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Breathing insights: Biomarkers as tools for chronic obstructive pulmonary disease assessment - A systematic review. 呼吸洞察:作为慢性阻塞性肺疾病评估工具的生物标志物-系统综述。
IF 1.5 4区 医学 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2026-01-01 Epub Date: 2026-01-07 DOI: 10.4103/ijp.ijp_970_24
Sonali Singh, Atul Kabra, Pradeep Goyal

Abstract: Chronic obstructive pulmonary disease (COPD) remains a major global health burden, posing ongoing challenges in diagnosis and management. This systematic review examines current evidence on biomarkers relevant to COPD, emphasizing their diagnostic, prognostic, and therapeutic potential. A comprehensive search of PubMed and Scopus identified studies published from January 2019 to April 2025 involving adult COPD patients. Two independent reviewers screened observational and randomized studies, with duplicates (n = 24) removed using Mendeley and verified manually. Due to heterogeneity in methodology and outcomes, data were synthesized narratively. Risk of bias was assessed using RoB 2.0 for randomized trials and the Newcastle-Ottawa Scale for observational studies. Traditional biomarkers such as C-reactive protein and fibrinogen were consistently associated with exacerbation risk and disease severity. Interleukins-6 and -8 were elevated in frequent exacerbators, while surfactant proteins showed potential in distinguishing COPD from other chronic lung diseases. Emerging genetic and multiomics markers - such as matrix metalloproteinase-9, chitinase-3-like protein 1, and various microRNAs - demonstrated associations with disease phenotypes and treatment response. The findings highlight that while individual biomarkers offer valuable insights, a combined multimarker approach integrated with clinical parameters may enhance the precision of COPD management. This review provides clinicians and researchers with an updated perspective on the utility and limitations of current biomarkers, supporting the move toward more personalized and effective strategies in COPD care.

慢性阻塞性肺疾病(COPD)仍然是全球主要的健康负担,在诊断和管理方面提出了持续的挑战。本系统综述检查了与COPD相关的生物标志物的现有证据,强调了它们的诊断、预后和治疗潜力。对PubMed和Scopus的综合搜索确定了2019年1月至2025年4月发表的涉及成年COPD患者的研究。两名独立审稿人筛选了观察性研究和随机研究,使用Mendeley剔除重复研究(n = 24)并手工验证。由于方法和结果的异质性,数据以叙述的方式合成。随机试验采用RoB 2.0评估偏倚风险,观察性研究采用纽卡斯尔-渥太华量表评估偏倚风险。传统的生物标志物如c反应蛋白和纤维蛋白原始终与恶化风险和疾病严重程度相关。白细胞介素-6和-8在频繁加重者中升高,而表面活性剂蛋白在区分COPD与其他慢性肺部疾病方面具有潜力。新出现的遗传和多组学标记——如基质金属蛋白酶-9、几丁质酶-3样蛋白1和各种microrna——证明与疾病表型和治疗反应相关。研究结果强调,虽然单个生物标志物提供了有价值的见解,但结合临床参数的综合多标志物方法可能提高COPD管理的准确性。这篇综述为临床医生和研究人员提供了关于当前生物标志物的效用和局限性的最新观点,支持在COPD治疗中朝着更个性化和更有效的策略发展。
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引用次数: 0
Outer membrane protein LipL21 as a potential candidate against Leptospira interrogans: An in silico prediction. 外膜蛋白LipL21作为抗钩端螺旋体的潜在候选物:一个计算机预测。
IF 1.5 4区 医学 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2026-01-01 Epub Date: 2026-01-07 DOI: 10.4103/ijp.ijp_540_23
Anita Kumari, Devinder Toor

