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THE EFFECTS OF AGE AND PHYSIOLOGICAL FACTORS ON THE PERMEABILITY AND HISTOLOGY OF SYNOVIAL TISSUE IN THE RAT PDF

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INFORMATION TO USERS This material was produced from a microfilm copy of the original document. While the most advanced technological means to photograph and reproduce this document have been used, the quality is heavily dependent upon the quality of the original submitted. The following explanation of techniques is provided to help you understand markings or patterns which may appear on this reproduction. 1. The sign or "target" for pages apparently lacking from the document photographed is "Missing Page(s)". If it was possible to obtain the missing page(s) or section, they are spliced into the film along with adjacent pages. This may have necessitated cutting thru an image and duplicating adjacent pages to insure you complete continuity. 2. When an image on the film is obliterated with a large round black mark, it is an indication that the photographer suspected that the copy may have moved during exposure and thus cause a blurred image. 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Xerox University Microfilms 300 North Zeeb Road Ann Arbor, Michigan 48106 13- 2.2/Z85 s LDj907 I .C-7 Moffett, Benjardn Charles, 19'23- 1952 The effects of age and physiological i ,i,:6 factors on the permeability and histo­ logy of synovial tissue in the rat. Mi?P» illu s . tables. Thesis (Ph.D.) - il.Y.U., Graduate vchcol, 1952. Bibliography: p .!;l4j.5. C98321 Shelf List Xerox University Microfilms, Ann Arbor, Michigan 48106 THIS DISSERTATION HAS BEEN MICROFILMED EXACTLY AS RECEIVED. LIBRARY tf new tori miiTiRsrn UNIVERSITY HEIfiHTR The Effects of Age and Physiological Factors 1 on the Permeability and Histology of Synovial Tissue in the Rat Benjamin C."Moffett Jr. A dissertation in the department of Anatomy submitted in partial fulfillm ent of the requirements for the Degree Doctor of Philosophy, at New York University. June 1952 Table of Contents page Introduction 1 Embryology of Synovial Tissue - - - - - - ----------- 1 Anatomy of Synovial Tissue - - - - - - - - - - - -- 3 Histology - - - - - - - - - - - - - - - - - - 3 Synovial Cells - - - - - - - - - - - - - - - 3 Innervation - - - - - - - - - - - - - - - - - 4- Blood Supply and Lymphatics - - - - - - - - - 5 Synovial Fluid - - - - - - - - - - - - - - - 6 Permeability of Synovial Tissue - - - - - - - - - 3 General Description - - - - - - - - - - - - - 8 Manner of Fluid Exchange - - - - - - - - - - 8 Effect of Pressure - - - - - - - - - - - - - 8 Effect of Exercise - - - - - - - - - - - - - 9 Effect of Joint Position - - - - - - - - - - 1 0 Other Factors - - - - - - - - - - - - - - - -1 0 Permeability Changes Associated with Joint Pathology - - 11 Problem - - - - - - - - - - - - - - - - - - - - - 1 2 Development of Method - - - - - - - - - - - 1 3 Effects of Age - - - - - - - - - - - - - - - 14, Endocrine Influences - - - - - - - - - - - - 14. Histology and Histochemistry - - — - - - - - 14, page II. Procedure and Methods - - - - - - - - - . - - - - - - - 1 4 Synovial Permeability* Development of Method - - 14 Experimental Groups - - - - - . - - - - - - - - - - 1 6 Histology and Histochemistry - - - - - - - - - - - 1 8 III. Observations - - - - - - - - - - - - - - - - - - - - - 1 9 Synovial Permeability - - - - - - - - - - - - - - 19 Ground Substance - - - - - - - - - - - - - - - - - 2 0 Blood Supply - - - - - - - - - - - - - - - - - - - 2 1 Effects of Age - - - - - - - - - - - - - - - - - -2 2 Endocrine Influences - - - - - - - - - - - - - - - 2 4 Histology and Histochemistry - - - - - - - - - - - 2 6 IV, Discussion - - - - - - - - - - - - - - - - - - - - - -2 9 Synovial Permeability: Methods for Testing - - - 29 Ground Substance* Histochemical Methods - - - - - 31 Effects of Age - - - - - - - - - - - - - - - - - - 3 2 Endocrine Influences - - - - - - - - - - - - - - - 3 4 V, Summary and Conclusions - - - - - - - - - - - - - - - 3 7 VI. Foot Notes - - - - - - - - - - - - - - - - - - - - - - 3 9 VII. Bibliography - - - - - - - - - - - - - - - - - - - - - 41 The Effects of Age and Physiological Factors On the Permeability and Histology of Synovial Tissue in the Rat I. Introduction The recent progress in the treatment of joint pathology following the discovery by Hench et al (1) that cortisone affects the course of rheumatoid arthritis has been an incentive for this study of joint permeability. Basically this thesis is concerned with the development of a technique suitable for measuring the permeability of synovial tissue and then using this technique to determine what factors affect that permeability. An histological study is included to show what structural changes are associated with an altered per­ meability. Before considering the results of this work, a review of the literature on the embryology, anatomy, and physiology of synovial joints is essential. Embryology of Synovial Tissue The development of synovial joints is well described by Haines (2). In the 11 mm human fetus chondrification centers appear in the mesenwhymatous skeletal blastema. These centers grow by apposition and form cartilage models of the developing bones. The unchondrified blastema between these cartilages becomes reduced In thickness to form a narrow interzone or primitive joint plate which is the first indica­ tion of a joint. 