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	<title>creatine &#8211; Science</title>
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	<title>creatine &#8211; Science</title>
	<link>https://scienmag.com</link>
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		<title>Puberty-Blocking Drug Reshapes Cortical Growth and Brain Metabolism in Animal Study</title>
		<link>https://scienmag.com/puberty-blocking-drug-reshapes-cortical-growth-and-brain-metabolism-in-animal-study/</link>
		
		<dc:creator><![CDATA[Cassandra Pierce]]></dc:creator>
		<pubDate>Sat, 10 Oct 2026 02:25:59 +0000</pubDate>
				<category><![CDATA[Psychology & Psychiatry]]></category>
		<category><![CDATA[adolescent neurodevelopment]]></category>
		<category><![CDATA[animal models for puberty and brain development]]></category>
		<category><![CDATA[brain metabolism]]></category>
		<category><![CDATA[cortical development]]></category>
		<category><![CDATA[cortical growth and metabolism during puberty suppression]]></category>
		<category><![CDATA[creatine]]></category>
		<category><![CDATA[diffusion imaging]]></category>
		<category><![CDATA[gender dysphoria]]></category>
		<category><![CDATA[gender dysphoria treatment and brain effects]]></category>
		<category><![CDATA[glutamate]]></category>
		<category><![CDATA[GnRHa]]></category>
		<category><![CDATA[GnRHa effects on adolescent brain development]]></category>
		<category><![CDATA[long-term effects of pubertal hormone suppression]]></category>
		<category><![CDATA[longitudinal animal study on puberty suppression]]></category>
		<category><![CDATA[magnetic resonance imaging]]></category>
		<category><![CDATA[MR spectroscopy]]></category>
		<category><![CDATA[multimodal brain imaging in puberty research]]></category>
		<category><![CDATA[neural impact of hormonal suppression in adolescents]]></category>
		<category><![CDATA[neurobiological consequences of puberty delay]]></category>
		<category><![CDATA[nuclear magnetic resonance spectroscopy in brain research]]></category>
		<category><![CDATA[puberty blockers]]></category>
		<category><![CDATA[puberty-blocking drugs]]></category>
		<category><![CDATA[structural and diffusion MRI in puberty studies]]></category>
		<category><![CDATA[triptorelin]]></category>
		<guid isPermaLink="false">https://scienmag.com/?p=257026</guid>

					<description><![CDATA[A longitudinal animal study finds that the puberty-blocking drug triptorelin attenuates neocortical growth, alters tissue microstructure, and shifts brain metabolite levels, offering a translational framework for interpreting neuroimaging in adolescents treated with GnRHa.]]></description>
										<content:encoded><![CDATA[<p>One of the most contested questions in modern medicine is what happens to the adolescent brain when puberty is chemically paused. Gonadotropin-releasing hormone agonists, or GnRHa, are widely prescribed to suppress the hormonal surge of puberty in adolescents with gender dysphoria, yet the neurobiological consequences of this intervention have remained largely unresolved. A new longitudinal study published in Translational Psychiatry now offers the most detailed multimodal picture to date of how pubertal endocrine suppression alters cortical development, using an animal model tracked with structural magnetic resonance imaging, diffusion imaging, and high-resolution nuclear magnetic resonance spectroscopy.</p>
<p>The research team, led by Alberto Marcos and Antonio Guillamon of the Universidad Nacional de Educación a Distancia in Madrid, together with colleagues at the Institute for Biomedical Research Sols-Morreale, the University of A Coruña, the University of Deusto, and the Biomedical Research Networking Centre on Rare Diseases, designed a translational experiment to isolate the effects of pubertal hormones on the developing brain. Animals received long-acting triptorelin, a GnRHa, beginning at the onset of puberty, and were then followed over time with repeated in vivo brain imaging. The design is significant because it is longitudinal: rather than comparing snapshots of different individuals, the researchers watched the same brains change, or fail to change, across the pubertal window.</p>
<p>Triptorelin works by flooding the pituitary&#8217;s GnRH receptors, which paradoxically desensitizes the hypothalamic-pituitary-gonadal axis and shuts down the release of luteinizing hormone and follicle-stimulating hormone. The result, confirmed in this study, is that testosterone was held at prepubertal levels throughout the treatment period. This pharmacological clamp allowed the investigators to ask a deceptively simple question: if the hormonal signal of puberty is removed, does the brain still follow its usual developmental script?</p>
