Science
Sea urchins made to order: Scripps scientists make transgenic breakthrough
Consider the sea urchin. Specifically, the painted urchin: Lytechinus pictus, a prickly Ping-Pong ball from the eastern Pacific Ocean.
The species is a smaller and shorter-spined cousin of the purple urchins devouring kelp forests. They produce massive numbers of sperm and eggs that fertilize outside of their bodies, allowing scientists to watch the process of urchin creation up close and at scale. One generation gives rise to the next in four to six months. They share more genetic material with humans than fruit flies do and can’t fly away — in short, an ideal lab animal for the developmental biologist.
Scientists have been using sea urchins to study cell development for roughly 150 years. Despite urchins’ status as super reproducers, practical concerns often compel scientists to focus their work on more easily accessible animals: mice, fruit flies, worms.
Scientists working with mice, for example, can order animals online with the specific genetic properties they are hoping to study — transgenic animals, whose genes have been artificially tinkered with to express or repress certain traits.
Researchers working with urchins typically have to spend part of their year collecting them from the ocean.
“Can you imagine if mouse researchers were setting a mousetrap every night, and whatever it is they caught is what they studied?” said Amro Hamdoun, a professor at UC San Diego’s Scripps Institution of Oceanography.
UC San Diego professor Amro Hamdoun holds a painted urchin. His breakthrough creating the creatures could lead to developments in science and medicine.
(Sandy Huffaker / For The Times)
Marine invertebrates represent about 40% of the animal world’s biological diversity yet appear in a scant fraction of a percentage of animal-based studies. What if researchers could access sea urchins as easily as mice? What if it were possible to make and raise lines of transgenic urchins?
How much more could we learn about how life works?
“You know how during the pandemic, everyone was making sourdough? I’m not good at making sourdough,” Hamdoun said recently at his office in Scripps’ Hubbs Hall. He set his sights instead on a project of a different sort: a new transgenic lab animal, “a fruit fly from the sea.”
In March, Hamdoun’s lab published a paper on the bioRxiv preprint server demonstrating the successful insertion of a piece of foreign DNA — specifically, a fluorescent protein from a jellyfish — into the genome of a painted urchin that passed the change down to its offspring.
The result is the first transgenic sea urchin, one that happens to glow like a Christmas bulb under a fluorescent light. (The paper has been submitted for peer review.)
The animals are the first transgenic echinoderms, the phylum that includes starfish, sea cucumbers and other marine animals. Hamdoun’s mission is to make genetically modified urchins available to researchers anywhere, not just those who happen to work in research facilities at the edge of the Pacific Ocean.
Postdoctoral researcher Elliot Jackson works with sea urchin eggs in a lab at Scripps.
(Sandy Huffaker / For The Times)
“If you look at some of the other model organisms, like Drosophila [fruit flies], zebrafish and mouse, there are well-established resource centers,” said Elliot Jackson, a postdoctoral researcher at Scripps and lead author of the paper. “If you want a transgenic line that labels the nervous system, you could probably get that. You could order it. And that’s what we hope we can be for sea urchins.”
Being able to genetically modify an animal supercharges what scientists can learn from it, with implications far beyond any individual species.
“It will transform sea urchins as a model for understanding neurobiology, for understanding developmental biology, for understanding toxicology,” said Christopher Lowe, a Stanford professor of biology who was not involved in the research.
The lab’s breakthrough, and its focus on making the animals freely available to fellow scientists, will “allow us to explore how evolution has solved a lot of really complicated life problems,” he said.
Researchers tend to study mice, flies and the like not because the animals’ biology is best suited to answer their questions but because “all the tools that were necessary to get at your questions were built up in just a few species,” said Deirdre Lyons, an associate professor of biology at Scripps who worked with Hamdoun on early research related to the project.
Expanding the range of animals available for sophisticated lab work is like adding colors to an artist’s palette, Lyons said: “Now you can go get the color that you really want, that best fits your vision, rather than being stuck with a few models.”
Painted urchins and humans live vastly different lives but genetically are quite similar.
(Sandy Huffaker / For The Times)
On the ground floor of Hamdoun’s office building is the Hubbs Hall experimental aquarium, a garage-like space crammed with tanks full of recirculating seawater and a motley assortment of marine life.
On a recent visit, Hamdoun reached into a tank and gently dislodged a painted urchin. It scooched with surprising speed across an outstretched palm, as if exploring alien terrain.
