ULTRAVIOLET LIGHT INDUCED CONNECTIVE TISSUE CHANGES IN RAT SKIN: A HISTOPATHOLOGIC AND HISTOCHEMICAL STUDY*

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THE JOURNAL OF INVESTIGATIVE DERMATOLOGY Copyright 1968 by The Williams & Wilkins Co. Vol. 51, No. 4 Printed in U.S.A. ULTRAVIOLET LIGHT INDUCED CONNECTIVE TISSUE CHANGES IN RAT SKIN: A HISTOPATHOLOGIC AND HISTOCHEMICAL STUDY* KJNUYO NAKAMURA, MD.t AND WAINE C. JOHNSON, M.D. It is gerierally accepted that chroriic exposure to sunlight results in solar elastosis of human skiri. However, experimental production of cutaneous elastotic changes in animals using artificial ultraviolet light has only rarely been reported. Utilizing histochemical methods, Sams, Smith arid Burk demoristrated focal dermal elastosis iii mice following proloriged exposure to artificial ultraviolet light (1). The purpose of this paper is to record our observations ori ultraviolet light iriduced coririective tissue chariges iii rat skiri. MATERIALS AND METHODS The animals used for this investigation were Fischer strain 344 albino female rats weighing approximately 100 grams at the onset of the experiment. Thirty animals were shaved on the dorsum with electric clippers weekly and exposed to ultraviolet light (UVL) three days a week for a total period of 27 weeks. Fifteen animals were used as controls and were shaved weekly but were not exposed to IJVL. The exposure to UVL was for 20 minutes at a distance of 62 centimeters from a bank of 4 Westinghouse FS 40 fluorescent sun lamps. Biopsies from the dorsum of 4 treated animals and 2 control animals were taken after one week of TJVL exposure and subsequently at 2 week intervals throughout the 27 week period of light exposure and afterward for a total period of 46 weeks. At 46 weeks, all of the IJVL treated animals and all control animals were sacrificed for additional histopathologic and histochemical studies. Onehalf of each tissue specimen was frozen on solid carbon dioxide and the remainder was embedded in paraffin. Fifty microns cryostat sections were processed for demonstration of blood vessels using the alkaline phosphatase technique * From The Departments of Dermatology and Pathology, Temple University School of Medicine; and The Skin and Cancer Hospital of Philadelphia, Philadelphia, Pennsylvania 19140. t Present address: Department of Dermatology, Keio University, Tokyo, Japan. Presented at the Special Meeting of the Society for Investigative Dermatology, Inc., May 4, 1968, Atlantic City, N. J. This study was supported by Research Grants ES 00269 and CA 05189 from the USPHS. Reprint requests to The Skin and Cancer Hospital of Philadelphia, 3322 North Broad Street, Philadelphia, Pennsylvania, 19140 (Dr. Johnson). (2), and 12 microns cryostat sections were used for demonstration of elastic tissue with the aldehydefuchsin stain at ph 1.7 (3). The following procedures were performed on paraffin embedded tissue sections from each specimen: hematoxylin and eosin; periodic acidschiff (PAS) reaction with and without diastase digestion; colloidal iron reaction with and without bovine testicular hyaluronidase digestion for one hour at 37 C (3); alcian blue stain at ph 2.5 and 0.4 (3); aldehydefuchsin stain at ph 1.7 at 0.4 (3); Movat's pentachrome I stain (4); and Snook's reticulum stain (5). RESULTS Macroscopic Changes. The ariimals exposed to UVL showed a mild diffuse erythema ori the dorsum after orie week. After two weeks the ears showed mild erythema and telarigiectasia, and this charige contiriued duririg the period of exposure. Most of the ariimals showed severe erythema, scaling, arid crustirig of the dorsum by five weeks arid gross chariges progressed to include ulcerations arid alopecia of varying degrees from 9 weeks uritil UVL was discoritiriued at 27 weeks. The skiri began to heal after UVL was stopped but some scarririg arid mild erythema remairied. Two ariimals developed a papilloma on UVL exposed sites on the back of the ears. No abnormal chariges were seen in the coritrol animals. Histopathologic and Histochemical Observations. The superficial corium showed mild to moderate interstitial edema arid a miriimal perivascular cellular irifiltratiori after three weeks of UVL exposure. Ari increased riumber of lymphocytes and histiocytes were seen at 5 weeks, and after 7 weeks was more promirierit and the cellular infiltrate included polymorphonuclear leukocytes, fibrocytes arid mast cells. Cellular irifiltratiori arid edema iri the superficial corium coritiriued to iricrease until the 19th week after which it remairied relatively constarit up to 27 weeks wheri exposure to UVL was stopped. After 27 weeks, fibrocytic proliferatiori became proriouriced. Edema arid iriflammatiori rapidly subsided. Histologic examinatiori of the two tumors on the ears disclosed 253

