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Studi monyet menunjukkan infeksi Zika berkepanjangan pada kehamilan-T-REC semarang--komunitas reptil-semarang--KSE-komunitas satwa eksotik—komunitas semarang—komunitas reptil—komunitas reptil semarang—komunitas satwa—komunitas satwa semarang--berita artikel terkait tentang zika,kehamilan,studi monyet,monyet

01.16
Studi monyet menunjukkan infeksi Zika berkepanjangan pada kehamilan
Date:
June 28, 2016
Source:
University of Wisconsin-Madison
Summary:
Para peneliti mempelajari monyet yang telah menunjukkan bahwa salah satu infeksi virus Zika melindungi terhadap infeksi di masa depan , meskipun kehamilan dapat secara drastis memperpanjang waktu virus tetap dalam tubuh
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Peneliti dari University of Wisconsin - Madison mempelajari monyet yang telah menunjukkan bahwa
 salah satu infeksi virus Zika melindungi terhadap infeksi di masa depan , meskipun kehamilan
 dapat secara drastis memperpanjang waktu virus tetap dalam tubuh .
 
Para peneliti , dipimpin oleh UW - Madison patologi Profesor David O'Connor , menerbitkan
 sebuah studi dalam jurnal Nature Communications  yang menggambarkan pekerjaan mereka
 terhadap  kera di Wisconsin National Primate Research Center sebagai model untuk 
mempelajari cara infeksi virus Zika dapat berkembang di manusia.

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Monkey study shows Zika infection prolonged in pregnancy
Date:
June 28, 2016
Source:
University of Wisconsin-Madison
Summary:
Researchers studying monkeys have shown that one infection with Zika virus protects against future infection, though pregnancy may drastically prolong the time the virus stays in the body.
........................
University of Wisconsin-Madison researchers studying monkeys have shown that one infection with Zika virus protects against future infection, though pregnancy may drastically prolong the time the virus stays in the body.
The researchers, led by UW-Madison pathology Professor David O'Connor, published a study in the journal Nature Communications describing their work establishing rhesus macaque monkeys at the Wisconsin National Primate Research Center as a model for studying the way Zika virus infections may progress in people.
The team of UW and Duke University scientists -- which includes specialists in emergent and insect-borne diseases, genetics and immunology, pediatrics and pregnancy -- have been working with infected monkeys for months.
"What we've shown in the monkey model matches a lot of what people have observed in epidemiological studies of humans," says Emma Mohr, a pediatric infectious disease fellow at UW-Madison and first author on the study with Matthew Aliota and Dawn Dudley, research scientists in UW-Madison's schools of Veterinary Medicine and Medicine and Public Health, respectively.
"It's important for us to show in a lab setting what people have expected in humans -- that you clear viremia (infection by the Zika virus) within a week, and you are protected from future infections by the same virus."
The researchers infected monkeys with the type of Zika virus causing an epidemic that first became apparent in South America in 2015, and found that those monkeys resisted infection by the same Zika strain 10 weeks later.
"This is good news for vaccine design," says O'Connor, whose work is funded by the National Institutes of Health. "It suggests the sort of immunity that occurs naturally is sufficient. If you can mimic that in a vaccine, you'll likely have a very successful vaccine."
But their findings also uncovered a stark contrast in the length of infection of pregnant monkeys versus males and non-pregnant females. Though non-pregnant animals in the study were found to be free of Zika virus within 10 days of infection, the virus persisted in the blood of pregnant monkeys for 30 days to 70 days.
The prolonged infection has implications for the severe impacts of Zika virus during pregnancy. Zika has been tied to neurological problems in babies such as microcephaly, a particularly grim birth defect that results in underdeveloped brains and small heads.
"We have good news for most people: If you are not pregnant and not at risk of becoming pregnant, you probably don't need to be worried about Zika," O'Connor says. "But my concern for Zika virus in pregnancy is much higher now than it was six months ago."
One possible explanation for the persistence of the virus in pregnancy is that the immune systems of mothers-to-be are too compromised, and they simply aren't able to clear the virus as fast.
"The other, more provocative hypothesis is that it's indicative of infection of the fetus, and what we're observing in the maternal bloodstream is the shedding of virus by the fetus back into the mother's bloodstream," says O'Connor. "If that happens to be the case, it would suggest that there is a prolonged infection of the fetus that lasts much longer than the infection of the mother."
If the mother-fetus infection loop -- first proposed earlier this year by Johns Hopkins University obstetrician Rita W. Driggers in an analysis of Zika infection in a pregnant woman -- proves true, it could provide an opportunity to track the risks to a developing fetus without resorting to invasive (and also inherently risky) tests.
"If this is the case, measuring the viral load on a Zika-infected pregnant woman on a weekly or biweekly basis could provide an indication for the likely degree of damage to the fetus," O'Connor says. "If a pregnant woman comes into a clinic with Zika virus, but a week later shows no more evidence of infection, that could be a good indication that the fetus is unlikely to be affected."
Using the amount of virus in the blood of pregnant monkeys or women as a proxy for fetal infection might also provide researchers working on treatments to protect babies from neurological damage a way to assess their progress.
However, nobody really understands the range of outcomes for children that are affected by Zika virus infections during pregnancy.
"In Brazil, where the oldest children born to women who were infected with Zika are only about one year old right now, we don't have any idea whether some of the children who are apparently normal are going to have issues that only manifest later in life," O'Connor says.
According to the researchers, rhesus monkeys are often employed in brain research as models for humans.
"You may have to follow children for five years or longer to tell whether there is cognitive impairment in their development," says Aliota, whose research has focused on Zika's spread in Colombia. "But it's something you can answer with macaques relatively quickly, and that speed is very important in the context of an epidemic."
Though the researchers have been performing ultrasounds on Zika-infected pregnant monkeys and collecting fluid from their wombs, they can't yet say whether the still-growing fetuses themselves are infected or whether any of them are developing microcephaly.
"For human pregnancies, we have very refined growth charts, lots of historical information, lots of high-end diagnostic technologies that can be used to ask what's happening," O'Connor says. "While some of those things are in development in macaques, they are far less mature and far less detailed. So we can't draw conclusions yet."
But their results showing that one infection primes the immune system to protect against future infection could provide some peace of mind for millions left in the wake of the Zika epidemic.
"In Africa, where the virus has been circulating for an extended period of time, they haven't seen these adverse outcomes in pregnancy," Aliota says. "That seems to be because people are primarily exposed early in life, develop immunity, and then are protected later in life when they have children."

