Analysis of Genetic Variation among Populations of Withania somnifera (L.) in South India based on RAPD Markers.

Aim: The present study was carried out to analyze the genetic variations among 20 different populations of Withania somnifera (L.) Dunal collected from different habitats (locations) by RAPD analysis. Methodology: DNA was isolated from the fresh leaf samples collected from the field by Bernatsky and Tankley method. Isolated genomic DNA was purified by phenol: chloroform: isoamyl alcohol (25:24:1) extraction mixture and then amplified by MJ themal cycler. Amplified DNA products were quantified and then subjected to RAPD analysis by the method of Williams et al. Results: Randomly amplified polymorphic DNA (RAPD) was used to analyze the genetic variation and relationship among 20 populations of Withania somnifera collected from different part of South India, including the states of Tamilnadu, Puducherry, Kerala, Andhra Pradesh, Karnataka, Gujarat, Maharashtra and supplemented by two commercial varieties from Uttar Pradesh and Delhi. Out of 40 primers, 11 selected primers produced 96 consistent RAPD markers ranging in size from 0.2 kb to 4.0 kb; out of which 75 were polymorphic. Similarity indices were estimated using the Dice coefficient of similarity and cluster analyses were carried out on the similarity estimates using the unweighted pairgroup method to produce a dendrogram using arithmetic average (UPGMA) in the NTSYSpc-verson 1.80 software. The similarity coefficient ranges from 0.53 to 0.98, suggesting that the pronounced genetic variations exist among populations of W. somnifera in South India. The cluster analysis indicates that the 20 populations of W. somnifera were divided into five major groups, regardless of geographical locations. Conclusion: The RAPD analysis indicates existence of genetic variations in natural populations and it may influence and produce changes in phytochemical constituents of W. somnifera populations.

Prediction of tubulo-interstitial injury by Doppler ultrasound in glomerular diseases: value of resistive and atrophic indices.

BACKGROUND: Doppler ultrasound is increasingly used in Nephrology for diagnosis of renovascular hypertension and evaluation of allograft dysfunction. However, its utility in glomerular disease remains controversial. OBJECTIVES: Using Doppler Ultrasound, we prospectively tested the role of resistive and atrophic indices in predicting tubulointerstitial lesions in patients with glomerular disease as demonstrated by renal biopsy. METHODS: Seventy one patients with primary or secondary glomerular diseases were examined by Doppler ultrasonography immediately before renalbiopsy. The resistive and atrophic indices (RI & AI) were calculated and compared with histologic changes in biopsy specimen. RESULTS: Receiver Operator Characteristics analysis showed RI of 0.60 as an optimal value for discriminating tubulointerstitial changes with sensitivity of 82.7% and specificity of 92%. An AI of 0.65 was shown to be optimal for discriminating tubulointerstitial injury with sensitivity of 69.2% and specificity of 85%. The combination of the two indices had not been found to be superior to either index alone. There was a significant correlation between atrophic and resistive indices. (r=0.358, p< 0.01). It was observed that older age, smoking, elevated AI and RI, low GFR, high serum cholesterol and Hypertension were found to be significantly associated with the presence of tubulointerstitial injury in the univariate analysis whereas only elevated AI and RI were found to predict tubulointerstitial injury in multivariate analysis. CONCLUSION: Measurement of RI by Doppler ultrasound can be considered as a supplementary diagnostic tool in glomerular diseases to predict the severity of tubulointerstitial injury.

Specific activities of seminal vesicular phosphomonoesterases and Mg2+-,Ca2+- and Na+/K(+)-adenosine triphosphatases in hypo- and hyperthyroid albino rats.

Hypothyroidism (surgical thyroidectomy) inhibited the activities of acid phosphatase and Mg(2+)-ATPase in seminal vesicular tissue and fluid and that of Ca(2+)- and Na+/K(+)-ATPases in fluid alone, and T4 supplementation restored normalcy in all, except acid phosphatase. Hyperthyroidism (T4 25 micrograms/100g body weight/day for 60 days, im) enhanced the activities of alkaline phosphatase and ATPases in seminal vesicular tissue and fluid, and decreased acid phosphatase activity in tissue alone. Withdrawal of T4 treatment from hyperthyroid rats (after 30 days) augmented the activity of ATPases in tissue and impaired the same in fluid, while phosphomonoesterases remained at hyperthyroid level. The results suggest specific responses of various seminal vesicular phosphatases to altered thyroid hormone status. Modification in the specific threshold of androgen/estrogen action on different phosphatases in seminal vesicles appears to be the plausible mechanism underlying these changes in hypo- and hyperthyroid conditions.