
Indian Snake Species Can Still Inject Venom Hours After Death, New Study Reveals
The research team, led by Susmita Thakur from Namrup College in Assam, documented three incidents involving venomous snakes. Two cases involved monocled cobras (Naja kaouthia) and one involved a black krait (Bungarus lividus), all reported to rural health centres in Assam.
First Incident
In the first instance, a 45-year-old man killed a snake that was attacking chickens in his home by beheading it. When the man tried to dispose of the snake's body, the severed head bit him on the thumb. He immediately felt severe pain radiating from the bite site to his shoulder. At the hospital, he reported symptoms including repeated vomiting, unbearable pain, and the bite area began to blacken. A photo of the snake helped doctors confirm it was a monocled cobra bite.
The man received intravenous antivenom and pain relief medication at the hospital and was discharged after 20 days with follow-up care for wound management.
"The pain significantly decreased following this treatment. The patient did not develop any symptoms of neurotoxicity," the researchers noted.
Second Incident
In a separate incident, a man working in a paddy field accidentally ran over a monocled cobra with his tractor. However, when he stepped off, the supposedly dead snake bit him on the foot. The patient experienced severe pain, swelling, and discolouration at the bite site, as well as two episodes of vomiting in the hospital, indicating envenomation. Although there were no signs of neurotoxicity, the bite caused an ulcer.
"Despite being crushed and presumed to be dead for several hours, the snake was capable of delivering a venomous bite, requiring antivenom treatment along with extended wound care," the researchers wrote.
Third Incident
In the third incident, a black snake entered a house and was killed, with its body discarded in the backyard. A neighbour who later picked up the snake's head was bitten on the finger. Within hours, the neighbour experienced difficulty swallowing and drooping eyelids.
Doctors identified the snake as a black krait (Bungarus lividus) and confirmed that the bite occurred despite the snake having been dead for 3 hours. The patient's condition worsened despite receiving 20 vials of polyvalent antivenom, and he became quadriplegic and unresponsive. After 43 hours of respiratory support, his condition improved, and he was discharged from the hospital in good health after six days.
Why does it happen?
Based on these incidents, researchers cautioned that snakes can still deliver venom even after fatal injuries, posing a risk of severe complications.
The researchers found that certain snakes' venom apparatus allows them to deliver venom even after death due to its unique structure. The venom gland, connected to a hollow fang, can still release venom if accidentally pressed while handling the severed head. This can lead to severe symptoms similar to those caused by live snake bites.
Hashtags

Try Our AI Features
Explore what Daily8 AI can do for you:
Comments
No comments yet...
Related Articles
&w=3840&q=100)

Business Standard
11 minutes ago
- Business Standard
Japan's Takeda weighs India for global trials to speed up drug launches
Takeda is also open to partnering with local academia, healthcare providers and technology firms in India for innovation, Das said, without sharing more specifics The plan comes at a time when India's clinical trials market is growing, powered by diverse patient pools, cost efficiency, and a fast-growing hospital network Reuters Japanese drugmaker Takeda Pharmaceutical is exploring the option of conducting global clinical trials in India to accelerate the launch of its innovative drugs in the world's most populous nation, its India head told Reuters. The plan comes at a time when India's clinical trials market is growing, powered by diverse patient pools, cost efficiency, and a fast-growing hospital network. Grand View Research expects the market to exceed $2 billion by 2030. "India is a strategic growth market for Takeda, and we are making significant long-term investments... in terms of innovation and building capabilities," said Annapurna Das, the general manager of Takeda's India operations. She did not share financial details of the investments. "We're exploring the opportunity of leveraging India's clinical trial ecosystem," Das said. Takeda is also open to partnering with local academia, healthcare providers and technology firms in India for innovation, Das said, without sharing more specifics. "At this point of time, we are still kind of exploring and evaluating how we want to go ahead," she added. Takeda's eventual aim is to integrate India's research and development "ecosystem" into its global pipeline and expand Indian patients' access to cutting-edge therapies in oncology, neuroscience, gastrointestinal health, and inflammation. The Japanese drugmaker aims to launch key cancer drugs over the next two to three years in India, with a lung cancer drug ready to hit the market this year. There's also a dengue vaccine in its launch pipeline, for which Takeda has tied up with local vaccine maker Biological E., and is awaiting approval from India's drug regulator. Takeda established an innovation centre in Bengaluru, dubbed India's "Silicon Valley", earlier this year to tap the country's tech talent to power its global digital transformation. The centre is expanding to have 750 staff working in AI, data science, engineering, and design, from just over 500 employees currently. (Only the headline and picture of this report may have been reworked by the Business Standard staff; the rest of the content is auto-generated from a syndicated feed.)


