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Herbs & Plants

Broom Moss

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Botanical Name :Dicranum scoparium
Family: Dicranaceae
Genus: Dicranum
Species: D. scoparium
Kingdom: Plantae
Division: Bryophyta
Class: Bryopsida
Subclass: Dicranidae
Order: Dicranales

Common Name :Broom Moss

Habitat :Broom Moss is native to North America, including the Great Lakes region.Grows on  Soil, humus, humus over rock, decaying stumps and logs, tree bases in dry to mesic woodlands.

Description:
Plants in loose to dense tufts, light to dark green, glossy to sometimes dull. Stems 2-10 cm, tomentose with white to brown rhizoids. Leaves very variable, usually falcate-secund, rarely straight and erect, slightly contorted and crisped when dry, sometimes slightly rugose or undulate, (4-)5-8.5(-15) × 0.8-1.8 mm, concave proximally, keeled above, lanceolate, apex acute to somewhat obtuse; margins strongly serrate in the distal 1/3 or rarely slightly serrulate; laminae 1-stratose; costa percurrent, excurrent, or ending before apex, 1/10-1/5 the width of the leaves at base, usually with 2-4 toothed ridges above on abaxial surface, with a row of guide cells, two thin stereid bands, adaxial epidermal layer of cells not differentiated, the abaxial layer interrupted by several enlarged cells that form part of the abaxial ridge, not extending to the apices; cell walls between lamina cells not bulging; leaf cells smooth; alar cells 2-stratose, well- differentiated, sometimes extending to costa; proximal laminal cells linear-rectangular, pitted, (25-)47-100(-132) × (5-)7-12(-13) µm; distal laminal cells shorter, broad, sinuose, pitted, (11-)27-43(-53) × (5-)8-12(-20) µm

Click to see the pictures…..…(01)......(1)……....(2).……....(3).…………………

Capsules mature spring.

Medicinal Uses:
The CH2Cl2 extract of Dicranum scoparium was found to possess pronounced antimicrobial activity against Bacillus cereus, Bacillus stearothermophilus, Bacillus subtilis, Staphylococcus aureus, and Escherichia coli.

Disclaimer:
The information presented herein is intended for educational purposes only. Individual results may vary, and before using any supplements, it is always advisable to consult with your own health care provider.

Resources:
http://en.wikipedia.org/wiki/Dicranum_scoparium
http://www.efloras.org/florataxon.aspx?flora_id=1&taxon_id=200000987
http://plants.usda.gov/java/profile?symbol=DISC71&photoID=disc71_005_ahp.jpg
http://www.herbnet.com/Herb%20Uses_AB.htm

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Ailmemts & Remedies Positive thinking

Toxic Shock Syndrome

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Definition:-
Toxic shock syndrome (TSS) is a very rare but potentially fatal illness caused by a bacterial toxin. Different bacterial toxins may cause toxic shock syndrome, depending on the situation. The causative bacteria include Staphylococcus aureus and Streptococcus pyogenes. Streptococcal TSS is sometimes referred to as toxic shock-like syndrome (TSLS) or Streptococcal Toxic Shock Syndrome (STSS).

TSS, is a serious condition which mainly affects menstruating women using tampons. The patient develops a high fever, diarrhea, vomiting and muscle ache. This is followed by hypotension (low blood pressure), which may eventually lead to shock and death. In some cases there may be a sunburn-like rash with skin peeling.

Experts are not sure why such a significant proportion of toxic shock syndrome patients are women who are menstruating and using a tampon – especially “super absorbent” tampons.

Toxic shock syndrome may also occur as a result of an injury, burn or as a complication of localized infections, such as a boil, as well as with the use of contraceptive sponges.

According to the National Health Service (NHS), UK, approximately 20 patients develop toxic shock syndrome each year in the United Kingdom, of which about 3 die. According to the Centers for Disease Control and Prevention (CDC), USA, toxic shock syndrome affects approximately 1 to 2 in every 100,000 women aged 15-44 years in the USA every year.

CLICK & SEE THE PICTURES

You may click to see the pictures of Toxic Shock Syndrome

Main Routes of infection:-
TSS can occur via the skin (e.g., cuts, surgery, burns), vagina (prolonged tampon exposure), or pharynx. However, most of the large number of individuals who are exposed to or colonized with toxin-producing strains of S. aureus or S. pyogenes do not develop toxic shock syndrome. One reason is that a large percentage of the population have protective antibodies against the toxins that cause TSS. It is not clear why the antibodies are present in people who have never had the disease, but likely that given these bacteria’s pervasiveness and presence in normal flora, minor cuts and such allow natural immunization on a large scale.

