Caffeine Modulates Hyperoxia - Induced Angiogenesis in Newborn Mice

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Caffeine Modulates Hyperoxia - Induced Angiogenesis in Newborn Mice Vikramaditya Dumpa, MD Lori C Nielsen, MS Huamei Wang, MD Vasanth HS Kumar, MD Supported by AAP Marshall Klaus Perinatal Research Grant

I have no relevant financial relationships with the manufacturer(s) of any commercial product(s) and/or provider(s) of commercial services discussed in this CME activity

Caffeine therapy for Apnea of Prematurity (CAP) Trial Caffeine reduces BPD when used within the first 10 days in preterm infants < 1250 grams (Schimdt,B et al N Engl J Med, 2006) The administration of positive airway pressure through an endotracheal tube, the use of any positive airway pressure, and oxygen therapy were each discontinued one week earlier for infants in the caffeine group than for infants in the placebo group (Schimdt,B et al N Engl J Med, 2006) Reduced duration of mechanical ventilation vs. Direct pulmonary effect of caffeine

Possible mechanisms of actions of caffeine Caffeine decreases the pulmonary tissue expression of chemokines & leukocyte influx following hyperoxia in newborn mice (Weichelt,U et al Eur Respir J 2013) Caffeine promotes anti-inflammatory effects in the immature lung of prenatal LPS-exposed rat pups, associated with improvement of respiratory system resistance (Koroglu,O et al Neonatology 2014) Caffeine induces alveolar apoptosis in the hyperoxia-exposed developing mouse lung (Dayanim,S et al Pediatr Res 2014)

Dysregulated angiogenesis Hallmark of BPD Bhandari, A et al Pediatrics 2009

Normoxia / Hyperoxia Role of HIF in Lung Development PHD Complex O 2 HIF-1α-OH Proteosomal Degradation Hypoxia HIF-1α Expression of genes responsible for angiogenesis / alveolar growth HIF-1?BPD HIF-1β HIF-1α HRE Expression of HIF regulated genes VEGF and its receptors / HO-1 / Angiopoietin 1 / Angiopoietin 2 Nucleus Normal lung growth & function

Normoxia / Hyperoxia Does Caffeine Modulate HIF Expression and Regulation? PHD Complex O 2 HIF-1α-OH Proteosomal Degradation Hypoxia HIF-1α Expression of genes responsible for angiogenesis / alveolar growth HIF-1?BPD HIF-1β HIF-1α HRE Expression of HIF regulated genes VEGF and its receptors / HO-1 / Angiopoietin 1 / Angiopoietin 2 Nucleus Normal lung growth & function

Hypothesis HIF Angiogenesis / Growth Factors Microvascular growth drives alveolar / Lung growth We hypothesize that caffeine modulates HIF / angiogenic gene expression to attenuate BPD

Objectives To study the effects of caffeine on gene expression in hyperoxia induced lung injury in newborn mice. The following genes are studied, Hypoxia inducible factors (HIF-1α, HIF-2α, HIF-3α &HIF-1β) VEGF & its receptors (VEGFR1) Prolyl hydroxylase-2 (PHD-2) To study the effects of caffeine on histopathology and alveolization in adult mice

Study Design Treatment Groups (C57/BL6 strain mice; n= 6 in each group) 1. Room Air + Normal saline (RA-NS) 2. RA + Caffeine (RA-CAF) 3. O 2 + NS (O 2 -NS) 4. O 2 + Caffeine (O 2 -CAF) 95% O 2 or RA P5 P0 Caffeine citrate 20mg/kg/day IP injections qd X 5 days P4 Postnatal Day Sacrifice mrna expression of a. HIF 1α,HIF 2α,HIF 3α,HIF 1β b. VEGF and VEGFR1 c. PHD2 Proteins ( to be assayed)

Molecular studies mrna expression in the lung tissue was analyzed by qrt PCR (Quantified by 2- C(t) method) Data were analyzed on PCR array online web portal (SA Biosciences, MD) P values were calculated based on students T test from the 2- C(t) values for each gene in the control group (room air) and the treatment group (oxygen with and without caffeine) Results are expressed as fold change in mrna expression compared to RA-NS group (p<0.05 considered significant)

Hyperoxia Increases HIF-1α mrna Expression in the Lung 4 HIF 1α Fold change in gene expression Compared to RA NS 3 2 1 0 * *p <0.05 vs. RA NS RA NS RA CAF O2 NS O2 CAF

Caffeine or Hyperoxia by Itself Increases mrna Expression of HIF-2α,HIF-3α, HIF-1β and VEGF

Fold change in gene expression compared to RA NS 3.5 3 2.5 2 1.5 1 0.5 Caffeine or Hyperoxia by Itself Increases VEGFR1 mrna Expression in the Lung VEGFR1 * * *p <0.05 vs. RA NS 0

Caffeine by Itself Increases PHD-2 mrna Expression in the Lung Prolyl Hydroxylase 2 3.5 Fold change in gene expression compared to RA NS 3 2.5 2 1.5 1 0.5 * *p<0.05 vs. RA NS 0

Angiogenic mrna Expression HIF-1α HIF-2α HIF-3α CAFFEINE HYPEROXIA CAFFEINE + HYPEROXIA Expression Similar to RA HIF-1β VEGF VEGFR1 PHD-2

Conclusions Caffeine in room air, produces transcriptional changes in HIF gene expression resulting in increased angiogenic mrna expression Exposure to hyperoxia alone causes increased angiogenic mrna expression, possibly leading to dysregulated angiogenesis Caffeine reverses the hyperoxia induced changes in HIF expression and other angiogenic genes in the lung, to that comparable to the room air group.