Hindustan Times
an hour ago
- Hindustan Times
Japan's Takeda weighs India for global trials to speed up drug launches
By Rishika Sadam and Bhanvi Satija Japan's Takeda weighs India for global trials to speed up drug launches -Japanese drugmaker Takeda Pharmaceutical is exploring the option of conducting global clinical trials in India to accelerate the launch of its innovative drugs in the world's most populous nation, its India head told Reuters. The plan comes at a time when India's clinical trials market is growing, powered by diverse patient pools, cost efficiency, and a fast-growing hospital network. Grand View Research expects the market to exceed $2 billion by 2030. "India is a strategic growth market for Takeda, and we are making significant long-term investments... in terms of innovation and building capabilities," said Annapurna Das, the general manager of Takeda's India operations. She did not share financial details of the investments. "We're exploring the opportunity of leveraging India's clinical trial ecosystem," Das said. Takeda is also open to partnering with local academia, healthcare providers and technology firms in India for innovation, Das said, without sharing more specifics. "At this point of time, we are still kind of exploring and evaluating how we want to go ahead," she added. Takeda's eventual aim is to integrate India's research and development "ecosystem" into its global pipeline and expand Indian patients' access to cutting-edge therapies in oncology, neuroscience, gastrointestinal health, and inflammation. The Japanese drugmaker aims to launch key cancer drugs over the next two to three years in India, with a lung cancer drug ready to hit the market this year. There's also a dengue vaccine in its launch pipeline, for which Takeda has tied up with local vaccine maker Biological E., and is awaiting approval from India's drug regulator. Takeda established an innovation centre in Bengaluru, dubbed India's "Silicon Valley", earlier this year to tap the country's tech talent to power its global digital transformation. The centre is expanding to have 750 staff working in AI, data science, engineering, and design, from just over 500 employees currently. This article was generated from an automated news agency feed without modifications to text.


NDTV
2 hours ago
- NDTV
Early Puberty, Childbirth Linked To Faster Ageing, High Diabetes Risk: Study
When puberty begins very early or a first baby arrives in the late teens, it can feel like life is simply running ahead of schedule. New research suggests the body may be doing the same when women go through these life and health landmarks early: ageing faster under the hood. A recently published study in eLife reports that early menarche (first period) and childbirth before 21 are associated with accelerated biological ageing and sharply higher risks of age-related diseases. Conversely, later puberty and later first birth were linked with slower epigenetic ageing, lower frailty, and reduced risk of conditions like type 2 diabetes and Alzheimer's disease. The findings, based on large-scale genetic and cohort analyses, build on a growing body of evidence that reproductive milestones can influence lifelong metabolic and cardiovascular health. For Indian readers, especially women, this matters. India now has an estimated 101 million people living with diabetes and 136 million with prediabetes, many of them women balancing work, family and caregiving. Understanding how reproductive timing intersects with long-term risk can help women and clinicians plan screening, prevention and support without stigma or blame. What Did The New Study Find? Researchers analysed data from hundreds of thousands of participants and used genetic approaches to reduce confounding, concluding that early menarche (before approximately 11 years) and early childbirth (before 21 years) are linked to faster biological or "epigenetic" ageing and substantially higher odds of several age-related diseases. In the UK Biobank subset, the authors report that early menarche and early first birth almost doubled the risk of type 2 diabetes and heart failure and quadrupled the risk of obesity; later timing showed the opposite pattern of slower ageing and lower disease risk. These results are consistent with an "antagonistic pleiotropy" idea: traits that support early reproduction may carry long-term health costs. Independent, recent evidence supports the link between reproductive events and ageing biology. For example, a 2024 study published in PNAS found pregnancy was associated with "older" biological signatures on certain epigenetic measures, while broader research connects epigenetic age acceleration with chronic disease and functional decline. Together, these strands point to a real, measurable interface between reproductive history and later-life health. Why This Matters For Women's Health In India India is grappling with a high and rising metabolic disease