254 THE JOURNAL OF INVESTIGATIVE DERMATOLOGY.1,, Fm. 1. Prominent increase in ground substance acid mucosaccharide is present alter 7 weeks of TJVL. Colloidal iron, X 120. / / a 4 I 'I simple papillornas. No abnormal changes were seen in the control animals. Hernatoxylin and eosin, and PASstained sections were used to study collagen fibers. Snook's method was used for evaluation of reticular fibers. An increased number of reticular fibers appeared in the superficial corium after TJVL was discontinued. Mild fibrosis of collagen fibers was observed in the superficial corium in most sections taken at 46 weeks. Acid mucosaceharides of the extraceliular interfibrillar ground substance began showing a prominent increase in the superficial corium after 3 weeks of exposure to UVL. The amount of acid mucosaccharide increased for several weeks and then remained relatively constant during the remainder of the exposure period (Figs. 1 and 2). The quantity of the ground substance acid rnucosaccharide gradually decreased toward normal after UVL was stopped. The histochemical properties of the acid mucosaccharide were as follows: colloidal iron positive and partially hyaluronidase labile, alcian blue positive at ph 2.5 and negative at 0.4, and aldehydefuchsin negative. Initially, most of the ground substance acid mucosaccharide was removed by hyaluronidase digestion; but after several weeks a larger proportion of this material was hyaluronidase resistant. The above reactions indicate the presence of hyaluronic acid and possible other unidentifiable mucosaccharides. Dilatation and increased tortuosity of the blood vessels in the superficial coriurn were observed in alkaline phosphatase preparations of animals exposed to TJVL after 7 weeks. After 15 to 17 weeks of UVL exposure, alkaline phosphatase positive fibrocytic cells were seen about the papillary capillaries, and subsequently, diffuse alkaline phosphatase activity appeared in the stroma about the capillaries. The blood vessels of control animals were normal and fibrocytes were alkaline phosphatase negative. Elastic tissue was evaluated with aldehydefuchsin stained cryostat sections, and with aldehydefuchsin and the Movat stained paraffin tissue sections. The aldehydefuchsin stained cryostat sections gave the best demonstration of elastic tissue after UVL exposures. Elastic tissue in the superficial corium gradually diminished as the inflammatory cellular infiltrate

1 U : Fig. 2. Normal skin of control animal at 7 weeks for comparison with Fig. 1. Colloidal iron, X 120. t : C a. _. 2 A 7_ cc A iz1 :.. /ii b r Fig. 3 A few fine new elastic fibers are present in the supeficial corium at 33 weeks in the area where the elastica was previously destroyed by inflammation: Elastic fibers adjacent to the hair follicles seen in the middle corium generally remained intact and were not destroyed by the infiltrate. Aldehydefuchsin ph 1.7, X 92. 255

256 THE JOURNAL OF INVESTIGATIVE DERMATOLOGY 1W Fxc. 4. Numerous fine to thick elastic fibers are present in the superficial corium at 46 weeks. Aldehydefuchsin ph 1.7,)< 92. FIG. 5. Higher power of magnification of Fig. 4 shows variable sized elastic fibers and some interfibrillar reactive amorphous material. Aldehydefuchsin ph 1.7, )< 165.

UVL AND TISSUE CHANGES 257 ¼. FIG. 6. Normal skin of control rat at 46 weeks for comparison with the elastic fiber changes demonstrated in Figs. 3, 4 and 5. Alclehyclefuchsin ph 1.7, X 92. increased. Most of the elastic fibers in the superficial corium were destroyed by 23 weeks and remained virtually absent until the TJVL was discontinued. Specimens obtained at 33 weeks (Fig. 3) showed formation of new elastic tissue in the superficial corium as fine fibers and these increased in number and thickness throughout the remainder of the period of observatiori to 46 weeks. Dense collections of elastic fibers were located in the superficial corium and about the hair follicles and these changes were separated from the epidermis by a narrow grenz zone. The amount of elastic tissue in the superficial corium at 46 weeks (Figs. 4 and 5) was significantly greater than that seen in the control untreated animals (Fig. 6). Some tissue sections obtained at 46 weeks from animals exposed to IJYL showed granular or amorphous interfibrillar material which was reactive with elastic stains and was localized to the areas of elastotic change. The grenz zone, the elastotic changes, and ground substance alterations closely resembled solar elastosis of human skin. COMMENT Dilatation and tortuosity of capillaries in the superficial corium appeared relatively early after exposure to UVL and these vascular changes probably represent a direct response to irradiation. We have observed similar changes in papillary capillaries seen in solar elastosis and precancerous dermatoses of human skin. An increase in ground substaiice acid mucosaccharide with histochemical properties of hyaluronic acid was a striking early change. Mathieson and Pearce (7) performed chemical analysis of the acid mucosaccharide of the ground substance of normal rat skin. They found hyaluronic acid to be present but were unable to detect chondroitin sulfates. The amount of acid mucosaceharide decreased prior to and during the period of increased elastic tissue formation. Sams, Smith and Burk (1) also observed an increased amount of acid mucosaccharide in the superficial corium in mice treated with ultraviolet light. Previous studies (6) indicate dermal fibrocytes represent one source of hyaluronic acid arid that an increased