It is believed that approximately half the cases of staphylococcal TSS reported today are associated with tampon use during menstruation. However, TSS can also occur in children, men, and non-menstruating women.

Although scientists have recognized an association between TSS and tampon use, no firm causal link has been established. Research conducted by the CDC suggested that use of some high-absorbency tampons increased the risk of TSS in menstruating women. A few specific tampon designs and high-absorbency tampon materials were found to have some association with increased risk of TSS. These products and materials are no longer used in tampons sold in the U.S. (The materials include polyester, carboxymethylcellulose and polyacrylate). Tampons made with rayon do not appear to have a higher risk of TSS than cotton tampons of similar absorbency.

Toxin production by S. aureus requires a protein-rich environment, which is provided by the flow of menstrual blood, a neutral vaginal pH, which occurs during menstruation, and elevated oxygen levels, which are provided by the tampon that is inserted into the normally anaerobic vaginal environment. Although ulcerations have been reported in women using super-absorbent tampons, the link to menstrual TSS, if any, is unclear. The toxin implicated in menstrual TSS is capable of entering the bloodstream by crossing the vaginal wall in the absence of ulcerations. Women can avoid the risk of contracting TSS by choosing a tampon with the minimum absorbency needed to manage their menstrual flow and using tampons only during active menstruation. Alternately, a woman may choose to use a different kind of menstrual product that may eliminate or reduce the risk of TSS, such as a menstrual cup or sanitary napkin.

History:-
Initial description of toxic shock syndrome
The term toxic shock syndrome was first used in 1978 by a Denver pediatrician, Dr. James K. Todd, to describe the staphylococcal illness in three boys and four girls aged 8–17 years. Even though S. aureus was isolated from mucosal sites in the patients, bacteria could not be isolated from the blood, cerebrospinal fluid, or urine, raising suspicion that a toxin was involved. The authors of the study noted that reports of similar staphylococcal illnesses had appeared occasionally as far back as 1927. But the authors at the time failed to consider the possibility of a connection between toxic shock syndrome and tampon use, as three of the girls who were menstruating when the illness developed were using tampons. Many cases of TSS occurred after tampons were left in the woman using them.

Rely tampons:-
Following a controversial period of test marketing in Rochester, New York and Fort Wayne, Indiana, in August 1978 Procter and Gamble introduced superabsorbent Rely tampons to the United States market in response to women’s demands for tampons that could contain an entire menstrual flow without leaking or replacement. Rely used carboxymethylcellulose (CMC) and compressed beads of polyester for absorption. This tampon design could absorb nearly 20 times its own weight in fluid. Further, the tampon would “blossom” into a cup shape in the vagina in order to hold menstrual fluids without leakage.

Package of Rely Tampons

In January 1980, epidemiologists in Wisconsin and Minnesota reported the appearance of TSS, mostly in menstruating women, to the CDC. S. aureus was successfully cultured from most of the women. A CDC task force investigated the epidemic as the number of reported cases rose throughout the summer of 1980, accompanied by widespread publicity. In September 1980, the CDC reported that users of Rely were at increased risk for developing TSS.

On September 22, 1980, Procter and Gamble recalled Rely following release of the CDC report. As part of the voluntary recall, Procter and Gamble entered into a consent agreement with the FDA “providing for a program for notification to consumers and retrieval of the product from the market.” However, it was clear to other investigators that Rely was not the only culprit. Other regions of the United States saw increases in menstrual TSS before Rely was introduced. It was shown later that higher absorbency of tampons was associated with an increased risk for TSS, regardless of the chemical composition or the brand of the tampon. The sole exception was Rely, for which the risk for TSS was still higher when corrected for its absorbency. The ability of carboxymethylcellulose to filter the S. aureus toxin that causes TSS may account for the increased risk associated with Rely.

By the end of 1980, the number of TSS cases reported to the CDC began to decline. The reduced incidence was attributed not only to the removal of Rely from the market, but also to reduced use of all tampon brands. According to the Boston Women’s Health Book Collective, 942 women were diagnosed with tampon-related TSS in the USA from March 1980 to March 1981, 40 of whom died.

Symptoms:-
Symptoms of toxic shock syndrome vary depending on the underlying cause. TSS resulting from infection with the bacteria Staphylococcus aureus typically manifests in otherwise healthy individuals with high fever, accompanied by low blood pressure, malaise and confusion, which can rapidly progress to stupor, coma, and multi-organ failure. The characteristic rash, often seen early in the course of illness, resembles a sunburn, and can involve any region of the body, including the lips, mouth, eyes, palms and soles. In patients who survive the initial onslaught of the infection, the rash desquamates, or peels off, after 10–14 days.

