The Role of Extracellular Fluid on the Electrical and Electromechanical Properties of Bone: A Review

1987 ◽  
Vol 110 ◽  
Author(s):  
Dennis A. Chakkalakal

The cells in living bone – osteocytes, osteoblasts and osteoclasts – are embedded in a porous material consisting of an organic-inorganic composite solid containing a distribution of fixed charges, permeated by ionic fluids flowing through a complex network of channels. In the weight-bearing long bones of the body, the largest of these channels are up to a few hundred microns in diameter and contain blood vessels which are connected to the blood supply in the central canal of the long bones. These channels establish fluid connectivity with the cells (osteocytes) responsible for maintenance of the bone tissue through small canals (canaliculi) with diameters ranging down to a tenth of a micron. Outside the blood vessels, perivascular fluid permeates these channels. The solid matrix is itself porous with a high degree of composite material organization beginning at the macromolecular level. The internal connectivity of the pore fraction of the solid, which is not as extensive as the network of channels, and the connectivity of this pore fraction with the fluid channels may affect physiological functions, through its influence on mechanical, electrical and electromechanical properties of the extracellular matrix. It seems apparent that the structure and physical properties of the extracellular material of bone will largely determine the physicochemical environment of the cells. Thus, a materials characterization of the extracellular matrix of living bone has become an essential part of the efforts to advance our knowledge of bone physiology and pathology. This paper is a review of the present state of knowledge of the electrical and electromechanical properties of this material with emphasis on studies that appear to have the most physiological significance.

Impact ◽  
2019 ◽  
Vol 2019 (8) ◽  
pp. 18-20
Author(s):  
Shuhei Tsuchiya

Osseointegration can be defined as a direct connection, both structural and functional, between living bone and the surface of an artificial implant. Indeed, the word comes from the Greek term for 'bone' and 'to make whole'. In dentistry, once dental implants are placed, the body will react with osseointegration, enabling the implants to become a permanent part of the jaw. There are many benefits to this type of implant, compared with traditional tooth replacement options, not least that dental implants mimic the strength and functionality of a natural tooth. Dr Shuhei Tsuchiya is a researcher based in the Division of Oral and Maxillofacial Surgery at Nagoya University, Japan, who is interested in a range of areas, including regenerative medicine and the extracellular matrix. One of his key preoccupations, though, is shedding light on osseointegration. He and his team are working to unravel the mysteries of the mechanism.


1989 ◽  
Vol 4 (4) ◽  
pp. 1034-1046 ◽  
Author(s):  
Dennis A. Chakkalakal

The cells in living bone are embedded in a charged, organic-inorganic solid permeated by ionic fluids flowing through a complex network of channels (diameter ∼10−1–102 μm). The solid matrix, which has a high degree of composite material organization beginning at the macromolecular level, has even finer pores of diameter ≳10−3 μm containing extracellular fluids. Since bone cells are thus bathed in fluid environments of varying ionic composition and concentration, it is likely that the physiology of bone depends on its electrical and electromechanical properties. This hypothesis is supported by the known effects of externally applied mechanical and electrical signals on physiological functions. Contrary to the earlier perception of bone as an insulating material, it is now recognized that the fluid content of bone endows it with physiologically significant conductivity. Mechanoelectric transduction in bone, at low frequencies, is most likely an electrokinetic process associated with the solid-fluid interfaces in bone. Electromechanical properties of bone have been determined experimentally by measurements of stress-generated potentials and streaming potentials in wet bone specimens and electrophoretic mobility of bone particles. Interpretation of results has been difficult due to the complexity of the solid-fluid interfaces in bone and the often undefinable alterations of the pores and interfaces due to specimen preparation. This paper is a review of the present state of knowledge of mechanoelectric transduction in bone and its physiological significance.


2018 ◽  
Vol 6 (9) ◽  
Author(s):  
DR.MATHEW GEORGE ◽  
DR.LINCY JOSEPH ◽  
MRS.DEEPTHI MATHEW ◽  
ALISHA MARIA SHAJI ◽  
BIJI JOSEPH ◽  
...  

Blood pressure is the force of blood pushing against blood vessel walls as the heart pumps out blood, and high blood pressure, also called hypertension, is an increase in the amount of force that blood places on blood vessels as it moves through the body. Factors that can increase this force include higher blood volume due to extra fluid in the blood and blood vessels that are narrow, stiff, or clogged(1). High blood pressure can damage blood vessels in the kidneys, reducing their ability to work properly. When the force of blood flow is high, blood vessels stretch so blood flows more easily. Eventually, this stretching scars and weakens blood vessels throughout the body, including those in the kidneys.


