Pearl millet is a major cereal in the arid and semiarid regions of Asia and Africa. It is primarily cultivated for grain production, but its stover is also valued as dry fodder. Pearl millet is resilient to climate change due to its inherent adaptability to drought and high temperatures. It is also tolerant of saline and acid soils, and is well adapted to marginal lands with low productivity. Pearl millet germplasm exhibits large genetic variability for yield components; and various agronomic, adaptation and nutritional traits. Open pollinated varieties and hybrids are two important cultivar options, but higher productivity is realized through hybrids. Pearl millet has fewer pest and disease problems compared to other cereals and is suited to different cropping systems. It is highly responsive to improved crop management practices, as witnessed in parts of India where it is grown as an irrigated summer crop that produces higher yields and better quality grain. Pearl millet has high nutritional value in terms of high levels of energy, dietary fibre, proteins with a balanced amino acid profile, many essential minerals, some vitamins, and antioxidants. These play a significant role in prevention of important human ailments such as diabetes, cancer, cardiovascular and neurodegenerative diseases. There is great potential for harnessing these positive attributes through genetic improvement, improved crop management, and grain processing and food products technologies. These should help to develop greater global awareness of the importance of this crop for food and nutritional security.
Neurodegenerative diseases characterized by the presence of α-synuclein-a hallmark of pathologic inclusions termed Lewy bodies-include Parkinson's disease, dementia with Lewy bodies, and multiple-system atrophy. Although motor symptoms are related to the altered presynaptic dopaminergic function in these diseases, the appearance of α-synuclein inclusions precedes the involvement of the nigrostriatal dopaminergic pathway. Hence, the most accurate and earliest definition of premotor Parkinson's disease ought to rely on imaging α-synuclein rather than dopaminergic changes. Moreover, dopaminergic imaging has been controversial in monitoring the effects of investigational disease-modifying drugs. For these clinical trials, intense interest in longitudinally imaging α-synuclein as the primary pathologic process has led to efforts toward developing a suitable radiotracer for this key protein. An overview of the present α-synuclein radiotracer development scenario is presented here.
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