The last common ancestor of L. pictus and Homo sapiens lived at least 550 million years ago. Despite the different evolutionary paths we’ve since traveled, our genomes reveal a shared biological heritage.
The genetic instructions that drive the transformation of a single zygote into a living body are strikingly similar in our two species. Specialized systems differentiating from a single fertilized egg and the translation of a jumble of proteins into a singular living thing — on the cellular level, all of that proceeds in much the same way for urchins and people.
These animals are “really fundamental to our understanding of all of life,” Hamdoun said, placing the urchin back in its tank. “And historically, very inaccessible genetically.”
The experimental aquarium was built in the 1970s, when scooping life from the sea was the only way to acquire research specimens. A few floors up in Hubbs Hall, Hamdoun led the way into the urchin nursery — the first large-scale effort to raise successive generations of the animals in a laboratory. At any given moment, the team has 1,000 to 2,000 sea urchins in various stages of development.
Hamdoun points to transgenic sea urchins his lab is raising at Scripps.
(Sandy Huffaker / For The Times)
Row upon row of tiny plastic tanks stood against a wall, each containing a lentil-size juvenile urchin. A strip of tape on each tank noted the animal’s genetic modification and date of fertilization. On some, a second bit of tape indicated animals that had the modification in their sex cells’ DNA, meaning it could be passed down to offspring. (For this reason, the lab keeps its urchins scrupulously separate from the wild population.)
“One of the big questions in all of biology is to understand how the series of instructions in the genome gives you whatever phenotype you want to study,” Hamdoun said — essentially, how the string of amino acids that is an animal’s genetic code gives rise to the characteristics of the living, respiring creature. “One of the fundamental things you have to do is be able to modify that genome, and then study what the outcome is.”
He pointed to a tank containing a tiny urchin from whose genetic code the protein ABCD1 has been snipped.
ABCD1 acts like a bouncer, Hamdoun explained, parking along the cell membrane and ejecting foreign molecules. The protein’s action can preserve the cell from harmful substances but can sometimes work against an organism’s best interest, as when it prevents the cell from absorbing a necessary medication.
Researchers using urchins in which that protein no longer works can study the movement of a molecule through an organism — DDT, for example — and measure how much of the substance ends up in the cell without the confounding interference of ABCD1. They can reverse-engineer how big a role ABCD1 plays in preventing a cell from absorbing a drug.
One biology professor said Scripps’ work will transform sea urchins as a model for research.
(Sandy Huffaker / For The Times)
And then there are the fluorescent urchins.
“The magic happens in this room,” Jackson said, walking into a narrow office with $1 million worth of microscopes at one end and a decades-old hand-cranked centrifuge bolted to a table at another.
He placed a petri dish containing three pencil-eraser-size transgenic urchins under a microscope. At 120 times its size, each looked like the Times Square New Year’s Eve ball come to life — a glowing, wiggling creature of pentamerous radial symmetry.
Fluorescence is not just an echinoderm party trick. Lighting up the cells makes it easier for researchers to track their movement in a developing organism. Researchers can watch as the early cells of a blastula divide and reorganize into neural or cardiac tissue. Eventually, scientists will be able to turn off individual genes and see how that affects development. It will help us understand how our own species develops, and why that development doesn’t always proceed according to plan.
The lab has “done a great job. It’s really been welcomed by the community,” said Marko Horb, senior scientist and director of the National Xenopus Resource at the University of Chicago’s Marine Biological Laboratory.
Horb runs the national clearinghouse for genetically modified species of Xenopus, a clawed frog used in lab research. Funded in part by the National Institutes of Health, the center develops lines of transgenic frogs for scientific use and distributes them to researchers.
Hamdoun envisions a similar resource center for his lab’s urchins. They’ve already started sending tiny vials of transgenic urchin sperm to interested scientists, who can grow bespoke urchins with eggs acquired from Hamdoun’s lab or another source.
Hamdoun vividly recalls the time he spent earlier in his career trying to track down random snippets of DNA necessary for his research, the disappointment and frustration of writing to professors and former postdocs only to find that the material had long been lost. He’d rather future generations of scientists spend their time on discovery.
“Biology is really interesting,” he said. “The more people can get access to it, the more we’re going to learn.”
Three transgenic sea urchins in a petri dish.
(Sandy Huffaker / For The Times)
Science
California’s last nuclear plant clears major hurdle to power on
California environmental regulators on Thursday struck a landmark deal with Pacific Gas & Electric to extend the life of the state’s last remaining nuclear power plant in exchange for thousands of acres of new land conservation in San Luis Obispo County.