Story Source:
The above post is reprinted from materials provided byUniversity of Wisconsin-Madison. The original item was written by Chris Barncard. Note: Materials may be edited for content and length.

Journal Reference:
1.    Dawn M. Dudley, Matthew T. Aliota, Emma L. Mohr, Andrea M. Weiler, Gabrielle Lehrer-Brey, Kim L. Weisgrau, Mariel S. Mohns, Meghan E. Breitbach, Mustafa N. Rasheed, Christina M. Newman, Dane D. Gellerup, Louise H. Moncla, Jennifer Post, Nancy Schultz-Darken, Michele L. Schotzko, Jennifer M. Hayes, Josh A. Eudailey, M. Anthony Moody, Sallie R. Permar, Shelby L. O’Connor, Eva G. Rakasz, Heather A. Simmons, Saverio Capuano, Thaddeus G. Golos, Jorge E. Osorio, Thomas C. Friedrich, David H. O’Connor. A rhesus macaque model of Asian-lineage Zika virus infectionNature Communications, 2016; 7: 12204 DOI: 10.1038/ncomms12204



diet tinggi fruktosa selama kehamilan dapat membahayakan plasenta , membatasi pertumbuhan janin ---T-REC semarang--komunitas reptil-semarang--KSE-komunitas satwa eksotik--berita artikel terkait tentang diet fruktosa dan plasenta dan janin