Abstract: Leptospirosis is one of the most widespread zoonotic diseases caused by Leptospira interrogans, characterized by mild febrile illness to severe multiorgan failure. The conventional vaccines against Leptospira have several drawbacks, including short-term immunity and serovar-based protection. The current study focuses on determining the most effective outer membrane protein (OMP) as a potential antigen using various computational approaches in providing protection against leptospirosis, as they are conserved within pathogenic serovars. Out of OmpL1, LipL21, LipL32, and LipL41, the VaxiJen analysis revealed LipL21 to be the most antigenic with a score of 0.7848. The antigenic epitopes of LipL21 were further analyzed using BCPred and MHCPred. It is conserved among all the pathogenic serovars while being absent in nonpathogenic. LipL21 had both B-cell and T-cell epitopes, suggesting that it is immunogenic. The VaxiJen score, localization of protein, Clustal Omega, and confirmational analysis of B-cell epitopes were studied for defining a better immunogenic and conserved OMP. This study holds importance as the surface proteins are a potential vaccine candidate for the development of new and effective vaccines in the prevention of leptospirosis hold. An ideal protein, which has its entire conserved immunogenic domain, would confer cross-protection against heterologous serovars. Thus, using bioinformatic approaches, we for the first time predict that LipL21 is a promising, effective vaccine candidate in providing protection against Leptospira.

摘要钩端螺旋体病是由钩端螺旋体引起的一种分布最广的人畜共患疾病,其特征为轻度发热到重度多器官功能衰竭。传统的钩端螺旋体疫苗有几个缺点,包括短期免疫和基于血清的保护。目前的研究重点是使用各种计算方法确定最有效的外膜蛋白(OMP)作为潜在抗原,以提供对钩端螺旋体病的保护,因为它们在致病性血清型中是保守的。在OmpL1、LipL21、LipL32和LipL41中,VaxiJen分析显示LipL21的抗原性最高,得分为0.7848。利用BCPred和MHCPred进一步分析LipL21的抗原表位。它在所有致病性血清型中都是保守的,而在非致病性血清型中则不存在。LipL21同时具有b细胞和t细胞表位,表明它具有免疫原性。研究了VaxiJen评分、蛋白定位、Clustal Omega和b细胞表位的确认分析,以确定更好的免疫原性和保守的OMP。该研究具有重要意义,因为表面蛋白是开发新的有效预防钩端螺旋体病疫苗的潜在候选疫苗。一个理想的蛋白,具有其整个保守的免疫原结构域,将赋予对异源血清型的交叉保护。因此,利用生物信息学方法,我们首次预测LipL21是一种有希望的、有效的钩端螺旋体保护候选疫苗。
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引用次数: 0
Telemedicine and digital health: The future for pharmaceutical companies and health care. 远程医疗和数字健康:制药公司和医疗保健的未来。
IF 1.5 4区 医学 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2026-01-01 Epub Date: 2026-01-07 DOI: 10.4103/ijp.ijp_452_24
Pathan Azher Khan, Payal Jayendra Badole, Darakshan Shaikh

Abstract: In today's fast-paced world, demand for convenient patient care is high, prompting the rise of telemedicine and digital health platforms. These platforms offer quick solutions for health management, aligning with the trend of utilizing online tools for various needs. Integrating these technologies into health care ensures top-notch facilities without disrupting busy lifestyles. This review provides a comprehensive view of their benefits, enhancing patient access and streamlining processes. The paper explores diverse applications such as electronic health records and mobile health apps, empowering patients and enabling real-time decision-making for healthcare providers. It emphasizes the role of big data analytics in managing vast health-related data. Government initiatives and regulatory frameworks are also discussed. Through case studies, the review illustrates the tangible impact of these technologies on patient outcomes and healthcare efficiency. Embracing digital health and telemedicine is crucial for pharmaceutical stakeholders to adapt to evolving patient needs and drive innovation in modern health care.

摘要:在当今快节奏的世界中,对方便患者护理的需求很高,促使远程医疗和数字健康平台兴起。这些平台为健康管理提供了快速解决方案,顺应了利用在线工具满足各种需求的趋势。将这些技术整合到医疗保健中,确保了一流的设施,而不会扰乱繁忙的生活方式。这篇综述提供了他们的好处,提高患者访问和简化流程的全面观点。本文探讨了各种应用,如电子健康记录和移动健康应用程序,赋予患者权力,使医疗保健提供者能够实时决策。它强调大数据分析在管理大量健康相关数据中的作用。还讨论了政府举措和监管框架。通过案例研究,本文阐述了这些技术对患者治疗结果和医疗效率的切实影响。拥抱数字卫生和远程医疗对于制药利益相关者适应不断变化的患者需求和推动现代卫生保健创新至关重要。
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引用次数: 0
Drug-induced mania and parkinsonism in substance use disorder patient: A case report. 物质使用障碍患者药物性躁狂症和帕金森症1例。
IF 1.5 4区 医学 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2026-01-01 Epub Date: 2026-01-07 DOI: 10.4103/ijp.ijp_1041_24
Ragesh Gurumoorthi, Ramakrishnan Subbaraya Rajendran, Akila Murugan, Karthik Thiyagarajan, Muhasaparur Ganesan Rajanandh