<p>The structural imaging data delivered a clear answer: it does not, at least not entirely. Animals treated with triptorelin showed attenuated growth of bilateral neocortical volume, meaning the cortex, the brain&#8217;s wrinkled outer sheet responsible for sensory processing, executive control, and complex cognition, expanded less than expected during the pubertal period. Crucially, this effect was regionally specific rather than global. Total brain volume remained unchanged, indicating that the drug did not simply stunt overall brain growth or cause generalized tissue loss. Instead, the hormonal suppression selectively blunted the developmental expansion of the neocortex, the very structure that undergoes some of its most dramatic maturational change during adolescence.</p>
<p>This dissociation between total brain volume and cortical volume is scientifically important. Puberty is known to be a period of profound cortical reorganization, including ongoing myelination, synaptic pruning, and changes in the relative proportions of gray and white matter, all of which are sensitive to gonadal steroids. Estrogens and androgens bind to receptors distributed throughout the cortex and influence dendritic growth, spine density, and glial development. By removing the steroid signal at its source, triptorelin appears to have removed one of the drivers of cortical expansion, while leaving subcortical and overall brain growth comparatively spared. The finding provides causal, experimental support for the idea that pubertal hormones actively shape cortical trajectories rather than merely coinciding with them.</p>
<p>The second imaging modality, diffusion-weighted magnetic resonance imaging, probed the microstructure of brain tissue by measuring how water molecules move through it. In the triptorelin-treated animals, diffusivity indices were increased in ways consistent with altered microstructural maturation. In the developing brain, falling diffusivity is typically interpreted as a signature of tissue organization: as axons become myelinated, as cells pack more densely, and as membranes proliferate, water movement becomes more constrained. Elevated diffusivity during a period when it should normally be declining therefore suggests that the normal cellular and architectural maturation of the tissue was delayed, slowed, or rerouted. The authors interpret these changes as evidence of altered microstructural development, a conclusion that dovetails with the cortical volume findings and points to the same underlying biology viewed through a different lens.</p>
<p>Perhaps the most novel contribution of the study comes from its metabolic arm. Using ex vivo proton high-resolution magic angle spinning spectroscopy, a technique that can quantify the chemical contents of tissue samples with exquisite sensitivity, the researchers examined the neurochemical profile of the treated brains. Long-term triptorelin treatment produced coordinated metabolic changes, most notably reduced levels of creatine and glutamine. Multivariate analyses, which look for patterns across many metabolites simultaneously, further identified creatine, glutamine, glutamate, and myoinositol as the key contributors separating the treated animals from controls.</p>
<p>Each of these metabolites tells a story. Creatine reflects the brain&#8217;s energy buffering system, serving as a reservoir for phosphate bonds that stabilize ATP supply; reduced creatine can indicate shifts in energy metabolism or in the density of metabolically active tissue. Glutamine and glutamate sit at the heart of the glutamate-glutamine cycle, the metabolic partnership between neurons and astrocytes that recycles the brain&#8217;s principal excitatory neurotransmitter; alterations in this pair suggest changes in excitatory neurotransmission or glial metabolism. Myoinositol, an osmolyte and glial marker, is often read as an index of astrocytic state and membrane-related signaling. That all four moved together, in a coordinated pattern that reliably distinguished treated from untreated animals, indicates that pubertal hormone suppression does not merely change brain shape but reconfigures the underlying neurochemistry of the developing cortex.</p>
<p>The authors frame their findings as providing a translational framework for interpreting structural and functional neuroimaging results in adolescents undergoing GnRHa treatment. This is a careful and consequential claim. Human studies of adolescents on puberty blockers have produced findings that are sometimes difficult to interpret, in part because it has been unclear which brain changes reflect the underlying condition, which reflect normal development, and which might reflect the treatment itself. By establishing, in a controlled animal model, that suppressing pubertal hormones attenuates cortical growth, alters tissue microstructure, and shifts the metabolic profile of the brain, the study supplies a mechanistic reference point against which human imaging findings can be benchmarked.</p>