02.12
diet tinggi fruktosa selama kehamilan dapat membahayakan plasenta , membatasi pertumbuhan janin
Obat yang diresepkan untuk mengobati asam urat , batu ginjal dapat meniadakan efek buruk gula ini
Date:
May 4, 2016
Source:
Washington University in St. Louis
Summary:
Penelitian pada tikus dan wanita menemukan bahwa mengkonsumsi diet tinggi fruktosa selama kehamilan dapat menyebabkan cacat pada plasenta dan membatasi pertumbuhan janin , berpotensi meningkatkan risiko bayi untuk masalah kesehatan metabolik di kemudian hari . Namun, allopurinol obat generik , sering diresepkan untuk mengobati asam urat dan batu ginjal , muncul untuk mengurangi dampak ibu dan janin negatif .
................
Mengkonsumsi diet tinggi fruktosa selama kehamilan dapat menyebabkan cacat pada plasenta dan membatasi pertumbuhan janin, berpotensi meningkatkan risiko bayi untuk masalah kesehatan metabolik di kemudian hari, menurut penelitian pada tikus dan orang-orang oleh  tim di Washington University School of Medicine di St . Louis.Namun, memberikan tikus allopurinol, obat generik yang sering diresepkan untuk mengobati asam urat dan batu ginjal, muncul untuk mengurangi dampak ibu dan janin negatif. Temuan menunjukkan dimungkinkan untuk merancang tes skrining dan rencana perawatan prenatal untuk wanita hamil dengan kadar fruktosa tinggi.

Penelitian ini tersedia secara online dalam Laporan Ilmiah, jurnal berafiliasi dengan Nature Publishing Group.
Fruktosa, gula alami dalam buah-buahan dan madu, telah populer selama beberapa dekade antara produsen makanan yang mengolahnya menjadi sirup jagung tinggi fruktosa yang digunakan untuk mempermanis makanan dan minuman. Bahkan, para peneliti telah melaporkan bahwa  gula rafinasi selama lebih dari setengah dari semua pemanis yang digunakan dalam rantai makanan-pasokan AS. Dan dalam beberapa tahun terakhir, ada kekhawatiran bahwa fruktosa dalam makanan olahan dan minuman manis mungkin berhubungan dengan diabetes dan obesitas.
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EXOTIC PETS COMMUNITY-- INDONESIA


Visit Our Community and Joint W/ Us....Welcome All Over The World
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High-fructose diet during pregnancy may harm placenta, restrict fetal growth
Drug prescribed to treat gout, kidney stones may negate the sugar's ill effects
Date:
May 4, 2016
Source:
Washington University in St. Louis
Summary:
Research in mice and women found that consuming a high-fructose diet during pregnancy may cause defects in the placenta and restrict fetal growth, potentially increasing a baby's risk for metabolic health problems later in life. However, the generic drug allopurinol, frequently prescribed to treat gout and kidney stones, appears to mitigate the negative maternal and fetal effects.
................
Consuming a high-fructose diet during pregnancy may cause defects in the placenta and restrict fetal growth, potentially increasing a baby's risk for metabolic health problems later in life, according to research in mice and people by a team at Washington University School of Medicine in St. Louis.
However, giving the mice allopurinol, a generic drug frequently prescribed to treat gout and kidney stones, appears to mitigate the negative maternal and fetal effects. The findings suggest it may be possible to devise a prenatal screening test and treatment plan for pregnant women with high fructose levels.
The study is available online in Scientific Reports, a journal affiliated with Nature Publishing Group.
Fructose, a sugar occurring naturally in fruits and honey, has been popular for decades among food manufacturers who process it into high-fructose corn syrup used to sweeten food and beverages. In fact, researchers have reported that the refined sugar accounts for more than half of all sweeteners used in the U.S. food-supply chain. And in recent years, there's growing concern that fructose in processed foods and sugary drinks may be linked to diabetes and obesity.
"Since the early 1970s, we've been eating more fructose than we should," said Kelle H. Moley, MD, the School of Medicine's James P. Crane Professor of Obstetrics and Gynecology and the study's senior author. "It is becoming increasingly critical to understand how fructose consumption is impacting human health. This study shows potentially negative effects of a high-fructose diet during pregnancy."
Fructose is processed differently than other sugars such as glucose, which the body converts into energy. Instead, fructose is broken down by liver cells that turn the sugar into a form of fat known as triglycerides while also driving high levels of uric acid, a normal waste product found in urine and stool. Too much uric acid can create metabolic mayhem resulting in obesity, type 2 diabetes and other health conditions.
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Fruktosa diproses secara berbeda dari gula lain seperti glukosa , yang mengubah  tubuh menjadi energi . Sebaliknya , fruktosa dipecah oleh sel-sel hati yang mengubah gula menjadi bentuk lemak yang dikenal sebagai trigliserida sementara juga pembawa  tingkat tinggi asam urat , produk limbah yang normal ditemukan dalam air seni dan tinja . Terlalu banyak asam urat dapat membuat kekacauan metabolisme yang mengakibatkan obesitas , diabetes tipe 2 dan kondisi kesehatan lainnya .

