Little progress has been made to date towards the prevention of treatment of BPD. Even exogenous surfactant therapy, which acutely causes significant reductions in oxygen requirements and mortality from RDS, has had little impact on the 70-90% incidence of BPD in newborn survivors with birthweights of <1000 grams. The overall goal of this cooperative research program is to develop a multi-institutional research effort to address the mechanisms of postnatal lung pathobiology that lead to chronic lung disease and to provide a unique resource center of prematurely delivered baboons with induced bronchopulmonary dysplasia to outstanding investigators from multiple institutions dedicated to sharing collaborative protocols and tissue specimens. The baboon models of BPD are unique in the world; they develop disease that is very similar, if not identical, to the human disease but in a controlled environment. Unlike human clinical studies, gestational age is tightly controlled and results are not confounded by variable causes of premature delivery. The Southwest Biomedical Research Foundation has approximately 2700 baboons, the breeding colony and the scientific personnel to oversee all aspects of the proposed BPD Resource Core.
The specific aims of the BPD Resource Core are: 1) To breed baboons to produce pregnancies of known gestational ages, and to deliver by Caesarian section 100 timed pregnancies per year, to provide the premature infants that will be shared by multiple investigators. 2) To maintain these premature infant baboons in a neonatal intensive care environment for periods of up to 14 days, utilizing several well-defined treatment protocols. Long-term outcomes will be examined in 33-35 week survivors, the baboon equivalent of a 2 year old human infant in whom alveolarization should be complete. 3) To provide tissue specimens taken at the time of delivery, during the animal's clinical course, and at necropsy in as ideal and timely a manner as possible, and tailored to each investigator's needs. 4) To provide a Data Management Core for animal information retrieval.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Cooperative Clinical Research--Cooperative Agreements (U10)
Project #
5U10HL052636-05
Application #
2714062
Study Section
Special Emphasis Panel (ZHL1-CCT-G (M1))
Project Start
1994-07-20
Project End
1999-05-31
Budget Start
1998-06-01
Budget End
1999-05-31
Support Year
5
Fiscal Year
1998
Total Cost
Indirect Cost
Name
Southwest Foundation for Biomedical Research
Department
Type
DUNS #
City
San Antonio
State
TX
Country
United States
Zip Code
78245
Liao, Jie; Kapadia, Vishal S; Brown, L Steven et al. (2015) The NLRP3 inflammasome is critically involved in the development of bronchopulmonary dysplasia. Nat Commun 6:8977
Blanco, Cynthia L; McGill-Vargas, Lisa L; Gastaldelli, Amalia et al. (2015) Peripheral insulin resistance and impaired insulin signaling contribute to abnormal glucose metabolism in preterm baboons. Endocrinology 156:813-23
Blanco, Cynthia L; Moreira, Alvaro G; McGill-Vargas, Lisa L et al. (2014) Antenatal corticosteroids alter insulin signaling pathways in fetal baboon skeletal muscle. J Endocrinol 221:253-60
Yoder, Bradley A; Coalson, Jacqueline J (2014) Animal models of bronchopulmonary dysplasia. The preterm baboon models. Am J Physiol Lung Cell Mol Physiol 307:L970-7
Blanco, Cynthia L; McGill-Vargas, Lisa L; McCurnin, Donald et al. (2013) Hyperglycemia increases the risk of death in extremely preterm baboons. Pediatr Res 73:337-43
Quinn, Amy R; Blanco, Cynthia L; Perego, Carla et al. (2012) The ontogeny of the endocrine pancreas in the fetal/newborn baboon. J Endocrinol 214:289-99
Shields, Amy; Thomson, Merran; Winter, Vicki et al. (2012) Repeated courses of antenatal corticosteroids have adverse effects on aspects of brain development in naturally delivered baboon infants. Pediatr Res 71:661-7
Waleh, Nahid; McCurnin, Donald C; Yoder, Bradley A et al. (2011) Patent ductus arteriosus ligation alters pulmonary gene expression in preterm baboons. Pediatr Res 69:212-6
Waleh, Nahid; Seidner, Steven; McCurnin, Donald et al. (2011) Anatomic closure of the premature patent ductus arteriosus: The role of CD14+/CD163+ mononuclear cells and VEGF in neointimal mound formation. Pediatr Res 70:332-8
Rees, Sandra; Loeliger, Michelle; Shields, Amy et al. (2011) The effects of postnatal estrogen therapy on brain development in preterm baboons. Am J Obstet Gynecol 204:177.e8-14

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