<p>The work also carries broader implications for developmental neuroscience. Puberty is increasingly recognized as a second major window of synaptic and structural plasticity, comparable in importance to early postnatal development, and hormones are believed to be among its principal architects. This study demonstrates experimentally that removing the gonadal signal during this window leaves a measurable, multimodal imprint on the brain: smaller cortical volumes, altered diffusion characteristics, and a distinct neurochemical signature. It does not, and cannot, speak directly to the reversibility of these effects, to their functional or behavioral consequences, or to outcomes in humans, and the authors are appropriately measured in their interpretation. What it does establish is that the question is no longer speculative. Pubertal endocrine suppression measurably reshapes cortical developmental trajectories, and the tools now exist to map exactly how. As GnRHa treatment continues to be prescribed to adolescents around the world, studies of this kind, combining longitudinal imaging with molecular-level metabolic profiling, will be essential for building an evidence base robust enough to guide both clinical practice and the families navigating it.</p>
<p><strong>Subject of Research:</strong> Effects of pubertal hormone suppression with GnRHa on cortical structure and brain metabolism</p>
<p><strong>Article Title:</strong> Cortical and metabolic brain development during pubertal hormone suppression</p>
<p><strong>Article References:</strong> Marcos, A., González-Alday, R., Rodríguez del Cerro, M. C., Fernandez, R. M., Pásaro, E., Arias-Ramos, N., Zubiaurre-Elorza, L., López-Larrubia, P., &amp; Guillamon, A. (2026). Cortical and metabolic brain development during pubertal hormone suppression. <em>Translational Psychiatry</em>. <a href="https://doi.org/10.1038/s41398-026-04505-5" rel="noopener noreferrer">https://doi.org/10.1038/s41398-026-04505-5</a></p>
<p><strong>Image Credits:</strong> AI Generated</p>
<p><strong>DOI:</strong> <a href="https://doi.org/10.1038/s41398-026-04505-5" rel="noopener noreferrer">10.1038/s41398-026-04505-5</a></p>
<p><strong>Keywords:</strong> puberty blockers, GnRHa, triptorelin, cortical development, magnetic resonance imaging, diffusion imaging, MR spectroscopy, brain metabolism, glutamate, creatine, gender dysphoria, adolescent neurodevelopment</p>
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		<post-id xmlns="com-wordpress:feed-additions:1">257026</post-id>	</item>
		<item>
		<title>Korean Black Goat Meat Shows Lean, Unsaturated-Fat-Rich Profile With Age-Based Cut Choices</title>
		<link>https://scienmag.com/korean-black-goat-meat-shows-lean-unsaturated-fat-rich-profile-with-age-based-cut-choices/</link>
		
		<dc:creator><![CDATA[Daisy Hatcher]]></dc:creator>
		<pubDate>Mon, 05 Oct 2026 01:52:37 +0000</pubDate>
				<category><![CDATA[Agriculture]]></category>
		<category><![CDATA[age-specific meat cuts]]></category>
		<category><![CDATA[Aging]]></category>
		<category><![CDATA[anserine]]></category>
		<category><![CDATA[antioxidant properties of goat meat]]></category>
		<category><![CDATA[bioactive compounds]]></category>
		<category><![CDATA[bioactive compounds in goat meat]]></category>
		<category><![CDATA[carnosine]]></category>
		<category><![CDATA[creatine]]></category>
		<category><![CDATA[essential amino acids]]></category>
		<category><![CDATA[essential amino acids in goat meat]]></category>
		<category><![CDATA[fatty acids]]></category>
		<category><![CDATA[functional food]]></category>
		<category><![CDATA[health benefits of goat meat for different age groups]]></category>
		<category><![CDATA[indigenous Korean livestock]]></category>
		<category><![CDATA[Korean black goat meat]]></category>
		<category><![CDATA[Korean native black goat]]></category>
		<category><![CDATA[lean animal protein]]></category>
		<category><![CDATA[Meat Quality]]></category>
		<category><![CDATA[nutrition]]></category>
		<category><![CDATA[nutritional benefits of goat meat]]></category>
		<category><![CDATA[nutritional profiling of Capra hircus coreanae]]></category>
		<category><![CDATA[precision nutrition]]></category>
		<category><![CDATA[sustainable traditional Korean meats]]></category>
		<category><![CDATA[unsaturated fat-rich meat]]></category>
		<guid isPermaLink="false">https://scienmag.com/?p=236462</guid>

					<description><![CDATA[A new review finds that Korean native black goat meat is lean, rich in unsaturated fats, essential amino acids, and bioactive compounds, and proposes matching specific cuts to the nutritional needs of children, adults, and older adults.]]></description>