Histopathology Treatment Groups (C57/BL6 strain mice; n= 6 in each group) Room Air + Normal saline (RA-NS) RA + Caffeine (RA-CAF) O 2 + NS (O 2 -NS) O 2 + Caffeine (O 2 -CAF) 95% O 2 or RA RA P0 Caffeine 20mg/kg/day P5 12 Weeks IP injections; qd X 5 days Postnatal Day Molecular Studies (HIF / Angiogenesis) Protein Expression Pending Histopathology Quantification RAC / MLI

Lung Histopathology in 12 Week Mice Trachea was cannulated and the lungs were inflation fixed with 10% formalin at 25 cm H 2 O pressure Lung sections stained with H&E for assessment of alveolization and lung morphometry Morphometric analysis was performed by Radial alveolar count (RAC) and Mean linear intercept (Lm)

Hyperoxia decreases alveolization, however caffeine may be protective to the lung RA NS 10X MAGNIFICATION RA CAF O2 NS O2 CAF

Hyperoxia decreases alveolization, however caffeine may be protective to the lung RA NS 40X MAGNIFICATION RA CAF O2 NS O2 CAF

Radial Alveolar Count H & E Staining of formalin fixed lung sections Alveolization Radial alveolar count Images captured on Aperio Imaging software (Leica Biosystems, Buffalo Grove, IL) Postnatal lung growth was assessed by Radial Alveolar Count of Emery & Mithal, which assesses the complexity of the terminal respiratory unit (Arch Dis Child 1960;35:544-7)

Caffeine Enhances Alveolization In The Presence Of Hyperoxia As Measured By Radial Alveolar Count 16 *p <0.05 vs. other 3 groups Radial Alveolar Count 12 8 4 * 0 RA NS RA CAF O2 NS O2 CAF

Mean Linear Intercept Images from H & E staining of lung sections were captured on Aperio Imaging software (Leica Biosystems, Buffalo Grove, IL) Mean linear intercept (Lm), an indicator of mean alveolar distension, was assessed in 20 nonoverlapping fields of lung parenchyma per animal at 40 magnification in digitalized images

Caffeine Decreases Hyperoxia Induced Air Space Enlargement Lm (µm) 100 80 60 *p <0.05 vs. other 3 groups * 40 20 0 RA NS RA CAF O2 NS O2 CAF

Conclusions Exposure to neonatal hyperoxia leads to impaired alveolization as suggested by lower RAC and airspace enlargement demonstrated by higher Lm Addition of Caffeine in the newborn period during hyperoxia exposure significantly improves alveolization with an absence of air space enlargement This may suggest that caffeine may have a lung protective effect in the neonatal period in the presence of hyperoxia

Speculation The lung protective effect of caffeine in improving alveolization may be related to microvascular growth in the newborn period leading to improved alveolar growth. Similar mrna expression with room air caffeine and hyperoxia groups resulting in different alveolization patterns needs to be explored further. Caffeine may modulate HIF-1 signaling pathway & hence regulate the angiogenic gene expression in the presence of oxygen, to promote normal vascular and alveolar growth in the lung, thereby decreasing BPD.

THANK YOU

Caffeine Dosing 20 mg/kg caffeine in mice translates to a dose of 2.4 mg/kg in humans. Nonetheless, gene expression changes are noted at relatively low doses of caffeine in mice. Reagan Shaw S, The FASEB Journal 2007

Caffeine with Hyperoxia group demonstrate weight gain as Adult Mice Weight at Birth Weight at 12 weeks Weight (grams) Weight (grams) RA-NS 02-NS O2-CAF

Molecular Studies Gene expression in the lung tissue was analyzed by qrt PCR (Quantified by 2- C(t) method; reference genes phosphoglycerate kinase 1 & peptidylprolyl isomerase A) HIF-1α, HIF-2α, HIF-3α and HIF-1β subunits VEGF VEGFR1 Prolyl Hydroxylase-2 Pfaffl, MW et al Nucleic acid research, 2001

Alveolization is similar with or without caffeine in adult mice exposed to room air RA Saline Group 100x RA Caffeine Group 400x

Hyperoxia decreases alveolization, however caffeine may be protective to the lung O2 Saline Group 100x O2 Caffeine Group 400x

Cytokine Measurements The following cytokines were measured in the lung by enzyme immune assay in all the groups TNF α Interferon-γ Interleukin-6

No significant Difference in TNF-α Among the Groups 0.06 RA+S RA+C O2+S O2+C 0.05 pg/µg lung tissue 0.04 0.03 0.02 0.01 0 TNF-α

No significant Difference in Interferon-γ in the Lung Among the Groups 0.2 RA+S RA+C O2+S O2+C pg/µg lung tissue 0.16 0.12 0.08 0.04 0 Interferon γ

No significant Difference in IL-6 in the Lung Among the Groups 0.16 RA+S RA+C O2+S O2+C pg/µg lung tissue 0.12 0.08 0.04 0 Interleukin 6 (IL 6)