PG&E’s agreement with the California Coastal Commission is a key hurdle for the Diablo Canyon nuclear plant to remain online until at least 2030. The plant was slated to close this year, largely due to concerns over seismic safety, but state officials pushed to delay it — saying the plant remains essential for the reliable operation of California’s electrical grid. Diablo Canyon provides nearly 9% of the electricity generated in the state, making it the state’s single largest source.
The Coastal Commission voted 9-3 to approve the plan, settling the fate of some 12,000 acres that surround the power plant as a means of compensation for environmental harm caused by its continued operation.
Nuclear power does not emit greenhouse gases. But Diablo Canyon uses an estimated 2.5 billion gallons of ocean water each day to absorb heat in a process known as “once-through cooling,” which kills an estimated two billion or more marine organisms each year.
Some stakeholders in the region celebrated the conservation deal, while others were disappointed by the decision to trade land for marine impacts — including a Native tribe that had hoped the land would be returned to them. Diablo Canyon sits along one of the most rugged and ecologically rich stretches of the California coast.
Under the agreement, PG&E will immediately transfer a 4,500-acre parcel on the north side of the property known as the “North Ranch” into a conservation easement and pursue transfer of its ownership to a public agency such as the California Department of Parks and Recreation, a nonprofit land conservation organization or tribe. A purchase by State Parks would result in a more than 50% expansion of the existing Montaña de Oro State Park.
PG&E will also offer a 2,200-acre parcel on the southern part of the property known as “Wild Cherry Canyon” for purchase by a government agency, nonprofit land conservation organization or tribe. In addition, the utility will provide $10 million to plan and manage roughly 25 miles of new public access trails across the entire property.
“It’s going to be something that changes lives on the Central Coast in perpetuity,” Commissioner Christopher Lopez said at the meeting. “This matters to generations that have yet to exist on this planet … this is going to be a place that so many people mark in their minds as a place that transforms their lives as they visit and recreate and love it in a way most of us can’t even imagine today.”
Critically, the plan could see Diablo Canyon remain operational much longer than the five years dictated by Thursday’s agreement. While the state Legislature only authorized the plant to operate through 2030, PG&E’s federal license renewal would cover 20 years of operations, potentially keeping it online until 2045.
Should that happen, the utility would need to make additional land concessions, including expanding an existing conservation area on the southern part of the property known as the “South Ranch” to 2,500 acres. The plan also includes rights of first refusal for a government agency or a land conservation group to purchase the entirety of the South Ranch, 5,000 acres, along with Wild Cherry Canyon — after 2030.
Pelicans along the concrete breakwater at Pacific Gas and Electric’s Diablo Canyon Power Plant
(Brian van der Brug/Los Angeles Times)
Many stakeholders were frustrated by the carve-out for the South Ranch, but still saw the agreement as an overall victory for Californians.
“It is a once in a lifetime opportunity,” Sen. John Laird (D-Santa Cruz) said in a phone call ahead of Thursday’s vote. “I have not been out there where it has not been breathtakingly beautiful, where it is not this incredible, unique location, where you’re not seeing, for much of it, a human structure anywhere. It is just one of those last unique opportunities to protect very special land near the California coast.”
Others, however, described the deal as disappointing and inadequate.
That includes many of the region’s Native Americans who said they felt sidelined by the agreement. The deal does not preclude tribal groups from purchasing the land in the future, but it doesn’t guarantee that or give them priority.
The yak titʸu titʸu yak tiłhini Northern Chumash Tribe of San Luis Obispo County and Region, which met with the Coastal Commission several times in the lead-up to Thursday’s vote, had hoped to see the land returned to them.
Scott Lanthrop is a member of the tribe’s board and has worked on the issue for several years.
“The sad part is our group is not being recognized as the ultimate conservationist,” he told The Times. “Any normal person, if you ask the question, would you rather have a tribal group that is totally connected to earth and wind and water, or would you like to have some state agency or gigantic NGO manage this land, I think the answer would be, ‘Hey, you probably should give it back to the tribe.’”
Tribe chair Mona Tucker said she fears that free public access to the land could end up harming it instead of helping it, as the Coastal Commission intends.
“In my mind, I’m not understanding how taking the land … is mitigation for marine life,” Tucker said. “It doesn’t change anything as far as impacts to the water. It changes a lot as far as impacts to the land.”