Signs and symptoms of TSS (toxic shock syndrome) develop suddenly:
Sudden high fever (first symptom) The following signs and symptoms normally appear within a few hours:

*Vomiting
*Diarrhea
*Sunburn-like skin rash, particularly in the palms and soles
*Redness of eyes, mouth and throat
*Fainting
*Feeling faint
*Muscle aches
*Dizziness
*Confusion
*Hypotension (low blood pressure)
*Seizures
*Headaches

Causes of toxic shock syndrome :-
Scientists have been investigating the causes of TSS for over two decades and are still baffled. 20% to 30% of all humans carry the TSS causing bacterium, Staphylococcus aureus on their skin and nose; usually without any complications. Most of us have antibodies which protect us. Scientists believe that some of us do not develop the necessary antibodies.

Some experts suggest that the super-absorbent tampons – the ones that stay inside the body the longest – become breeding grounds for bacteria, while others believe the tampon fibers may scratch the vagina, making it possible for bacteria to get through and into the bloodstream. However, both are just theories without any compelling evidence to back them up.

We do know that the bacteria get into the body via wounds, localized infections, the vagina, the throat or burns. When the toxins (produced by the bacteria) enter the bloodstream they mess up the blood pressure regulating process, resulting in a hypotension (low blood pressure). Hypotension can cause dizziness and confusion (shock). The toxins also attack tissues, including organs and muscles. Kidney failure is a common TSS complication.

TSS does not only develop in young menstruating women. Older women, men and children may also be affected. Women who have been using a diaphragm or a contraceptive sponge have a slightly higher risk of developing TSS. In fact, anyone with a staph or strep infection has the potential to develop TSS (even though it is extremely rare).

Diagnosis:-
In contrast, TSS caused by the bacteria Streptococcus pyogenes, or TSLS, typically presents in people with pre-existing skin infections with the bacteria. These individuals often experience severe pain at the site of the skin infection, followed by rapid progression of symptoms as described above for TSS. In contrast to TSS caused by Staphylococcus, Streptococcal TSS less often involves a sunburn rash.

In either case, diagnosis is based strictly upon CDC criteria modified in 1981 after the initial surge in tampon-associated infections.:

1.Body temperature > 38.9 °C (102.02 °F)
2.Systolic blood pressure < 90 mmHg
3.Diffuse rash, intense erythroderma, blanching (“boiled lobster”) with subsequent desquamation, especially of the palms and soles
4.Involvement of three or more organ systems:

*Gastrointestinal (vomiting, diarrhea)
*Mucous membrane hyperemia (vaginal, oral, conjunctival)
*Renal failure (serum creatinine > 2x normal)
*Hepatic inflammation (AST, ALT > 2x normal)
*Thrombocytopenia (platelet count < 100,000 / mm³)
*CNS involvement (confusion without any focal neurological findings)

To date, there is no specific TSS test. The doctor needs to identify the most common symptoms, as well as checking for signs of organ failure.

*Blood and urine tests – these help determine organ function (or organ failure).

According to the National Health Service (NHS), UK, a confident TSS diagnosis can generally be made when:

*The patient’s temperature is above 38.9C (102.02F)
*The patient’s systolic blood pressure is below 90 mmHG
*The patient has a skin rash
*There is evidence that at least three organs have been affected by the infection

Pathogenesis:-
In both TSS (caused by Staph. aureus) and TSLS (caused by Strep. pyogenes), disease progression stems from a superantigen toxin that allows the non-specific binding of MHC II with T cell receptors, resulting in polyclonal T cell activation. In typical T cell recognition, an antigen is taken up by an antigen-presenting cell, processed, expressed on the cell surface in complex with class II major histocompatibility complex (MHC) in a groove formed by the alpha and beta chains of class II MHC, and recognized by an antigen-specific T cell receptor. By contrast, superantigens do not require processing by antigen-presenting cells but instead interact directly with the invariant region of the class II MHC molecule. In patients with TSS, up to 20% of the body’s T cells can be activated at one time. This polyclonal T-cell population causes a cytokine storm, followed by a multisystem disease. The toxin in S. aureus infections is Toxic Shock Syndrome Toxin-1, or TSST-1.

Treatment:-
The medical team’s aim is to fight the infection as well as supporting any body functions that the infection may have affected. The patient will be hospitalized and may be placed in an intensive care unit.

*Oxygen – the patient will usually be given oxygen to support breathing.