258 THE JOURNAL OF INVESTIGATIVE DERMATOLOGY production of this acid mucosaccharide is usually associated with a decreased production of collagen and elastica. Not all of the colloidal iron positive material which accumulated in the superficial corium in rats exposed to UVL was removed by hyaluronidases digesticin; this is similar to our experience that not all of the colloidal iron positive material associated with solar elastosis of humans is removed by short periods of digestion with hyaluronidase (8). The delay of elastic tissue proliferation was probably due to inflammation present during the period of UVL exposure since the cellular infiltrate destroyed much of the normal elastic fibers present and apparently retarded new fiber formation. The results obtained in our study stress the necessity of stopping exposure to IJYL before a significant increase in elastic tissue production occurs in rat skin, and probably explain why most attempts at experimental production of dermal elastosis in animals have been unsuccessful. The grenz zone observed in our study was also reported by Sams, Smith and Burk (1) and this change is commonly seen in human solar elastosis. Our histopathologic and histochemical studies show evidejice of increased elastic tissue production in the superficial corium in rats exposed to IJYL and these changes are similar to solar elastosis in man after chronic actinic irradiation. The question as to whether other types of injury may also produce elastosis is unsettled. An increase in elastic fibers has been reported as occurring following application of carcinogens to mouse skin (9). Sams, Smith and Burk (1) did not find evidence of elastosis in mice treated with a primary irritant. Our results indicate a need for additional evaluation of experimental production of elastosis. We plan to further evaluate this problem by use of primary irritant and carcinogens as controls; chemical analysis of tissue showing histochemical evidence of elastosis; and varying the amount and intervals of exposure to ultraviolet light. SUMMARY The effect of UVL on connective tissue of rat skin was studied using histopathologic and histochernical methods. Thirty female albino rats were exposed to IJYL 3 days a week for 27 weeks. Biopsies were taken from UVL exposed and control animals every two weeks during a 46 week period. A prominent increase in acid niucosaccharide with histochemical properties of hyaluronic acid occurred in the superficial corium after three weeks of UVL exposure and diminished when the UVL was stopped. Alkaline phosphatase studies demonstrated significant vascular changes, reactive dermal fibrocytes, and focal diffuse alkaline phosphatase activity in the stroma of the papillary corium. As edema and cellular infiltration in the superficial corium increased elastic fibers disappeared and remained virtually absent while exposure to light was continued. New elastic tissue fibers appeared in the superficial corium after IJYL was stopped and elastica gradually increased to abnormal quantities closely simulating solar elastosis of human skin. REFERENCES 1. Sams, W. M., Jr., Smith, J. G. and Burk, P. G.: The experimental production of elastosis with ultraviolet light. J. Invest. Derm., 43: 467, 1964. 2. Menne, H. L. and Johnson, W. C.: A resinous mounting medium compatible with azodye staining for alkaline phosphatase. Stain Technol., 41: 295, 1966. 3. Johnson, W. C.: Histocheinistry of the cutaneous ground substance, pp. 35 Si, Methods and Achievements in Experimental Pathology, Vol. 1. Eds., Bajusz, E. and Jasmin, G. G., Karger, Basel and New York, 1966. 4. Movat, H. Z.: Demonstration of all connective tissue elements in a single section. Arch. Path. (Chicago), 60: 289, 1955. 5. Armed Forces Institute of Pathology. Manual of Histologic and Special Statnimg Technics, 2nd Ed. The Blakiston Division, McGrawHill Book Company, Inc., New York, 1960. 6. Johnson, W. C. and Helwig, E. B.: Cutaneous focal mucinosis. Arch. Derm., 93: 13, 1966. 7. Mathieson, J. M. and Pearce, R. H.: The glycosaminoglycan of the ground substance of rat skin. Canad. J. Biochem., 41: 2327, 1963. 8. Johnson, W. C. and Helwig, E. B.: Histochemistry of the acid mucopolysaccharides of skin in normal and certain pathologic conditions. Amer. J. Clin. Path., 40: 123, 1963. 9. Ma, C. K.: Morphological and chemical investigation of dermal elastic, and collagenic tissue during epidermal carcinogenesis. Cancer Res., 9: 481, 1949.