Impact ◽  
2018 ◽  
Vol 2018 (3) ◽  
pp. 26-28
Author(s):  
Jonathan Dawson ◽  
Richard Oreffo

Gels made from clay could provide an environment able to stimulate stem-cells due to their ability to bind biological molecules. That molecules stick to clay has been known by scientists since the 1960s. Doctors observed that absorption into the blood stream of certain drugs was severely reduced when patients were also receiving clay-based antacid or anti-diarrhoeal treatments. This curious phenomenon was realized to be due to binding of the drugs by clay particles. This interaction is now routinely harnessed in the design of tablets to carefully control the release and action of a drug. Dr Dawson now proposes to use this property of clay to create micro-environments that could stimulate stem cells to regenerate damaged tissues such as bone, cartilage or skin. The rich electrostatic properties of nano (1 millionth of a millimetre) -scale clay particles which mediate these interactions could allow two hurdles facing the development of stem-cell based regenerative therapies to be overcome simultaneously. The first challenge - to deliver and hold stem cells at the right location in the body - is met by the ability of clays to self-organise into gels via the electrostatic interactions of the particles with each other. Cells mixed with a low concentration (less than 4%) of clay particles can be injected into the body and held in the right place by the gel, eliminating, in many situations, the need for surgery. Clay particles can also interact with large structural molecules (polymers) which are frequently used in the development of materials (or 'scaffolds'), designed to host stem cells. These interactions can greatly improve the strength of such structures and could be applied to preserve their stability at the site of injury until regeneration is complete. While several gels and scaffold materials have been designed to deliver and hold stem cells at the site of regeneration, the ability of clay nanoparticles to overcome a second critical hurdle facing stem-cell therapy is what makes them especially exciting. Essential to directing the activity of stem-cells is the carefully controlled provision of key biological signalling molecules. However, the open structures of conventional scaffolds or gels, while essential for the diffusion of nutrients to the cells, means their ability to hold the signalling molecules in the same location as the cells is limited. The ability of clay nano-particles to bind biological molecules presents a unique opportunity to create local environments at a site of injury or disease that can stimulate and control stem-cell driven repair. Dr Dawson's early studies investigated the ability of clay gels to stimulate the growth of new blood vessels by incorporating a key molecular signal that stimulates this process, vascular endothelial growth factor (VEGF). In a manner reminiscent of the observations made in the 60s, Dr Dawson and colleagues observed that adding a drop of clay gel to a solution containing VEGF caused, after a few hours, the disappearance of VEGF from the solution as it became bound to the gel. When placed in an experimental injury model, the gel-bound VEGF stimulated a cluster of new blood vessels to form. These exciting results indicate the potential of clay nanoparticles to create tailor-made micro-environments to foster stem cell regeneration. Dr Dawson is developing this approach as a means of first exploring the biological signals necessary to successfully control stem cell behaviour for regeneration and then, using the same approach, to provide stem cells with these signals to stimulate regeneration in the body. The project will seek to test this approach to regenerate bone lost to cancer or hip replacement failure. If successful the same technology may be applied to harness stem cells for the treatment of a whole host of different scenarios, from burn victims to those suffering with diabetes or Parkinson's.


2021 ◽  
Vol 4 (1) ◽  
Author(s):  
Lei Qin ◽  
Xuekun Fu ◽  
Jing Ma ◽  
Manxia Lin ◽  
Peijun Zhang ◽  
...  

AbstractOsteocytes act as mechanosensors in bone; however, the underlying mechanism remains poorly understood. Here we report that deleting Kindlin-2 in osteocytes causes severe osteopenia and mechanical property defects in weight-bearing long bones, but not in non-weight-bearing calvariae. Kindlin-2 loss in osteocytes impairs skeletal responses to mechanical stimulation in long bones. Control and cKO mice display similar bone loss induced by unloading. However, unlike control mice, cKO mice fail to restore lost bone after reloading. Osteocyte Kindlin-2 deletion impairs focal adhesion (FA) formation, cytoskeleton organization and cell orientation in vitro and in bone. Fluid shear stress dose-dependently increases Kindlin-2 expression and decreases that of Sclerostin by downregulating Smad2/3 in osteocytes; this latter response is abolished by Kindlin-2 ablation. Kindlin-2-deficient osteocytes express abundant Sclerostin, contributing to bone loss in cKO mice. Collectively, we demonstrate an indispensable novel role of Kindlin-2 in maintaining skeletal responses to mechanical stimulation by inhibiting Sclerostin expression during osteocyte mechanotransduction.