Montaña de Oro State Park.
(Christopher Reynolds / Los Angeles Times)
The deal has been complicated by jurisdictional questions, including who can determine what happens to the land. While PG&E owns the North Ranch parcel that could be transferred to State Parks, the South Ranch and Wild Cherry Canyon are owned by its subsidiary, Eureka Energy Company.
What’s more, the California Public Utilities Commission, which regulates utilities such as PG&E, has a Tribal Land Transfer Policy that calls for investor-owned power companies to transfer land they no longer want to Native American tribes.
In the case of Diablo Canyon, the Coastal Commission became the decision maker because it has the job of compensating for environmental harm from the facility’s continued operation. Since the commission determined Diablo’s use of ocean water can’t be avoided, it looked at land conservation as the next best method.
This “out-of-kind” trade-off is a rare, but not unheard of way of making up for the loss of marine life. It’s an approach that is “feasible and more likely to succeed” than several other methods considered, according to the commission’s staff report.
“This plan supports the continued operation of a major source of reliable electricity for California, and is in alignment with our state’s clean energy goals and focus on coastal protection,” Paula Gerfen, Diablo Canyon’s senior vice president and chief nuclear officer, said in a statement.
But Assemblymember Dawn Addis (D-Morro Bay) said the deal was “not the best we can do” — particularly because the fate of the South Ranch now depends on the plant staying in operation beyond 2030.
“I believe the time really is now for the immediate full conservation of the 12,000 [acres], and to bring accountability and trust back for the voters of San Luis Obispo County,” Addis said during the meeting.
There are also concerns about the safety of continuing to operate a nuclear plant in California, with its radioactive waste stored in concrete casks on the site. Diablo Canyon is subject to ground shaking and earthquake hazards, including from the nearby Hosgri Fault and the Shorline Fault, about 2.5 miles and 1 mile from the facility, respectively.
PG&E says the plant has been built to withstand hazards. It completed a seismic hazard assessment in 2024, and determined Diablo Canyon is safe to continue operation through 2030. The Coastal Commission, however, found if the plant operates longer, it would warrant further seismic study.
A key development for continuing Diablo Canyon’s operation came in 2022 with Senate Bill 846, which delayed closure by up to five additional years. At the time, California was plagued by rolling blackouts driven extreme heat waves, and state officials were growing wary about taking such a major source of power offline.
But California has made great gains in the last several years — including massive investments in solar energy and battery storage — and some questioned whether the facility is still needed at all.
Others said conserving thousands of acres of land still won’t make up for the harms to the ocean.
“It is unmitigatable,” said David Weisman, executive director of the nonprofit Alliance for Nuclear Responsibility. He noted that the Coastal Commission’s staff report says it would take about 99 years to balance the loss of marine life with the benefits provided by 4,500 acres of land conservation. Twenty more years of operation would take about 305 years to strike that same balance.
But some pointed out that neither the commission nor fisheries data find Diablo’s operations cause declines in marine life. Ocean harm may be overestimated, said Seaver Wang, an oceanographer and the climate and energy director at the Breakthrough Institute, a Berkeley-based research center.
In California’s push to transition to clean energy, every option comes with downsides, Wang said. In the case of nuclear power — which produces no greenhouse gas emissions — it’s all part of the trade off, he said.
“There’s no such thing as impacts-free energy,” he said.
The Coastal Commission’s vote is one of the last remaining obstacles to keeping the plant online. PG&E will also need a final nod from the Regional Water Quality Control Board, which decides on a pollution discharge permit in February.
The federal Nuclear Regulatory Commission will also have to sign off on Diablo’s extension.
Science
In search for autism’s causes, look at genes, not vaccines, researchers say
Earlier this year, Health and Human Services Secretary Robert F. Kennedy Jr. pledged that the search for autism’s cause — a question that has kept researchers busy for the better part of six decades — would be over in just five months.
“By September, we will know what has caused the autism epidemic, and we’ll be able to eliminate those exposures,” Kennedy told President Trump during a Cabinet meeting in April.
That ambitious deadline has come and gone. But researchers and advocates say that Kennedy’s continued fixation on autism’s origins — and his frequent, inaccurate claims that childhood vaccines are somehow involved — is built on fundamental misunderstandings of the complex neurodevelopmental condition.
Even after more than half a century of research, no one yet knows exactly why some people have autistic traits and others do not, or why autism spectrum disorder looks so different across the people who have it. But a few key themes have emerged.
