1978
DOI: 10.1016/0012-1606(78)90287-7
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Alkaline phosphatase and maltase activity in the embryonic chick intestine in culture

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1978
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Cited by 70 publications
(35 citation statements)
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“…cortisone and thyroxine. Indeed the observations of Black and Moog [1] indicating that insulin not only has no effect on maltase and alkaline phosphatase activities of chick embryo small intestine in organ culture but also inhibits the increases of activities induced by cortisone and thyroxine, suggested that this phenome non could be generalized to mammalian small intestine. The present investigation us ing suckling mice confirms that insulin accel erates the development of the brush border membrane hydrolytic activities [20] and shows that there is no antagonism between insulin and cortisone or thyroxine on maltase and alkaline phosphatase activities.…”
Section: Discussionmentioning
confidence: 99%
“…cortisone and thyroxine. Indeed the observations of Black and Moog [1] indicating that insulin not only has no effect on maltase and alkaline phosphatase activities of chick embryo small intestine in organ culture but also inhibits the increases of activities induced by cortisone and thyroxine, suggested that this phenome non could be generalized to mammalian small intestine. The present investigation us ing suckling mice confirms that insulin accel erates the development of the brush border membrane hydrolytic activities [20] and shows that there is no antagonism between insulin and cortisone or thyroxine on maltase and alkaline phosphatase activities.…”
Section: Discussionmentioning
confidence: 99%
“…The cells of the connective tissue through their interaction with the epithelium via connective tissue matrix are in a position to mediate influences on epithelial cells. Thus, corticosteroids, for example, may affect epithelial cell differentiation, both directly (28) or indirectly (29). Cytokines, also, may have different effects on the epithelium in contact with fibroblasts than in enterocytes alone (30).…”
Section: Discussionmentioning
confidence: 99%
“…Furthermore, insulin exerted a sustained effect on crypt cell proliferation [17], It is, however, difficult to conclude whether or not these modifications resulted from a direct action of insulin on the intestinal mucosa or represented a response to a systemic reaction such as for example the transient hypoglycemia caused by insulin [ 19], Because organ culture removes the stud ied tissue from the interacting complexities of the intact organism, it permits a more sys tematic approach to the study of the intrinsic and extrinsic regulators of intestinal epithe lial maturation than is possible in vivo [11,30]. This methodology made it possible to investigate the ontogenetic development of the intestine of the fetal rat, mouse and chick [3,5,6], Few investigations have been de voted to the analysis of intestinal develop-mcnt in vitro using suckling intestine [ 12,28,29]. Since we recently reported the successful maintenance of suckling mouse small intes tine in a serum-free medium [ 16], the present investigation was undertaken to determine the possible direct effect of insulin on the development of the hydrolytic functions of the brush border and on the proliferation of the crypt cells of suckling mouse small intes tine maintained in organ culture.…”
Section: Introductionmentioning
confidence: 99%