burden. The ICMR-INDIAB analysis estimated 101 million with diabetes and 136 million with prediabetes in 2023-figures with clear implications for screening and prevention among women across the life course. If early puberty and early childbirth amplify future metabolic and cardiac risk, earlier and more proactive monitoring becomes essential. There are also population trends to consider. Nationally representative analyses, especially one published in Scientific Reports in 2024, show the mean age at menarche in India is about 13.5 years, with a gradual secular decline across birth cohorts-meaning some girls are entering puberty earlier than previous generations. While early menarche is not destiny, its association with later risk highlights the importance of adolescent nutrition, physical activity, psychosocial support and timely sexual-reproductive health counselling. For young women who become mothers in their teens, even late teens, the new findings argue for stronger postpartum follow-up, diabetes and lipid screening, and support to maintain heart-healthy behaviours while juggling childcare, work and study. How Could Early Reproductive Timing Influence Disease Risk? Scientists increasingly look at epigenetic ageing clocks, the chemical tags on DNA that track biological wear-and-tear. Stressors such as rapid developmental change, pregnancy, under-nutrition or psychosocial adversity may accelerate these clocks in some contexts. Early reproductive events might therefore "pull forward" biological ageing, interacting with well-known drivers like diet quality, physical inactivity, sleep debt, tobacco exposure and air pollution. The result is a higher lifetime probability of metabolic and cardiovascular disease-particularly without regular screening and risk-factor control. Help young girls and women understand their medical history and why it matters Photo Credit: Pexels What Every Woman Should Note: Practical Takeaways Whenever a new study comes out claiming findings that may have long-term impact on public health, it is natural for readers to get alarmed. However, it is very important that Indian women take note of this study and take the following practical takeaways: This is risk, not fate Early periods or a first baby in the teens does not doom anyone to diabetes or heart disease. It signals a need for closer prevention and screening methods which work. Lifestyle changes and evidence-based care can substantially reduce risk. Know your numbers-regularly If you had early menarche or gave birth before 21, ask your clinician about earlier and periodic screening: fasting glucose or HbA1c, blood pressure, lipids, BMI/waist, and (if pregnant now or planning) screening for gestational diabetes. Given India's burden, routine checks from your mid-20s onward are reasonable, or sooner if you have weight gain, strong family history or symptoms. Prioritise cardio-metabolic habits Aim for 150-300 minutes/week of moderate activity plus muscle-strengthening twice weekly; build vegetable-rich, fibre-forward plates with adequate protein; limit ultra-processed foods and added sugars; sleep 7-9 hours; avoid or stop smoking; and reduce second-hand smoke exposure. These steps delay biological ageing patterns and cut diabetes/CVD risk. Pregnancy planning and postpartum care matter If you had a teen pregnancy or gestational diabetes, discuss postpartum glucose testing and long-term follow-up. Evidence shows pregnancy can shift epigenetic ageing markers; checking in after delivery protects future health. Support adolescents For parents and educators, provide balanced nutrition, physical activity, iron sufficiency, mental-health support, and age-appropriate reproductive education. Earlier menarche trends make these investments even more important. There are also some important caveats everyone should note: Association vs causation: The eLife paper used genetic and observational methods to strengthen causal inference, yet unmeasured factors can remain. Findings should guide screening and prevention, not stigma. Population differences: Much evidence comes from cohorts such as UK Biobank; translation to all Indian sub-populations requires local studies. Still, given India's diabetes prevalence, a prudent, preventive approach is justified. Biology is modifiable: Epigenetic ageing markers are not fixed. Lifestyle change, appropriate therapy for blood sugar and blood pressure, and mental-health support can improve long-term outcomes. The new analysis adds a compelling chapter to women's health: earlier puberty and early childbirth appear to accelerate biological ageing and raise risks for diabetes, heart failure and obesity, while later timing generally protects. For Indian women, the message is empowering, not alarming. Know your reproductive history, screen earlier if you're higher-risk, and double down on everyday prevention. Those steps, sustained over years, are powerful tools to bend the risk curve in your favour.