Abstract: This case report investigates mania and parkinsonism induced by olanzapine and disulfiram in a patient with substance use disorder. DSM-5 criteria were used for the diagnosis of drug-induced parkinsonism, and movement disorder severity was assessed with the Simpson-Angus Scale. After initiating olanzapine and disulfiram therapy, the patient developed extrapyramidal symptoms and manic features. Naranjo scale indicated a probable drug reaction (score = 7), while Hartwig Severity Assessment (Level 4) suggested that hospitalization was required and these reactions were nonpreventable. The case underscores the need for vigilant monitoring and tailored treatment in patients with psychiatric conditions.

摘要:本病例报告调查了1例物质使用障碍患者奥氮平和双硫仑所致躁狂症和帕金森病。采用DSM-5标准诊断药物性帕金森病,采用Simpson-Angus量表评估运动障碍严重程度。在开始奥氮平和双硫仑治疗后,患者出现锥体外系症状和躁狂特征。Naranjo量表提示可能存在药物反应(得分= 7),而Hartwig严重程度评估(4级)提示需要住院治疗,这些反应是不可预防的。该病例强调了对精神疾病患者进行警惕监测和量身定制治疗的必要性。
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引用次数: 0
Embracing innovations and upholding excellence in pharmacology. 拥抱创新,坚持卓越的药理。
IF 1.5 4区 医学 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2026-01-01 Epub Date: 2026-01-07 DOI: 10.4103/ijp.ijp_1296_25
Babul Kumar Bezbaruah, Debasish Hota
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引用次数: 0
Inclusion of "palliative care pharmacology" as a new chapter in the pharmacology textbook for medical undergraduate students: A strength, weakness, opportunity, and threat analysis. 将“姑息治疗药理学”作为医学本科生药理学教科书的新章节:优势、劣势、机会和威胁分析。
IF 1.5 4区 医学 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2026-01-01 Epub Date: 2026-01-07 DOI: 10.4103/ijp.ijp_474_24
Aditi Chaturvedi, Sandip Mukhopadhyay, Rangeel Singh Raina, Gurpreet Kaur

Abstract: Palliative care is a multidisciplinary approach aimed at improving the quality of life (QoL) and alleviating sufferings of people with serious and terminal illnesses. The present health system understands that palliative and rehabilitative services offer care to patients when cure is not possible. The concept is relatively new for most Indian graduates due to little emphasis on palliative care in the medical curriculum in India. Although palliative care has been incorporated in Universal Health Coverage in India and now also in the new competency-based medical curriculum in various subjects, including pharmacology, by the National Medical Commission, it is seldom emphasized to medical undergraduates in a structured, separate chapter. Like many other countries, it largely lacks implementation due to a lack of information and emphasis in standard textbooks. Palliative care is considered to be part of the primary healthcare system, and our budding physicians are supposed to be empowered with the prescription skills in palliative care. In the Indian scenario, this is being adopted newly in the medical training of primary care with the new medical education system. Pharmacology plays an important role in understanding the use of palliative care medicines. Palliative care pharmacology includes the use of various medications that target specific symptoms or conditions, for example, opioids such as morphine, fentanyl, and oxycodone for severe pain, antiemetics to alleviate nausea and vomiting, and benzodiazepines to manage anxiety and agitation. Most of the drugs prescribed in palliative care are usually covered in pharmacology textbooks, but in a "piecemeal." However, an explicit chapter on palliative care with the relevant pharmacology helps the young medicos to get sensitized to the drugs and acquire the requisite prescription skills early on the same go. "Strength, weakness, opportunity, and threat analysis" is a tool for strategic planning to assess the intrinsic and extrinsic factors, as well as the existing and upcoming potential of an initiative. Palliative care, which is relatively a new concept for MBBS teaching in India, is still at a primitive stage and needs more emphasis to provide definite advantages with the changing needs of society. Here, in a fresh perspective, through this fact-based analysis we looked at competitive position of 'Pharmacology' discipline to provide the early exposure of 'palliative care' to the MBBS students through a new chapter. We also explored its current relevance and future potential. In addition, we analyzed the internal and external factors influencing this approach, including its strengths, weaknesses, opportunities, and threats.