Researchers believe that autism is most likely the result of a complex set of interactions between genes and the environment that unfold while a child is in the womb. It can be passed down through families, or originate with a spontaneous gene mutation.
Environmental influences may indeed play a role in some autism cases, but their effect is heavily influenced by a person’s genes. There is no evidence for a single trigger that causes autism, and certainly not one a child encounters after birth: not a vaccine, a parenting style or a post-circumcision Tylenol.
“The real reason why it’s complicated, the more fundamental one, is that there’s not a single cause,” said Irva Hertz-Picciotto, a professor of public health science and director of the Environmental Health Sciences Center at UC Davis. “It’s not a single cause from one person to the next, and not a single cause within any one person.”
Kennedy, an attorney who has no medical or scientific training, has called research into autism’s genetics a “dead end.” Autism researchers counter that it’s the only logical place to start.
“If we know nothing else, we know that autism is primarily genetic,” said Joe Buxbaum, a molecular neuroscientist who directs the Seaver Autism Center for Research and Treatment at the Icahn School of Medicine at Mount Sinai. “And you don’t have to actually have the exact genes [identified] to know that something is genetic.”
Some neurodevelopment disorders arise from a difference in a single gene or chromosome. People with Down syndrome have an extra copy of chromosome 21, for example, and Fragile X syndrome results when the FMR1 gene isn’t expressed.
Autism in most cases is polygenetic, which means that multiple genes are involved, with each contributing a little bit to the overall picture.
Researchers have found hundreds of genes that could be associated with autism; there may be many more among the roughly 20,000 in the human genome.
In the meantime, the strongest evidence that autism is genetic comes from studies of twins and other sibling groups, Buxbaum and other researchers said.
The rate of autism in the U.S. general population is about 2.8%, according to a study published last year in the journal Pediatrics. Among children with at least one autistic sibling, it’s 20.2% — about seven times higher than the general population, the study found.
Twin studies reinforce the point. Both identical and fraternal twins develop in the same womb and are usually raised in similar circumstances in the same household. The difference is genetic: identical twins share 100% of their genetic information, while fraternal twins share about 50% (the same as nontwin siblings).
If one fraternal twin is autistic, the chance that the other twin is also autistic is about 20%, or about the same as it would be for a nontwin sibling.
But if one in a pair of identical twins is autistic, the chance that the other twin is also autistic is significantly higher. Studies have pegged the identical twin concurrence rate anywhere from 60% to 90%, though the intensity of the twins’ autistic traits may differ significantly.
Molecular genetic studies, which look at the genetic information shared between siblings and other blood relatives, have found similar rates of genetic influence on autism, said Dr. John Constantino, a professor of pediatrics, psychiatry and behavioral sciences at the Emory University School of Medicine and chief of behavioral and mental health at Children’s Healthcare of Atlanta.
Together, he said, “those studies have indicated that a vast share of the causation of autism can be traced to the effects of genetic influences. That is a fact.”
Buxbaum compares the heritability of autism to the heritability of height, another polygenic trait.
“There’s not one gene that’s making you taller or shorter,” Buxbaum said. Hundreds of genes play a role in where you land on the height distribution curve. A lot of those genes run in families — it’s not unusual for very tall people, for example, to have very tall relatives.
But parents pass on a random mix of their genes to their children, and height distribution across a group of same-sex siblings can vary widely. Genetic mutations can change the picture. Marfan syndrome, a condition caused by mutations in the FBN1 gene, typically makes people grow taller than average. Hundreds of genetic mutations are associated with dwarfism, which causes shorter stature.
Then once a child is born, external factors such as malnutrition or disease can affect the likelihood that they reach their full height potential.
So genes are important. But the environment — which in developmental science means pretty much anything that isn’t genetics, including parental age, nutrition, air pollution and viruses — can play a major role in how those genes are expressed.
“Genetics does not operate in a vacuum, and at the same time, the impact of the environment on people is going to depend on a person’s individual genetics,” said Brian K. Lee, a professor of epidemiology and biostatistics at Drexel University who studies the genetics of developmental disorders.
Unlike the childhood circumstances that can affect height, the environmental exposures associated with autism for the most part take place in utero.
Researchers have identified multiple factors linked to increased risks of the disorder, including older parental age, infant prematurity and parental exposure to air pollution and industrial solvents.
Investigations into some of these linkages were among the more than 50 autism-related studies whose funding Kennedy has cut since taking office, a ProPublica investigation found. In contrast, no credible study has found links between vaccines and autism — and there have been many.