Studying mice, the researchers found elevated uric acid and triglycerides in otherwise healthy mice who were fed a high-fructose diet during pregnancy. Additionally, the mice developed smaller fetuses and larger placentas than those fed standard rodent chow.
Genetically, Moley said, a small fetus may become wired to grow more after birth than a normal-sized fetus. "The body tries to compensate for the small growth in utero," Moley said. "These babies can become kids and then adults struggling with obesity and other health problems."
Maternal health also may suffer. Metabolic problems caused by high levels of uric acid and fat increase a woman's risk of developing pregnancy complications such as preeclampsia -- a potentially serious condition in pregnancy often marked by high blood pressure, swelling and high protein levels in the urine -- and gestational diabetes, Moley said.
To assess the relevance of the mouse data in pregnant women, the researchers examined the association between fructose and placental uric acid levels in a small controlled group of 18 women who underwent scheduled cesarean sections. The women had no disorders that would have caused elevated uric acid. "We found a correlation suggesting similar maternal and fetal effects occur in humans," Moley said.
In the mouse model, researchers found that giving mice with high-fructose levels the common drug allopurinol -- a prescription medication that reduces uric acid -- reversed the refined sugar's negative maternal and fetal effects by reducing the levels of uric acid in the placenta.
"The negative effect of excess fructose in humans is likely to lead to an exacerbation of the problems seen in the mice," said Moley, who believes additional research may lead to a prenatal screening test for measuring fructose levels. This can be determined by simple blood work.
Besides advising pregnant women to limit fructose in their diets, treatment for those with high-fructose levels may include administering allopurinol, which crosses the placenta and generally is considered safe to take late in the second trimester or third trimester during pregnancy, Moley said.
"One of the best ways to ensure healthy maternal and fetal outcomes is by eating natural foods," she said. Future studies will test the effectiveness of giving allopurinol to pregnant women when there is concern about fetal growth, Moley added.
The study's lead author was Zeenat Asghar, a graduate student in molecular cell biology in the university's Division of Biology and Biomedical Sciences.

Story Source:
The above post is reprinted from materials provided byWashington University in St. LouisNote: Materials may be edited for content and length.

Journal Reference:
1.      Zeenat A. Asghar, Alysha Thompson, Maggie Chi, Andrew Cusumano, Suzanne Scheaffer, Noor Al-Hammadi, Jessica L. Saben, Kelle H. Moley. Maternal fructose drives placental uric acid production leading to adverse fetal outcomesScientific Reports, 2016; 6: 25091 DOI:10.1038/srep25091

Sumber :



Pedoman direvisi pada pengurangan risiko , pilihan pengobatan untuk penyakit tromboemboli pada kehamilan--T-REC-komunitas reptil-semarang--KSE-komunitas satwa eksotik

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More info :
www.trecsemarang2011.blogspot.com
minat gabung : ( menerima keanggotaan seluruh kota dan daerah di Indonesia )
08995557626
..................................
KSE – KOMUNITAS SATWA EKSOTIK – EXOTIC PETS COMMUNITY-- INDONESIA
Visit Our Community and Joint W/ Us....Welcome All Over The World
www.facebook.com/groups/komunitassatwaeksotik/
 KSE = KOMUNITAS SATWA EKSOTIK

MENGATASI KENDALA MINAT DAN JARAK

KAMI ADA DI TIAP KOTA DI INDONESIA
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Pedoman direvisi pada pengurangan risiko , pilihan pengobatan untuk penyakit tromboemboli pada kehamilan



Saran untuk mencegah dan mengobati tromboemboli vena ( VTE ) selama kehamilan , kelahiran dan setelah melahirkan diuraikan dalam dua pedoman baru  direvisi  . VTE jarang pada kehamilan atau dalam 6 minggu pertama postnatal dan risiko absolut sekitar 1 dari 1.000 kehamilan . Hal ini dapat terjadi pada setiap tahap kehamilan , tetapi saat risiko tertinggi adalah 6 minggu pertama setelah kelahiran , ketika risiko meningkat 20 kali lipat .....read more



