Oxygen-Induced Retinopathy in the Newborn Rat: Morphological and Immunohistological Findings in Animals Treated with Topical Timolol Maleate

2000 ◽  
Vol 214 (2) ◽  
pp. 136-139 ◽  
Author(s):  
Benedetto Ricci ◽  
Francesco Ricci ◽  
Nicola Maggiano
1991 ◽  
Vol 77 (1) ◽  
pp. 47-56 ◽  
Author(s):  
Benedetto Ricci ◽  
Giuseppe Calogero ◽  
Alessandra Caprilli ◽  
Francesco M. Quaranta-Leoni

PEDIATRICS ◽  
1988 ◽  
Vol 82 (2) ◽  
pp. 193-198
Author(s):  
Benedetto Ricci ◽  
Giuseppe Calogero

An experimental study was conducted to verify the effects of prolonged normobaric and hyperbaric oxygen supplementation on retinal vessels in newborn animals. Nine litters of newborn Wistar rats were used in the following way. Two litters were used as controls. Two other litters received normobaric oxygen supplementation (FiO2 80%) for five days after birth. These rats were then removed and kept for five more days in room air. Retinopathy with marked peripheral retinal neovascularization was seen in these litters. Three other litters were exposed to the same treatment for ten days after birth, removed from oxygen, and kept for 15 more days in room air. Severe retinopathy with extraretinal proliferation and, in some cases, retinal detachment developed in these animals. Two other litters received hyperbaric (1.80 atm) oxygen supplementation (FiO2 80%) for ten days after birth and were then kept for 15 days in normobaric room air. These animals showed no evidence of peripheral retinopathy. It is possible that moderate hyperbarism exerts, in the newborn rat, a protective action against the toxic effects of oxygen supplementation on immature retinal vessels.


1991 ◽  
Vol 76 (3) ◽  
pp. 241-249 ◽  
Author(s):  
Benedetto Ricci ◽  
Domenico Lepore ◽  
Enrico Zonghi ◽  
Giuseppe Calogero

1980 ◽  
Vol 93 (3) ◽  
pp. 339-345 ◽  
Author(s):  
Naokazu Nagata ◽  
Yuriko Ono ◽  
Narimichi Kimura

Abstract. The interaction between parathyroid hormone (PTH) and prostaglandin E1 (PGE1) in influencing cyclic AMP metabolism in rat renal cortical tissue was examined. PTH and PGE1 stimulated additively the adenylate cyclase activity in the homogenate of the tissue. Both PTH and PGE1 enhanced the level of cyclic AMP in the incubated renal cortical tissue, but the effect of their simultaneous addition did not exceed the effect induced by PTH alone. Cyclic AMP accumulated in the incubation medium by stimulation by PTH was decreased by the simultaneous addition of PGE1. When the tissue was pre-incubated for 30 min with 2 to 10 μg/ml of PGE1, the magnitude of the increase of cyclic AMP caused by PTH subsequently added was lessened. However, the response to PTH of adenylate cyclase preparation obtained from the homogenate of PGE1-pre-treated tissue was not decreased. When first PTH was added to the incubating renal cortical tissue, the subsequent addition of PGE1 accelerated the decrease of cyclic AMP content in the tissue and decreased the amount of cyclic AMP released from the tissue. The interaction of PTH and PGE1 on cyclic AMP metabolism in the renal cortical tissue was in contrast to that seen in newborn rat calvaria where PGE1 and PTH acted additively in enhancing the level of cyclic AMP.


2021 ◽  
pp. 108716
Author(s):  
Yuying Sun ◽  
Yao Ni ◽  
Ning Kong ◽  
Chunyu Huang

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