										<content:encoded><![CDATA[<p>Korean native black goats, a small indigenous breed known scientifically as Capra hircus coreanae, have long occupied a special place on the Korean table as a restorative food, yet their meat remains a niche product compared with beef, pork, and poultry. A new review published in Food Science of Animal Resources argues that this underused livestock species deserves fresh attention, not for tradition&#8217;s sake but because its meat displays an unusually favorable nutritional signature: lean flesh with minimal fat deposition, a fatty-acid balance tilted toward unsaturated fats, abundant essential amino acids, and a suite of bioactive compounds linked to antioxidant defense and energy metabolism. The authors, led by researchers at Gyeongsang National University, go a step further by proposing a cut-by-cut framework that matches specific parts of the animal to the nutritional priorities of children, adults, and older adults.</p>
<p>The review is careful about what it can and cannot claim. Because the evidence base for this breed is limited and heterogeneous, the authors screened 42 records published between January 2000 and January 2026 and retained 18 empirical studies as their core evidence, synthesizing the findings as a structured narrative rather than a meta-analysis. They explicitly frame their age-stratified suggestions as hypothesis-generating compositional alignments, not clinical dietary guidance. That caution matters, because most of the data come from laboratory profiling of meat composition rather than from controlled human trials, and the authors repeatedly warn that compositional plausibility is not the same as proven health benefit.</p>
<p>The physiological story begins with how these goats live. Korean native black goats are raised primarily as a meat breed, often under grazing-based systems in mountainous terrain. Their small body size and active foraging behavior are associated with limited fat deposition and a higher proportion of lean tissue. That leanness has a biochemical consequence: with less storage fat in the muscle, the overall lipid pool shifts toward membrane-associated polar lipids, which are typically richer in unsaturated fatty acids than the triacylglycerols that dominate fat depots. The result, according to the synthesis, is meat whose saturated fatty acid proportion hovers around 35 to 38 percent across major cuts, compared with figures approaching 45 percent in selected Hanwoo beef loin samples and exceeding 50 percent in a crossbred goat comparator.</p>
<p>Those numbers come with caveats. Fatty-acid composition is shaped by intramuscular fat levels, lipid-class distribution, breed, age, feeding system, muscle function, and postmortem handling, so cross-study comparisons are vulnerable to confounding. The review notes, for instance, that some pork cuts show saturated fat proportions as low as or lower than those of the goat leg cuts, and that marbling grade in beef reflects fatness and grain finishing as much as species identity. The consistent signal, the authors argue, is directional rather than quantitative: across shoulder, loin, foreleg, hind leg, and rib, Korean native black goat meat tends toward lower saturated and higher unsaturated fat than cattle, pigs, and crossbred goats, and even outperforms other goat crossbreeds. In the rib cut, the native goats measured 41.95 percent saturated fatty acids against 51.44 percent in the crossbred comparator.</p>
<p>Beyond the lipid profile, the meat is protein-dense in ways that matter for human nutrition. Its crude protein content is comparable to beef while its crude fat is exceptionally low, and its cholesterol level, roughly 35.73 to 37.48 milligrams per 100 grams, sits below typical beef or pork values. The meat is particularly rich in histidine, important for growth and tissue development, and arginine, which participates in ammonia detoxification and blood-flow regulation. It also carries high concentrations of L-carnitine, 20.8 to 26.0 milligrams per 100 grams, a compound that shuttles fatty acids into mitochondria for oxidation. Linoleic acid and oleic acid are the dominant unsaturated fatty acids, and linoleic acid serves as a precursor for eicosanoids that modulate inflammatory responses.</p>
<p>The most intriguing components may be the bioactive dipeptides and related metabolites. Creatine, carnosine, and anserine appear at notable levels, and each has a defined biochemical role: creatine supports rapid energy regeneration in muscle, carnosine buffers intracellular pH and mitigates oxidative stress, and anserine facilitates the removal of reactive oxygen species and recovery from muscle fatigue. These findings rest mainly on biochemical and experimental evidence, but they give the meat a functional profile that few mainstream livestock products can match. Rib cuts showed the highest antioxidant capacity among the major cuts in one analysis, while another study found the chuck, with its distinctive magnesium and phosphorus content, displayed the greatest antioxidative potential, suggesting that mineral composition may modulate antioxidant enzyme activity.</p>