摘要:姑息治疗是一种多学科的治疗方法,旨在改善严重和晚期疾病患者的生活质量(QoL)和减轻痛苦。目前的卫生系统明白,姑息治疗和康复服务为无法治愈的患者提供护理。对于大多数印度毕业生来说,这个概念相对较新,因为印度的医学课程很少强调姑息治疗。尽管缓和医疗已被纳入印度的全民健康覆盖,现在也被国家医学委员会纳入了以能力为基础的各种学科的新医学课程,包括药理学,但很少在一个结构化的单独章节中向医科本科生强调这一点。像许多其他国家一样,由于标准教科书中缺乏信息和重点,它在很大程度上缺乏实施。姑息治疗被认为是初级医疗保健系统的一部分,我们崭露头角的医生应该被赋予姑息治疗的处方技能。在印度的情况下,新的医学教育制度正在初级保健医疗培训中采用这一方法。药理学在理解姑息治疗药物的使用方面起着重要作用。姑息治疗药理学包括使用针对特定症状或病症的各种药物,例如,吗啡、芬太尼和羟考酮等阿片类药物用于治疗剧烈疼痛,止吐剂用于缓解恶心和呕吐,苯二氮卓类药物用于控制焦虑和躁动。姑息治疗中开出的大多数药物通常都包含在药理学教科书中,但都是“零敲碎打”的。然而,关于姑息治疗的明确章节与相关药理学帮助年轻的医生对药物敏感,并尽早获得必要的处方技能。“优势、劣势、机会和威胁分析”是战略规划的工具,用于评估内在和外在因素,以及计划的现有和即将到来的潜力。姑息治疗在印度MBBS教学中是一个相对较新的概念,还处于初级阶段,需要更多的重视,以提供明确的优势,以适应不断变化的社会需求。在这里,通过这个基于事实的分析,我们从一个新的角度来看待“药理学”学科的竞争地位,通过一个新的篇章,为MBBS学生提供“姑息治疗”的早期接触。我们还探讨了其当前的相关性和未来的潜力。此外,我们分析了影响这种方法的内部和外部因素,包括其优势,劣势,机会和威胁。
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引用次数: 0
Carbamazepine-induced aplastic anemia: A rare reported adverse drug reaction. 卡马西平诱导再生障碍性贫血:一种罕见的药物不良反应报道。
IF 1.5 4区 医学 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2026-01-01 Epub Date: 2026-01-07 DOI: 10.4103/ijp.ijp_821_24
Anjali Kushwah, Akhilesh Pratap Singh Tomar, Meghna Shinde, Preeti Acharya

Abstract: Carbamazepine is widely used drug for various neurological psychiatric disorders. Aplastic anemia is its rare serious adverse effect which possess high mortality rate. This is a retrospective case study where aplastic anemia due to carbamazepine was reported. We enquired the case details and on doing the causality assessment by World Health Organization scale, concluded it as a "certain" type of Adverse Drug Reaction (ADR) induced by carbamazepine. A 44-year-old male was taking carbamazepine prescribed for epilepsy for 2 years. For the last 4-5 months, he started having generalized weakness, easy fatiguability, shortness of breath on exertion, and pedal edema. Investigating it, further he was diagnosed with carbamazepine-induced aplastic anemia. Routine blood investigations, bone marrow findings, etiological confirmation done by treating physicians, and reporting of ADRs by pharmacologists through pharmacovigilance program may provide World Health Organization to release drug alerts so as to warrant the future use of culprit drugs.