Revised guidelines on reducing risk, treatment options for thromboembolic disease in pregnancy
Date:
April 16, 2015
Source:
Wiley
Summary:
Advice on preventing and treating venous thromboembolism (VTE) during pregnancy, birth and following delivery is outlined in two new revised guidelines. VTE is uncommon in pregnancy or in the first 6 weeks postnatally and the absolute risk is around 1 in 1,000 pregnancies. It can occur at any stage in pregnancy, but the time of the highest risk is the first 6 weeks following birth, when the risk increases 20-fold.
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advice on preventing and treating venous thromboembolism (VTE) during pregnancy, birth and following delivery is outlined in two new revised guidelines published by the Royal College of Obstetricians and Gynaecologists (RCOG) and launched at the RCOG World Congress in Brisbane, Australia.
VTE refers to the formation of a clot within veins. This can occur anywhere in the venous system, but the predominant sites are in the vessels of the leg (giving rise to deep vein thrombosis (DVT)) and in the lungs (resulting in a pulmonary embolism (PE)).
The Green-top Guidelines provide information, based on clinical evidence, to assist clinicians with both the prevention and treatment of VTE in pregnant women, a condition which remains the leading direct cause of maternal death in the UK.
VTE is uncommon in pregnancy or in the first 6 weeks postnatally and the absolute risk is around 1 in 1,000 pregnancies. It can occur at any stage in pregnancy, but the time of the highest risk is the first 6 weeks following birth, when the risk increases 20-fold.
Risk factors include previous VTE or thrombophilia (a tendency to form blood clots), obesity, increased maternal age, immobility and long-distance travel, admission to hospital during pregnancy and other comorbidities such as heart disease, inflammatory bowel disease and pre-eclampsia.
Additional risk factors occurring during the first trimester of pregnancy include hyperemesis gravidarum, ovarian hyperstimulation and IVF pregnancy. Caesarean section is also a risk factor.
The guidelines emphasise that all women should undergo a thorough assessment for VTE in early pregnancy or pre-pregnancy and again intrapartum or immediately postpartum.
Any woman with risk factors should be considered for prophylactic low-molecular-weight-heparin (LMWH), an injection administered to thin the blood. The duration of treatment depends on the number of risk factors a woman has. It may be offered both antenatally and after the baby is born.
In addition, women with previous VTE must be offered pre-pregnancy counselling. A prospective management plan for VTE should also be made, including appropriate treatment to be offered as early as possible and a careful history documented.
The guidance on treating VTE focuses on the acute management of the condition and highlights the signs and symptoms, including leg pain and swelling, lower abdominal pain, shortness of breath, chest pain, coughing blood and collapse.
Any woman presenting with signs and symptoms suggestive of VTE should be tested for the condition immediately and offered treatment with low-molecular-weight heparin (LMWH). All hospitals should have a protocol for the diagnosis of suspected VTE, with the involvement of a multi-disciplinary team of obstetricians, radiologists, physicians and haematologists.
Professor Catherine Nelson-Piercy, lead author of the guidance on preventing thromboembolism says: "Venous thromboembolism is rare in pregnancy and with prompt recognition can be treated effectively. This guidance provides clinicians with accurate scientific-based guidelines on the risk factors for VTE, as well as on how to prevent and treat the condition.
"It is vital that VTE is discussed with all women who are at risk and the reasons for individual treatment recommendations must also be explained."
Dr Andrew Thomson, lead author of the guideline on treating thromboembolism and co-Chair of the RCOG Guidelines Committee says: "Previous editions of these guidelines have been credited with a reduction in the number of women dying from thromboembolism during their pregnancy or in the postnatal period in the UK. Nonetheless, thromboembolism remains an important cause of maternal morbidity and mortality in our country.
"These updated guidelines provide new evidence about risk factors for thrombosis in pregnancy and strategies that should be employed to reduce the chances of a thrombosis occurring. Furthermore, the guidelines provide updated information on the way women with a suspected thrombosis should be investigated and treated."

Story Source:
The above story is based on materials provided by WileyNote: Materials may be edited for content and length.














 
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