<p>Cut-specific differences are where the review becomes genuinely practical. The hind leg is a branched-chain amino acid powerhouse, containing 2,672 milligrams of valine, 2,487 milligrams of leucine, and 1,565 milligrams of isoleucine per 100 grams, for a total of 6.72 grams, a substantial contribution toward World Health Organization reference intakes. It is also rich in the antioxidant amino acids histidine and methionine. The back loin, by contrast, has low collagen content and a favorable protein-to-unsaturated-fat ratio, making it tender and highly digestible, and it carries meaningful amounts of creatine, carnosine, and anserine. Rib meat is fattier but shows the strongest antioxidant activity in the assays used, while shoulder meat contains about 2.8 percent crude fat and notably high magnesium and phosphorus.</p>
<p>From these profiles the authors build their life-stage framework. For children and adolescents, whose rapid growth elevates protein and branched-chain amino acid requirements, the hind leg emerges as a plausible protein source supporting muscle accretion. For adults focused on cardiovascular and metabolic health, the loin or sirloin, with its lower saturated fat proportion and its creatine, carnosine, and anserine content, fits dietary patterns emphasizing a favorable fatty-acid balance; physically active adults might combine loin and hind leg cuts to support both protein synthesis and muscle energetics. For older adults, who face reduced protein digestibility and progressive muscle loss, the tender, easily chewed sirloin with its leucine-rich essential amino acid profile is the recommended starting point, while the dense hind leg may demand too much chewing and the fattier rib cuts warrant moderation.</p>
<p>The review situates these suggestions within established geriatric nutrition guidance, including the PROT-AGE position paper and ESPEN recommendations, stressing that protein needs in older people should be individualized according to health status, appetite, and comorbidities, with goat meat as one food-based option among many. It also confronts the sensory hurdle that has limited the breed&#8217;s market reach: the characteristic goaty odor, driven by volatile branched-chain fatty acids whose concentrations vary with genetics, age, feeding, and postmortem handling. Some consumers read that odor as traditional restorative value; others find it off-putting. Because the odor is a modifiable attribute rather than an immutable breed trait, the authors point to integrated control points spanning feeding, management, and processing, noting that high-pressure treatment has been reported to attenuate off-odor intensity, though commercial feasibility remains unproven.</p>
<p>The path forward, the authors conclude, requires coordinated work on several fronts: metabolic and genetic studies to explain how the goats&#8217; physiology produces their nutritional advantages; standardized cross-species comparisons normalized for intramuscular fat; controlled human trials measuring bioavailability and dose-response relationships for the bioactive compounds; pilot studies of protein digestibility and amino acid kinetics; and consumer research on acceptability and flavor reduction. Breeding programs are already underway, crossing three indigenous Korean lines with the New Zealand Boer breed to develop improved commercial strains. Until human intervention data arrive, the review&#8217;s message is measured but striking: a traditional medicinal meat may be one of the most nutritionally interesting protein sources in the modern livestock portfolio, provided consumers and scientists alike resist the temptation to treat compositional promise as clinical proof.</p>
<p><strong>Subject of Research:</strong> Nutritional composition of Korean native black goat meat and age-specific consumption strategies</p>
<p><strong>Article Title:</strong> Physiological and nutritional characteristics of Korean native black goats and their implications for age-specific consumption strategie</p>
<p><strong>Article References:</strong> Lee, H. W., Kim, W. J., Jang, H. G., Kim, D. B., Lee, H. J., Kim, J. H., &amp; Lee, S. Y. (2026). Physiological and nutritional characteristics of Korean native black goats and their implications for age-specific consumption strategie. <em>Food Science of Animal Resources, 46</em>(1), Article 51. <a href="https://doi.org/10.1007/s44463-026-00065-w" rel="noopener noreferrer">https://doi.org/10.1007/s44463-026-00065-w</a></p>
<p><strong>Image Credits:</strong> AI Generated</p>
<p><strong>DOI:</strong> <a href="https://doi.org/10.1007/s44463-026-00065-w" rel="noopener noreferrer">10.1007/s44463-026-00065-w</a></p>
<p><strong>Keywords:</strong> Korean native black goat, meat quality, fatty acids, essential amino acids, bioactive compounds, carnosine, anserine, creatine, nutrition, functional food, precision nutrition, aging</p>
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