregularities. bone elongation; chondrocyte; extracellular matrix; nutrient supply; blood flow Address for reprint requests and other correspondence: M. A. Serrat, Cornell Univ., Dept. of Biomedical Sciences, T5-002 Vet Research Tower, Ithaca, NY 14853-6401 (e-mail: maria.a.serrat{at}gmail.com )