Ll litter, SL) on P3, while normal litters (NL) were culled to 10 pups per litter and nurtured by their own mother as control. The male pups were weaned onto standard chow diet on P21 and housed 3 per cage. Food and water were available ad libitum unless fasting 
was required for the experiment. These mice were sacrificed by decapitation on P21 and P150 between 10:00 and 12:00 AM. Each group contained 10?5 mice.Glucose Tolerance Test (GTT)GTT was performed on P120. After 16 hours of fasting, the mice from NL and SL received a 20 glucose solution (2 g/kg) through intraperitoneal injection. Blood glucose concentration was measured from the tail vein immediately at 0, 15, 30, 60 and 120 minutes after glucose loading. Blood glucose levels were measured using a glucometer (SureStep OneTouch, Amecira) [29]. Area under the curve (AUC) measurement across 120 min was determined from the average for each animal, using the trapezoidal method with baseline set as the blood glucose levels at 0 min.Determination of Airway HyperresponsivenessAirway hyperresponsiveness was examined on P21 and P150. The tested mice were put into the whole-body plethysmograph (EMKA Technologies, Paris, France). Mice were exposed to aerosolized saline (for the baseline measurement) and increasing concentrations of methacholine (3.125, 6.25, 12.5, 25, 50 mg/ml) for 3 min each. Data were recorded and averaged for 5 min after 2 min rest. The index of airflow obstruction was expressed as enhanced pause (Penh, dimensionless parameter), which correlates with pulmonary airflow resistance. Penh is a dimensionless value that represents a function of the ratio of peak expiratory flow (PEF) to peak inspiratory flow (PIF) and a function of the timing of expiration (Pause) (Penh = PEP/PIF6Pause). Penh was calculated based on the EMKA Datanalyst provided by EMKA Technologies.BALF AssaysMice were anesthetized with 10 chloral hydrate, exsanguinated and then sacrificed. The trachea was cannulated and bronchoalveolar lavage fluid (BALF) was collected by three injections of 0.5 ml phosphate-buffered saline (PBS) into lungs. Total BALF cells were collected by centrifugation, treated with red blood lysis buffer to remove the red blood cells and counted by microscopy using cell counter. Classified cells were performed with Wright iemsa, and then counted on a total of 200 cells under immersion oil at61,000 magnification. The remaining lavage fluid was centrifuged at 1500 r/min for 10 min and the collected supernatant was analyzed for cytokine TNF-a.Materials and Methods Ethics StatementAll animal studies were performed in accordance with the Guide for the Care and Use of Laboratory Animals of the National Institutes of Health. All animals care and experimental protocols were approved by the Ethical Principles in Animal Research adopted by the Chongqing Medical University for Animal Experimentation.Neonatal Overfeeding and Airway ResponsivenessHistological AnalysisThe left 12926553 lungs were fixed in 4 paraformaldehyde at least for 72 h,dehydrated in graded alcohol series, Castanospermine cleared with dimethylbenzene, and embedded in paraffin. Serial sections of 5 mm thickness were stained with hematoxylin-eosin (H E). Lung fibrosis was evaluated by Masson 3PO site staining for collagen accumulation according to the manufacture’s protocols. Bronchi and lung alveoli were evaluated under a Nikon Eclipse E200 microscope adapted to a Nikon Coolpix 995 camera. Total inflammatory cell counts were determined from these images at 400.Ll litter, SL) on P3, while normal litters (NL) were culled to 10 pups per litter and nurtured by their own mother as control. The male pups were weaned onto standard chow diet on P21 and housed 3 per cage. Food and water were available ad libitum unless fasting was required for the experiment. These mice were sacrificed by decapitation on P21 and P150 between 10:00 and 12:00 AM. Each group contained 10?5 mice.Glucose Tolerance Test (GTT)GTT was performed on P120. After 16 hours of fasting, the mice from NL and SL received a 20 glucose solution (2 g/kg) through intraperitoneal injection. Blood glucose concentration was measured from the tail vein immediately at 0, 15, 30, 60 and 120 minutes after glucose loading. Blood glucose levels were measured using a glucometer (SureStep OneTouch, Amecira) [29]. Area under the curve (AUC) measurement across 120 min was determined from the average for each animal, using the trapezoidal method with baseline set as the blood glucose levels at 0 min.Determination of Airway HyperresponsivenessAirway hyperresponsiveness was examined on P21 and P150. The tested mice were put into the whole-body plethysmograph (EMKA Technologies, Paris, France). Mice were exposed to aerosolized saline (for the baseline measurement) and increasing concentrations of methacholine (3.125, 6.25, 12.5, 25, 50 mg/ml) for 3 min each. Data were recorded and averaged for 5 min after 2 min rest. The index of airflow obstruction was expressed as enhanced pause (Penh, dimensionless parameter), which correlates with pulmonary airflow resistance. Penh is a dimensionless value that represents a function of the ratio of peak expiratory flow (PEF) to peak inspiratory flow (PIF) and a function of the timing of expiration (Pause) (Penh = PEP/PIF6Pause). Penh was calculated based on the EMKA Datanalyst provided by EMKA Technologies.BALF AssaysMice were anesthetized with 10 chloral hydrate, exsanguinated and then sacrificed. The trachea was cannulated and bronchoalveolar lavage fluid (BALF) was collected by three injections of 0.5 ml phosphate-buffered saline (PBS) into lungs. Total BALF cells were collected by centrifugation, treated with red blood lysis buffer to remove the red blood cells and counted by microscopy using cell counter. Classified cells were performed with Wright iemsa, and then counted on a total of 200 cells under immersion oil at61,000 magnification. The remaining lavage fluid was centrifuged at 1500 r/min for 10 min and the collected 
supernatant was analyzed for cytokine TNF-a.Materials and Methods Ethics StatementAll animal studies were performed in accordance with the Guide for the Care and Use of Laboratory Animals of the National Institutes of Health. All animals care and experimental protocols were approved by the Ethical Principles in Animal Research adopted by the Chongqing Medical University for Animal Experimentation.Neonatal Overfeeding and Airway ResponsivenessHistological AnalysisThe left 12926553 lungs were fixed in 4 paraformaldehyde at least for 72 h,dehydrated in graded alcohol series, cleared with dimethylbenzene, and embedded in paraffin. Serial sections of 5 mm thickness were stained with hematoxylin-eosin (H E). Lung fibrosis was evaluated by Masson staining for collagen accumulation according to the manufacture’s protocols. Bronchi and lung alveoli were evaluated under a Nikon Eclipse E200 microscope adapted to a Nikon Coolpix 995 camera. Total inflammatory cell counts were determined from these images at 400.