One move from the Department of Health and Human Services has been met with cautious optimism: even as Kennedy slashed funding to other research projects, the department in September announced a $50-million initiative to explore the interactions of genes and environmental factors in autism, which has been divided among 13 different research groups at U.S. universities, including UCLA and UC San Diego.
The department’s selection of well-established, legitimate research teams was met with relief by many autism scientists.
But many say they fear that such decisions will be an anomaly under Kennedy, who has repeatedly rejected facts that don’t conform to his preferred hypotheses, elevated shoddy science and muddied public health messaging on autism with inaccurate information.
Disagreements are an essential part of scientific inquiry. But the productive ones take place in a universe of shared facts and build on established evidence.
And when determining how to spend limited resources, researchers say, making evidence-based decisions is vital.
“There are two aspects of these decisions: Is it a reasonable expenditure based on what we already know? And if you spend money here, will you be taking money away from HHS that people are in desperate need of?” Constantino said. “If you’re going to be spending money, you want to do that in a way that is not discarding what we already know.”
Science
Contributor: New mothers are tempted by Ozempic but don’t have the data they need
My friend Sara, eight weeks after giving birth, left me a tearful voicemail. I’m a clinical psychologist specializing in postpartum depression and psychosis, but mental health wasn’t Sara’s issue. Postpartum weight gain was.
Sara told me she needed help. She’d gained 40 pounds during her pregnancy, and she was still 25 pounds overweight. “I’m going back to work and I can’t look like this,” she said. “I need to take Ozempic or something. But do you know if it’s safe?”
Great question. Unfortunately researchers don’t yet have an answer. On Dec. 1, the World Health Organization released its first guidelines on the use of GLP-1 receptor agonists such as Ozempic, generically known as semaglutide. One of the notable policy suggestions in that report is to not prescribe GLP-1s to pregnant women. Disappointingly, the report says nothing about the use of the drug by postpartum women, including those who are breastfeeding.
There was a recent Danish study that led to medical guidelines against prescribing to patients who are pregnant or breastfeeding.
None of that is what my friend wanted to hear. I could only encourage her to speak to her own medical doctor.
Sara’s not alone. I’ve seen a trend emerging in my practice in which women use GLP-1s to shed postpartum weight. The warp speed “bounce-back” ideal of body shapes for new mothers has reemerged, despite the mental health field’s advocacy to abolish the archaic pressure of martyrdom in motherhood. GLP-1s are being sold and distributed by compound pharmacies like candy. And judging by their popularity, nothing tastes sweeter than skinny feels.
New motherhood can be a stressful time for bodies and minds, but nature has also set us up for incredible growth at that moment. Contrary to the myth of spaced-out “mommy brains,” new neuroplasticity research shows that maternal brains are rewired for immense creativity and problem solving.
How could GLP-1s affect that dynamic? We just don’t know. We do know that these drugs are associated with changes far beyond weight loss, potentially including psychiatric effects such as combating addiction.
Aside from physical effects, this points to an important unanswered research question: What effects, if any, do GLP-1s have on a woman’s brain as it is rewiring to attune to and take care of a newborn? And on a breastfeeding infant? If GLP-1s work on the pleasure center of the brain and your brain is rewiring to feel immense pleasure from a baby coo, I can’t help but wonder if that will be dampened. When a new mom wants a prescription for a GLP-1 to help shed baby weight, her medical provider should emphasize those unknowns.
These drugs may someday be a useful tool for new mothers. GLP-1s are helping many people with conditions other than obesity. A colleague of mine was born with high blood pressure and cholesterol. She exercised every day and adopted a pescatarian diet. Nothing budged until she added a GLP-1 to her regimen, bringing her blood pressure to a healthy 120/80 and getting cholesterol under control. My brother, an otherwise healthy young man recently diagnosed with a rare idiopathic lymphedema of his left leg, is considering GLP-1s to address inflammation and could be given another chance at improving his quality of life.
I hope that GLP-1s will continue to help those who need it. And I urge everyone — especially new moms — to proceed with caution. A healthy appetite for nutritious food is natural. That food fuels us for walks with our dogs, swims along a coastline, climbs through leafy woods. It models health and balance for the young ones who are watching us for clues about how to live a healthy life.
Nicole Amoyal Pensak, a clinical psychologist and researcher, is the author of “Rattled: How to Calm New Mom Anxiety With the Power of the Postpartum Brain.”
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