2 - - At 16 mm the interzones of the larger joints are contin­ uous with the perichondrium surrounding the cartilages. The future joint capsules are seen as curving strata of cells arranged longitu­ dinally, passing around the joint regions. Between this capsule and the perichondrium around the ends of the cartilage is the undifferen­ tiated synovial mesenchyme. Small blood vessels pierce the capsule and enter the synovial mesenchyme. At 21 mm the interzones or areas between the embryonic cartilages of some joints differentiate into a chondrogenous portion which w ill form the articular surfaces and a central or intermediate loose layer which is continuous peripherally with the synovial mesen­ chyme. The chondrogenous layers are continuous peripherally with the perichondrium and together they completely invest the end of the skel­ etal element. At 29 mm the synovial tissue at the periphery of the joint breaks down. At 30 mm the interzones and inner synovial mesenchyme begin to break down. The ground substance becomes liquefied leaving a cellular network. Most of these cells migrate to form a lining on the walls of the cavity. These cavities appear in the larger joints at or soon after the onset of periosteal ossification in the long bones. The remains of the liquefied interzone or synovial mesenchyme form a thin fib rillar layer of flattened cells over the cartilage but these dfeappear later. At first the synovial surfaces are ragged but as the extension of the cavity slows down the surface of the capsule becomes smoothed off and covered with a layer of synovial cells. The joint capsule becomes continuous with the perichondrium over the chondrified blastema and differentiates into dense fibrous tissue. 3 - - Anatomy of Synovial Tissue The synovial tissue lines the joint everywhere except over the articular cartilages. Projections of it extend into the joint cavity. The small ones, called synovial v illi, are merely fibrous tufts with cells embedded in them and scattered about their surfaces. Synovial folds are larger projections involving a folding of the whole thickness of the tissue. These may present secondary folds which when clustered together and covered with v illi are called synovial fringes. They increaeeythe surface area of the synovial tissues and also the rapidity with which substances diffuse into and out of the joint cavity. Microscopically the synovial tissue is composed of a colla­ genous groundwork containing connective tissue cells. The thickness and cell content vary in different parts of the joint. The synovial cells are not greatly differentiated and therefore are capable of rapid repair. Key (3) demonstrated this by removing synovial tissue from the knees of rabbits. This was quickly followed by fibrin formation and in fil­ tration of connective tissue cells from the capsule. Within sixty days, the newly formed tissue could not be distinguished from the undamaged tissue around it. Le Gros Clark (4) showed that synovial cells are not primarily phagocytic in function by injecting trypan blue into a rabbit's knee joint. It required twelve hours before the synovial cells took up the dye as granules and even then the granules were fine and discrete as compared to the coarse clumped ones usually seen in clasmatocytes. The synovial tissue may lie directly on the fibrous capsule 4 - - of the joint or be separated from it by other connective tissue. On this basis Key (5) classifies synovial tissue into three types: fibrous, are­ olar, and adipose. The fibrous type is found over areas subjected to a continuous pressure, such as ligaments, tendons, or fibrocatilage. Here the synovial tissue is thinned out; its cells are widely separated from each other and are difficult to distinguish from fibroblasts. Most of the lining is composed of intercellular substance. The areolar type of synovial tissue is found where mobility is required. Here the synovial tissue is thickest, often consisting of three or four layers of cells embedded in collagenous fibers which blend with those of the areolar tissue. Davies (6) describes elastic fibers in the areolar synovial tissue which prevent it from being caught between the articular surfaces during movement of the joint. The adipose type of synovial tissue covers the intraarticular fat pads which bulge into the cavity fillin g up the irregularities in the intraarticular surfaces. The surface cells usually form a single layer which appears to rest on the adipose tissue but these cells are also em­ bedded in collagenous fibers. Thus there are three histological types of synovial tissue, a ll of which may be found in a single joint. The review by Gardner (7) indicates that there is no agreement on the types of nerve endings to be found in synovial tissue. The synovial blood vessels are innervated by myelinated and non-rayelinated fibers but it is not certain whether the function of synovial tissue can be altered by these nerves. Engel (3) says that sympathectomy alters the passage of dyes into the joint space but Cheng (9) could not confirm this. A different vascular pattern has been described by Davies (10) for each type of synovial tissue. In areolar areas the larger arteries ’ and veins run deeply forming a wide-meshed plexus parallel to the synovial surface. This plexus sends branches into the synovial tissue forming a smaller meshed plexus closer to the surface which in turn supplies a third irregularly quadrilateral plexus of arterioles and venules very close to the surface. The third plexus gives off many terminal capillaries with the result that this superficial portion is richly vascularized. There are usually two veins following each artery. Halves are frequent in all veins. In adipose synovial tissue, the larger vessels enter directly into the base of the fat pad and branch in tree-fashion. There is no specialized capillary net at the joint surface. In fibrous areas, arterioles and venules run longitudinally between the connective tissue fibers. Small transverse vessels connect them. In general the characteristics of the synovial blood supply are multiple origins of supply, voluminous terminal veins with many valves, frequent anastomoses, and a superficial capillary plexus. The vascular pattern in the areolar areas allows the fastest rate of fluid exchange to take place here. Davies (10) has found that lymphatics are few in number and lie deep in synovial tissue. They begin as blind tubes which converge into large vessels passing toward the flexor aspect of the joint. They anastomose with the periosteal lymphatics and then empty into the main lymphatic vessels of the limb.

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