مولانا امتیاز علی خان عرشی
۲۴؍ ۲۵؍ فروری ۱۹۸۱ء کی درمیانی شب میں مولانا امتیاز علی خان عرشی کا حرکتِ قلب بند ہوجانے سے رام پور میں انتقال ہوگیا، اناﷲ وانا الیہ راجعون۔ وہ ممتاز اہل قلم، غالبیات کے ماہر اور رضا لائبریری رام پور کے ڈائرکٹر تھے، ان کی وفات علمی دنیا کا بڑا حادثہ ہے۔
عرشی صاحب کا خاندنی تعلق افغانستان کے یوسف زئی قبیلہ کی ایک شاخ حاجی خیل سے تھا، ان کے دادا مولانا اکبر علی خان محدث پیشہ آباسپہ گری چھوڑ کر علم و فضل کے کوچہ میں وارد ہوئے، ان کی علمی جانشینی ان کے ایک فرزند مولانا جعفر علی خاں کے حصہ میں آئی، اور سب سے چھوٹے صاحبزادے مختار علی خاں صاحب کی کم سنی ہی میں ان کا انتقال ہوگیا، اس لیے یہ تعلیم کا سلسلہ جاری نہ رکھ سکے، مگر ان ہی کے صاحبزادے مولانا امتیاز علی خان عرشی اس خاندان کے گل سرسبد ہوئے۔
امتیاز علی خان صاحب کی پیدائش ۸؍ دسمبر ۱۹۰۴ء کو ہوئی، انھوں نے ابتدائی تعلیم گھر پر حاصل کرنے کے بعد عربی قواعد اور فارسی کی درسی کتابیں مدرسہ مطلع العلوم میں پڑھیں اس زمانہ میں پنجاب یونیورسٹی کے مشرقی امتحانات کا بڑا چرچا تھا، ہونہار طلبہ ملک کے گوشہ گوشہ سے امتحانات دینے کے لیے لاہور جاتے تھے، عرشی صاحب نے ۱۹۲۳ء میں مولوی اور عالم کے امتحانات میں اول درجہ میں کامیابی حاصل کی، اس کے بعد مولوی فاضل کے امتحان کی تیاری کے لیے اورنٹیل کالج لاہور میں داخلہ لیا، یہاں مولانا نجم الدین، مولانا سید طلحہ اور مولانا عبدالعزیز میمن جیسے ہندوستان گیر شہرت رکھنے والے استاذوں کا طوطی بول رہا تھا، مولانا سید طلحہ کا تعلق حضرت سید احمد شہید بریلویؒ کے دودمانِ عالی سے تھا، عرشی صاحب کا خاندان سید صاحبؒ کا معتقد اور رام...
It is with great pleasure that I write this editorial to welcome you to the first issue of this new International journal, “Pakistan Biomedical Journal” (PBMJ). The topics covered by the journal are certainly broad and interesting. Biomedical science is a collection of applied sciences that help us understand, research, and innovate within the field of healthcare. It includes disciplines like molecular biology, clinical virology, bioinformatics, and biomedical engineering, among others. It's designed to apply the biological sciences to advance not only individual health but also the area of public health. Biomedical Research can help health professions better understand things like the human body and cell biology, making advances in our understanding of epidemics, health initiatives, and human health in the age of longer life expectancy. It aids our understanding of infectious disease and provides research opportunities into some of our most troubling health issues. The journal will continue to publish high quality clinical and biomedical research in health and disease later in life. Peer review will remain a vital component of our assessment of submitted articles.I am very happy to have a team of excellent editors and editorial board members from the top international league covering in depth the related topics. They will ensure the highest standards of quality for the published manuscripts and, at the same time, keep the process time as short as possible. We hope to bring best researches in the field of biomedical sciences that may serve as a guideline in health awareness, understanding the mechanisms and its management in future. We definitely look forward to receiving your excellent studies to making PBMJ synonymous with high quality in the biomedical science domain.