2021 ◽  
Vol 9 (7_suppl3) ◽  
pp. 2325967121S0011
Author(s):  
Katie Kim ◽  
Michael Saper

Background: Gymnastics exposes the body to many different types of stressors ranging from repetitive motion, high impact loading, extreme weight bearing, and hyperextension. These stressors predispose the spine and upper and lower extremities to injury. In fact, among female sports, gymnastics has the highest rate of injury each year. Purpose: The purpose of this study was to systematically review the literature on location and types of orthopedic injuries in adolescent (≤20 years) gymnasts. Methods: The Pubmed, Medline, EMBASE, EBSCO (CINAHL) and Web of Science databases were systematically searched according to the Preferred Reporting Items for Systematic Reviews and Meta-analyses (PRISMA) guidelines to identify all studies reporting orthopedic injuries in adolescent and young adult gymnasts. All aspects of injuries were extracted and analyzed including location, type and rates of orthopedic injuries. Results: Screening yielded 22 eligible studies with a total of 427,225 patients. Twenty of 22 studies reported upper extremity injuries of which four specifically focused on wrist injuries. Eight studies reported lower extremity injuries. Nine studies reported back/spinal injuries. Seven studies investigated each body location of injury; one study reported the upper extremity as the most common location for injury and six studies reported the lower extremity as the most common location for injury. Of those seven studies, five (23%) reported sprains and strains as the most common injury. One study reported fractures as the most common injury. Conclusion: There is considerable variation in reported injury location. Some studies focused specifically on the spine/back or wrist. The type of gymnastics each patient participated in was also different, contributing to which area of the body was more heavily stressed, or lacking. Current literature lacks data to fully provide evidence regarding which body region is more frequently injured and the type of injury sustained.


Cells ◽  
2021 ◽  
Vol 10 (7) ◽  
pp. 1760
Author(s):  
Joshua J. A. Poole ◽  
Leila B. Mostaço-Guidolin

Biological tissues are not uniquely composed of cells. A substantial part of their volume is extracellular space, which is primarily filled by an intricate network of macromolecules constituting the extracellular matrix (ECM). The ECM serves as the scaffolding for tissues and organs throughout the body, playing an essential role in their structural and functional integrity. Understanding the intimate interaction between the cells and their structural microenvironment is central to our understanding of the factors driving the formation of normal versus remodelled tissue, including the processes involved in chronic fibrotic diseases. The visualization of the ECM is a key factor to track such changes successfully. This review is focused on presenting several optical imaging microscopy modalities used to characterize different ECM components. In this review, we describe and provide examples of applications of a vast gamut of microscopy techniques, such as widefield fluorescence, total internal reflection fluorescence, laser scanning confocal microscopy, multipoint/slit confocal microscopy, two-photon excited fluorescence (TPEF), second and third harmonic generation (SHG, THG), coherent anti-Stokes Raman scattering (CARS), fluorescence lifetime imaging microscopy (FLIM), structured illumination microscopy (SIM), stimulated emission depletion microscopy (STED), ground-state depletion microscopy (GSD), and photoactivated localization microscopy (PALM/fPALM), as well as their main advantages, limitations.


2006 ◽  
Vol 12 (4) ◽  
pp. 831-842 ◽  
Author(s):  
Sepideh Heydarkhan-Hagvall ◽  
Maricris Esguerra ◽  
Gisela Helenius ◽  
Rigmor Söderberg ◽  
Bengt R. Johansson ◽  
...  

Author(s):  
Shevryakov M.V.