摘要:卡马西平是一种广泛应用于各种神经精神疾病的药物。再生障碍性贫血是其罕见的严重不良反应,死亡率高。这是一个回顾性的案例研究,其中卡马西平所致再生障碍性贫血的报道。我们对病例进行了详细的调查,并根据世界卫生组织量表进行了因果关系评估,认为是卡马西平引起的“某种”药物不良反应(ADR)。44岁男性,服用卡马西平治疗癫痫2年。在过去的4-5个月里,他开始出现全身无力、易疲劳、用力时呼吸急促和足部水肿。进一步调查后,他被诊断为卡马西平诱发的再生障碍性贫血。常规血液检查、骨髓检查、治疗医生的病因确认以及药理学家通过药物警戒计划报告的不良反应,可能为世界卫生组织发布药物警报提供依据,从而保证今后使用罪魁祸首药物。
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引用次数: 0
A quiet but growing threat: Global perspectives on antifungal resistance and future therapeutic approaches. 一个安静但日益增长的威胁:抗真菌耐药性和未来治疗方法的全球视角。
IF 1.5 4区 医学 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2026-01-01 Epub Date: 2026-01-07 DOI: 10.4103/ijp.ijp_1129_25
Swathi Gurajala, Meera Challapilla

Abstract: Antifungal drug resistance is an escalating global health concern that threatens the effective treatment of fungal infections in both clinical and environmental settings. This review synthesizes developments, focusing on molecular and physiological mechanisms of resistance, key contributing factors, and associated therapeutic limitations. Through selected international case studies over the past 5 years (2020-2025), we illustrate the clinical and ecological consequences of resistant fungal pathogens and emphasize the need for coordinated global responses. We also discuss integrated strategies to mitigate this threat, including strengthened surveillance systems, optimized antifungal stewardship, and advancements in diagnostic tools and therapeutic innovation. By consolidating recent insights and identifying critical research gaps, this review aims to inform future investigations and guide policy frameworks to combat antifungal resistance worldwide.

摘要:抗真菌药物耐药性是一个不断升级的全球健康问题,威胁着真菌感染在临床和环境环境中的有效治疗。本文综述了耐药的分子和生理机制、主要影响因素和相关治疗局限性等方面的研究进展。通过过去5年(2020-2025)选定的国际病例研究,我们说明了耐药真菌病原体的临床和生态后果,并强调了协调全球应对的必要性。我们还讨论了减轻这一威胁的综合策略,包括加强监测系统,优化抗真菌管理,以及诊断工具和治疗创新的进步。通过巩固最近的见解和确定关键的研究差距,本综述旨在为未来的调查提供信息,并指导全球抗真菌耐药性的政策框架。
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引用次数: 0
Cost-effectiveness analysis of intradermal versus classical intramuscular COVID-19 vaccine administration: Specific concern on update situation due to emerging Omicron variant. 皮内注射与经典肌肉注射COVID-19疫苗的成本-效果分析:特别关注新出现的Omicron变体的更新情况。
IF 1.5 4区 医学 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2026-01-01 Epub Date: 2026-01-07 DOI: 10.4103/ijp.ijp_273_22
Pathum Sookaromdee, Viroj Wiwanitkit
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引用次数: 0
Astilbin ameliorates intestinal inflammation and suppresses colorectal cancer cell proliferation by regulating NLRP3 inflammasome and nuclear factor-kappa B signaling pathway. Astilbin通过调节NLRP3炎性体和核因子κ B信号通路,改善肠道炎症,抑制结直肠癌细胞增殖。
IF 1.5 4区 医学 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2026-01-01 Epub Date: 2026-01-07 DOI: 10.4103/ijp.ijp_678_24
Lu Han, Xiao Zhong Deng, Ya Li, Jinqing Hui

Objective: The inflammation-responsive NLRP3 inflammasome and nuclear factor-kappa B (NF-κB) dependent signaling pathways are critically connected with inflammatory conditions and disorders such as colorectal cancer (CRC). Where phytochemicals may be added as preventive natural supplements to control CRC. In this study, we investigated whether astilbin (AST) interacted with anti-inflammatory NLRP3 and NF-κB-dependent molecular events in CRC.

Background: The network of growth signaling redox-sensitive transcription factor NF-κB interacting with the NLRP3 inflammasome in CRC progression needed targeted research. AST is a flavonol reported for anti-inflammatory, immune-suppressive, and antioxidant properties, which are sought to assess CRC growth inhibition through NF-κB and NLRP3.

