G.V. Venkataramana, Sreenivasa, Azis, K. Fauzie, Amruta Nori-Sarma, and Michelle Bell
G.V. Venkataramana, Sreenivasa, Azis, K. Fauzie, Amruta Nori-Sarma, and Michelle Bell
G.V. Venkataramana, Sreenivasa, Azis, K. Fauzie, Amruta Nori-Sarma, and Michelle Bell
ABSTRACT
Introduction: Traffic is a major contributor to air pollution in Indian cities, and traffic-related Results: DLS and EDX analysis found that roadside PM was mainly fine particles (PM2.5) and
exposure has been shown to induce acute inflammation in humans, both in chamber studies consists of 56% black carbon that generated mostly from vehicular emissions. The samples
using diesel exhaust and in real-life environments such as road traffics. In urban centers, also contain trace metal elements like Si, Fe, Ca, Al, Na and K. There was a significant
diesel exhaust particles are considered to be the hazardous pollutants released from reduction of the bronchoalveolar lavage lymphocyte cell numbers (8.75) after 30 and 90 days
automotive engines due to their aerodynamic and chemical characteristics. exposure. This inflammation has elevated expression of neutrophils, monocytes and
eosinophils compare to control. Percentage viability of leucocytes has decreased and
Methods: Elemental composition and size distribution of particulate matter (PM) were differential cell of macrophages and neutrophils were increased in BAL fluid following mice
analyzed using Energy Dispersive X-Ray (EDX) and Dynamic Light Scattering (DLS) method, exposure to PM2.5 in different intervals.
respectively. Preparation of BAL was done following Harrod’s protocol with some
modifications (Harrod et al., 1998). The mice were exposed to particulate pollution for Conclusions: The exposure to the mixture of suspended particulate matter particles induces
5,15,21,30 and 90 days (each 6 hours/day) in inhalation chambers placed 2.5 m from a street pathological changes, differential cell counts and inflammatory response in the lungs of mice
with heavy traffic in Mysore city. Total and differential cell count and viability were determined in a dose and duration dependent pattern. The responses observed from the present study
using an improved Nebur’s hemocytometer and optical microscope with a 400x zoom. are associated with the bioavailability of inhaled particulate mixtures.
INTRODUCTION
• Air pollution is an emerging biggest public health threat in developing countries especially in India and China.
• As per recent estimates around 4·2 million deaths globally were attributed to long-term air pollution exposures, which represent 7·6% of total global mortality.
• Air pollutants have direct effect on cardiopulmonary health. Several studies worldwide have reported that exposures to ambient air pollution accelerates lung function decline in adults and
increase risk for COPD; impairs lung development in children; significantly increases risk for cardiovascular diseases. Additionally, recent reports also suggest causal role of air pollution in
obesity, metabolic syndrome and diabetes, which is growing to an epidemic proportion in India.
• Air pollution levels in major Indian cities are 2-5 times higher than Western world. In urban settings, automobile emission followed by industrial emission are the major contributors of PM.
• Although air pollution exposures are linked with adverse respiratory health, the key components of PM and underlying cellular and molecular mechanism are not well understood. Our long-
term goal is to identify the key components in particulate matter that elicits toxic responses and eventually leads to lung injury.
• This study was conducted in Mysore city located 135 Km south of Bangalore, Karnataka, India. Mysore is a moderate size city with 128 sq Km area and approximately 1 million people. As
per the Government of India, Mysore city was awarded as cleanest city in India in 2014-2015. Despite being tagged as a clean city, the levels of PM2.5 ranged from 25-30 ug/m3. We carried
this study to characterize the composition of Mysore PM and its effect on pulmonary inflammation in mouse models.
RESULTS
EDX analysis found that ambient particulate matter collected from roadside sampling site Fig. 3 shows sparse, mild foci of macrophages (A) represents alveolar parenchyma in 30 days
consists of 56.38% carbon, 33.66% oxygen, and other elements in smaller fraction such as exposed mice. Alveolar spaces (B) are enlarged, hypertrophy and irregular (a and b) in lung
silicon, iron, aluminium, calcium, sodium, and potassium (Fig. 1). Maximum number of parenchyma of 90 days exposed mice. Accumulation of particles within alveolar macrophages
particles suspended in the DLS sample container has aerodynamic diameter of 318 nm (Fig. was readily apparent in lung parenchyma (C) and in lymph nodes (D) of 90 days exposed
2). Peak summary report from DLS analysis also indicates that 97.4% of the total sample mice. There was a significant variation of BAL cell counts after 30 and 90 days exposure; this
volume contains particles with an average diameter of 275.8 nm. inflammation has elevated the expression of neutrophils and macrophages (Table 1).
A B b Table 1
C D
Acknowledgements
We thank University Grants Commission (UGC) for awarding Raman Postdoctoral Fellowship to VGV and acknowledge funding from Science and Engineering Research Board (SERB),
Department of Science and Technology.