This lecture is devoted to theoretical foundations of blood buffer systems functioning. Biochemical aspects and physiological activity of phosphate, hydrogen carbonate buffer and its combined activity with hemoglobin buffer, which ensures stability of blood pH, are presented. Chemical reactions to achieve the required blood pH are investigated. The combination of buffer properties, one of the components of which is CO2gas and autonomous self-regulation by intracellular hemoglobin ensures the blood plasma pH constancy. Stabilizing systems are considered -the respiratory apparatus and kidneys, which create the possibility of maintaining the stability of extracellular fluid pH. Respiratory acidosis, alkalosis, metabolic acidosis are considered on the biochemical level. This article presents information about hemoglobin structure: heme structure and globin subunits in different typesof hemoglobin. The following mechanismswhich provide maximumoxygen saturation of lungs and maximum oxygen emission in the tissues: heme-hemic interaction, Bohr effect and influence of 2,3-diphospho-glycerate connected with haemoglobin, are considered. The proteinbuffer system has been characterized in the in general. The capacity of the phosphate buffer system has been shown to be close to 1-2% of the whole buffer capacity of the blood and up to 50% of the buffer capacity of urine. The organic phosphates also exhibit buffering activity in the cell. Human and animal organisms can have intracellular pH from 4.5 to 8.5 depending on the type of cells, but the blood pH should be 7.4. This parameter is ensured by the hydrogen carbonate buffer system. Moreover,the blood pH depends not on the absolute concentrations of buffer components but on their ratio. The most powerful is hemoglobin buffer system that accounts for 75% of the whole blood buffer system. For stabilization of buffer capacity, the body uses two other stabilizing systems -the respiratory apparatus and kidneys. At the same time, the compensatory role of the respiratory system has shortcomings. Hyperventilation of lungs causes respiratory alkalosis. Hypoventilation has a counteracting effect by lowering the pH of the blood. Thus, the blood buffer system is ensured by a complex system that allows the organisms to adapt to changes in the fluid medium and regulate the pH under pathological conditions.Key words:homeostasis, hemoglobin, blood, acid-liquid equilibrium. У лекції розглядаються теоретичні основи механізмів дії буферних систем крові. Наводяться біохімічні аспекти та фізіологічна дія фосфатного, гідрогенкарбонатного буфера та його спільна дія з гемоглобіновим буфером, що забезпечує стабільність рН крові. Розглядаються хімічні реакції досягнення необхідного рівня рН крові. Поєднання властивостей буфера, одним з компонентів якого є газ СО2, та автономним саморегулюванням за рахунок внутрішньоклітинного гемоглобіну, забезпечує постійність рН плазми крові. Розглядаються стабілізуючі системи –дихальний апарат та нирки, які створюють можливості підтримання постійності рН позаклітинної рідини. На біохімічному рівні розглядаються дихальні ацидоз, алкалоз, метаболічний ацидоз. У статті представлені відомості про будову гемоглобіну: будову гему та субодиниць глобіну у різних видах гемоглобінів. Розглядаються механізми, що забезпечують максимальне насичення киснем легенів та максимальну віддачу кисню в тканинах: гем-гемова взаємодія, ефект Бора та вплив 2,3-дифосфо-гліцерату, зв’язаного з гемоглобіном. В загальних рисах охарактеризована білкова буферна система. Показано, що ємність фосфатної буферної системи становить близько 1-2% від всієї буферної ємності крові та до 50% буферної ємності сечі. При цьому органічні фосфати також виявляють буферну дію в клітині. В організмі людини і тварин значення внутрішньоклітинного рН може бути від 4,5 до 8,5 взалежності від типу клітин, проте рН крові має становити 7,4. Цей показник забезпечується гідрогенкарбонатною буферною системою. Причому, рН крові залежить не від абсолютних концентрацій компонентів буфера, а від їхнього співвідношення. Найбільш потужною є гемоглобінова буферна система, яка становить 75% від всієї буферної системи крові. Для стабілізації буферної ємності організм використовує ще дві стабілізуючі системи –дихальний апарат та нирки. Разом з тим, компенсаторна роль дихальної системи має недоліки. Гіпервентиляція легень спричиняє дихальний алкалоз. Гіповентиляція виявляє протилежну дію, знижуючи рН крові. Таким чином, буферна система крові забезпечується складною системою, що дозволяє організмові адаптуватися до змін оточуючого середовища та регулювати рН за патологічних умов.Ключові слова:гомеостаз, гемоглобін, кров, кислотно-лужна рівновага.


2001 ◽  
Vol 91 (1) ◽  
pp. 183-190 ◽  
Author(s):  
P. E. Mozdziak ◽  
P. M. Pulvermacher ◽  
E. Schultz

The hindlimb-unloading model was used to study the ability of muscle injured in a weightless environment to recover after reloading. Satellite cell mitotic activity and DNA unit size were determined in injured and intact soleus muscles from hindlimb-unloaded and age-matched weight-bearing rats at the conclusion of 28 days of hindlimb unloading, 2 wk after reloading, and 9 wk after reloading. The body weights of hindlimb-unloaded rats were significantly ( P < 0.05) less than those of weight-bearing rats at the conclusion of hindlimb unloading, but they were the same ( P > 0.05) as those of weight-bearing rats 2 and 9 wk after reloading. The soleus muscle weight, soleus muscle weight-to-body weight ratio, myofiber diameter, number of nuclei per millimeter, and DNA unit size were significantly ( P< 0.05) smaller for the injured soleus muscles from hindlimb-unloaded rats than for the soleus muscles from weight-bearing rats at each recovery time. Satellite cell mitotic activity was significantly ( P < 0.05) higher in the injured soleus muscles from hindlimb-unloaded rats than from weight-bearing rats 2 wk after reloading, but it was the same ( P > 0.05) as in the injured soleus muscles from weight-bearing rats 9 wk after reloading. The injured soleus muscles from hindlimb-unloaded rats failed to achieve weight-bearing muscle size 9 wk after reloading, because incomplete compensation for the decrease in myonuclear accretion and DNA unit size expansion occurred during the unloading period.


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