Alzheimer‟s disease (AD) is the most common neurodegenerative disorder, characterized by memory impairment, behavioral turbulence, cognitive dysfunction and imperfection in routine life activities. AD is the most common cause of dementia among people aged 65 years and older, with about 35 million sufferers worldwide. It is the fifth leading cause of death in people above 65 years of age and is predicted to affect 1 in 85 people globally by 2050. The most important pathological aspects of AD include deficiency of neurotransmitter acetylcholine, deposition of amyloid plaques (Aβ) and neurofibrillary tangles. Cancer is another life-threatening disease and serious health problem worldwide. More than half of the 20 million people diagnosed with cancer belong to the developing regions of the world. Due to the alarming increase in cancer incidences, it is estimated to have 10 million deaths annually by 2020. Natural products play a significant role in the drug discovery and development process. The main advantage of natural products as a source of lead compounds is the tremendous molecular diversity found in nature. Based on the folkloric uses of P. hydropiper and related species, we investigated solvent extracts, essential oils and isolated compounds for anti-Alzheimer''s and cytotoxic potentials by using in-vitro and in-vivo models. A total of seven fractions were derived from the dried whole plant of P. hydropiper using solvent-solvent extraction method. Essential oils from leaves and flowers were also isolated and subjected to Gas Chromatography-Mass Spectrometry (GC-MS) analysis. Crude methanolic extract (Ph.Cr) was subjected to qualitative phytochemical analysis, GC-MS analysis and column chromatography for isolation of bioactive compounds. Ph.Cr was tested positive for the presence of alkaloids, flavonoids, saponins, tannins, triterpenoids anthraquinones, glycosides. In GC-MS analysis of Ph.Cr, n-hexane (Ph.Hex), chloroform (Ph.Chf), butanol (Ph.Bt) and ethyl acetate (Ph.EtAc) fractions 126, 124, 181, 131 and 164 compounds were identified respectively. In acetylcholinesterase (AChE) inhibition assay, Ph.Hex , Ph.Chf and Ph.Sp were the most potent fractions that displayed IC50 values of 35, 55 and 100 μg/ml respectively. While in butyrylcholinesterase (BChE) inhibition assay, Ph.Aq and Ph.Hex were more potent with IC50 values of 3 and 40 μg/ml respectively. In DPPH free radicals scavenging assay, Ph.Bt, Ph.Chf, Ph.EtAc, Ph.Lo and Ph.Fo fractions were more potent among all samples with IC50 of 3, 10, 15, 20 and 200 μg/ml respectively. In ABTS anti-radicals assay, Ph.Bt, Ph.EtAc, Ph.Aq, Ph.Sp revealed highest ABTS scavenging effect, thus causing IC50 values91.03, 90.65, 90.56 and 90.84% inhibition of free radicals respectively. From the most active fraction including chloroform and ethyl acetate six compounds (MA1-6) were isolated , purified and their structures were confirmed by 1H NMR, 13C NMR and mass spectra. The most potent compound MA-1 and Ph.Lo were subjected to in-vivo anti-Alzheimer and cell line studies. In AChE inhibition assay, MA-1 exhibited IC50 of 55 μg/ml, whereas, in BChE inhibitory assay MA-1 showed IC50 of 50 μg/ml. Likewise Ph.Lo and Ph.Fo demonstrated IC50''s of 120 and 220 μg/ml respectively in AChE inhibition assay. In BChE inhibitory study, Ph.Lo and Ph.Fo showed IC50''s of 130 and 225 μg/ml respectively. In DPPH, ABTS, H2O2 anti-radicals assays, MA-1 exhibited IC50''s of 140, 120 and 280 μg/ml respectively. Whereas, Ph.Lo and Ph.Fo displayed IC50''s of 180 and 45 μg/ml respectively. Moreover, the IC50''s were 60 and 50 μg/ml for Ph.Lo and Ph.Fo respectively in H2O2 radicals scavenging assay. In beta amyloid cleaving enzyme (BACE1) inhibition assay, MA-1 and Ph.Lo displayed 73.00 ± 3.05 and 79.33 ± 3.17% enzyme inhibition respectively at 1 mg/ml concentration. In trasgenic animals model of Alzheimer disease MA-1 and Ph.Lo showed significant decline in cognitive dysfunctions of animals evaluated through behavioral assessment tools including Paddling water Maze (PWM), Y-Maze, open field and balance beam. Ex-vivo studies suggested that MA-1 and Ph.Lo sufficiently cross blood brain barier (BBB) and treated transgenic animals with these samples showed a significant decline in the AChE, BChE activities in the cortical and hippocampus tissues. Moreover, the cortical and hippocampus tissues of transgenic animals treated with MA-1 and Ph.Lo exhibitied a significant DPPH radicals scavenging effect. In cytotoxicity studies, Ph.Lo was less effective against all tested cell lines with LC50> 1000 μg/ml. MA-1 displayed LD50 of 440, 170, 200 μg/ml against NIH/3T3, HeLa and MCF-7 cell lines. Moreover, compound MA-3 displayed LD50 of170, 60 and 140 μg/ml against HeLA, MCF-7 and NIH/3T3 cell lines respectively. Whereas, compound MA-4 demonstrated 380, 160 and 58 140 μg/ml against HeLA, MCF-7 and NIH/3T3 cell lines respectively. Concluding the current study, it is stated that P. hydropiper crude extracts and isolated compounds possess considerable neuroprotective and selective cytotoxic potentials. Further studies are required regarding their potential use in Alzheimer disease and cancer.