Methods: AST was applied to HCT116 and HT-29 cells of human origin to examine cell survival, apoptosis, progression, and DNA fragmentation to determine the analysis of gene and protein expression and molecular mechanisms.

Results: AST inhibits the proliferation of HCT116 and HT29, and both cell lines depend on IC50 values of 128 and 144 events. AST caused induction of apoptosis in CRC cells via intrinsic mechanism involving caspase-9 and caspase-3 activation and caused arrest of the G2/M phase cell cycle. AST (100 μm) inhibited colony formation abilities to 54% and wound healing to 62% in both cell lines. In the azoxymethane/dextran sodium sulfate (AOM/DSS)-induced colitis-associated colon cancer mice, the total tumor count was reduced from 14 to 4.3 by the AST 20 mg/kg group, significantly reducing the large tumor count. AST (20 mg/kg) suppressed the colonic inflammation as shown by decreased expression of NF-κB (1.8-fold) and NLRP3 (1.5-fold) against the control (1.0-fold). AST restored colon length and histopathological changes caused by AOM/DSS. AST inhibited the production of COX-2, INOS, and pro-inflammatory cytokines and chemokines, especially interleukin-6 (IL-6), IL-1β, and IL-10, by approximately 50% at 20 mg/kg. AST suppressed intestinal tissue ASC and IL-1β NLRP3 and NF-kB by approximately 1.3 times compared to control.

Conclusions: AST inhibited colorectal carcinoma growth by blocking the expression of NLRP3 and NF-κB and inducing an apoptotic cascade and suppressing iNOS-COX2 and IL-1β as regulators of inflammation and growth signal. This study advocates the application of phytopharmaceutical supplements for the management of colorectal carcinoma.

目的:炎症反应性NLRP3炎性小体和核因子κB (NF-κB)依赖的信号通路与炎症状况和疾病如结直肠癌(CRC)密切相关。可添加植物化学物质作为控制结直肠癌的预防性天然补充剂。在这项研究中,我们研究了在结直肠癌中,astl (AST)是否与抗炎NLRP3和NF-κ b依赖的分子事件相互作用。背景:生长信号氧化还原敏感转录因子NF-κB与NLRP3炎性体在结直肠癌进展中的相互作用网络需要有针对性的研究。AST是一种黄酮醇,据报道具有抗炎、免疫抑制和抗氧化特性,旨在通过NF-κB和NLRP3评估结直肠癌生长抑制作用。方法:应用AST对人源性HCT116和HT-29细胞进行细胞存活、凋亡、进展和DNA片段化检测,分析基因和蛋白表达及分子机制。结果:AST对HCT116和HT29的增殖均有抑制作用,其IC50值依赖于128和144事件。AST通过caspase-9和caspase-3激活的内在机制诱导结直肠癌细胞凋亡,导致G2/M期细胞周期阻滞。AST (100 μm)对两种细胞系的菌落形成能力和伤口愈合能力的抑制作用分别为54%和62%。在azoxymethane/dextran sodium sulfate (AOM/DSS)诱导的结肠炎相关结肠癌小鼠中,AST 20 mg/kg组总肿瘤数从14个减少到4.3个,显著降低了大肿瘤数。与对照组(1.0倍)相比,AST (20 mg/kg)对结肠炎症的抑制作用为NF-κB(1.8倍)和NLRP3(1.5倍)的表达降低。AST可恢复AOM/DSS引起的结肠长度和组织病理改变。在20 mg/kg剂量下,AST可抑制COX-2、INOS和促炎细胞因子和趋化因子的产生,尤其是白细胞介素-6 (IL-6)、IL-1β和IL-10的产生约50%。与对照组相比,AST抑制肠组织ASC和IL-1β NLRP3和NF-kB约为1.3倍。结论:AST通过阻断NLRP3和NF-κB的表达,诱导细胞凋亡级联,抑制iNOS-COX2和IL-1β作为炎症和生长信号的调节因子,抑制结直肠癌的生长。本研究提倡植物药物补充剂在大肠癌治疗中的应用。
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引用次数: 0
期刊
Indian Journal of Pharmacology
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