*Fluids – fluids will be administered to prevent dehydration and to bring blood pressure back up to normal.

*Kidneys – a dialysis machine will be used if there is kidney failure. The machine filters toxins and waste out of the bloodstream.

*Other damage – damage to skin, fingers or toes will need to be treated. This often involves draining and cleaning. In severe cases a body extremity or parts of skin may need to be surgically removed.

*Antibiotics – a combination of antibiotics is administered intravenously (directly into the bloodstream).

*Immunoglobulin – these are samples of donated human blood with high levels of antibodies which can fight the toxin. In some cases the medical team may administer immunoglobulin as well as antibiotics.
In the majority of cases the patient responds to treatment within a couple of days. However, he/she may have to stay in hospital for several weeks.

Click to see :->Streptococcal Toxic-Shock Syndrome: Spectrum of Disease, Pathogenesis, and New Concepts in Treatment

Prognosis :-
With proper treatment, patients usually recover in two to three weeks. The condition can, however, be fatal within hours.

Prevention:
Before going through about possible preventive measures, it is important to remember that the risk of developing TSS is very low. A significant number of experts point to a probably link between tampon absorbency and TSS risk, and advise women to:

*Thoroughly wash their hands before inserting a tampon
*Use the lowest absorbency tampons for their period flow
*Switch from tampons to sanitary towels (or panty liners) during their period
*Change tampons at least as regularly as directed on the pack
*Insert only one tampon at a time (never more than one)
*Insert a fresh tampon when going to bed and replace it immediately in the morning
*Remove the tampon as soon as the period has ended

The Mayo Clinic, USA, advises women to avoid using tampons completely when their flow is very light (use minipads instead).

The National Health Service (NHS), UK, advises that people who have had TSS should avoid using tampons.

Women who use a diaphragm, cap or contraceptive sponge should follow the manufacturer’s instructions carefully (regarding how long to leave the device inside the vagina). The NHS advises women who have had TSS to use an alternative method of contraception.

You may click & see also->

*Necrotizing fasciitis  :
*Septic shock    :
*Toxic headache :

Disclaimer: This information is not meant to be a substitute for professional medical advise or help. It is always best to consult with a Physician about serious health concerns. This information is in no way intended to diagnose or prescribe remedies.This is purely for educational purpose.

Resources:
http://en.wikipedia.org/wiki/Toxic_shock_syndrome
http://www.medicalnewstoday.com/articles/175736.php

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News on Health & Science

The New Bone Cement

New Bone Cement to Prevent Dangerous Injury Infections:-

…..
Osteomyelitis (OM) is a dangerous bacterial bone infection that often occurs in patients with open fractures. So it is not surprising that injured American soldiers serving in Afghanistan and Iraq have been getting OM, with an end result sometimes being a limb amputation. Now researchers from the Center for Musculoskeletal Research in Rochester with help from the Department of Orthopedics at Aarhus University Hospital in Denmark, Infectious Disease Service at Brooke Army Medical Center in San Antonio, and Heraeus Medical GmbH, created a new colistin-infused bone cement that is showing itself to be effective against the variety of bacterial pathogens that cause OM. Interestingly, Stryker already has a bone cement that features colistin, a product called Simplex P with Erythromycin & Colistin.

From a press statement by the University of Rochester Medical Center:
Not common in the United States and not potentially fatal, A. baumannii OM had been largely ignored until recently by physicians and the pharmaceutical industry, which focuses on life-threatening infections that affect millions, not hundreds. Then military outbreaks of the infection started among American soldiers returning from Iraq in 2003, with the number of A. baumannii OM infections seen in field hospitals, and in stateside facilities receiving injured soldiers, growing. At the same time, data began to emerge from hospitals treating soldiers suggesting that easily contracted A. baumannii may be arriving first at the fracture site and “priming” it so that it becomes more vulnerable to methicillin-resistant Staphylococcus aureus (MRSA), which recently surpassed HIV as the most deadly pathogen in the United States despite nearly universal use of the best available antibiotics.
“If you apply the findings from two small studies to the entire U.S. military, which is a leap, perhaps 2,000 soldiers come into field hospitals with compound fractures each year that become infected with A. baumannii,” said Edward Schwarz, Ph.D., professor of Orthopaedics within the Center for Musculoskeletal Research at the University of Rochester Medical Center. “About a third of them go on to get a staph infection after they reach the hospital, with about a third of those, perhaps 200 soldiers, suffering infectious complications that could cost them a limb. Studies already underway in our lab seek to clarify how the initial infections could gradually be replaced by catastrophic MRSA, and to prove that we can save limbs by putting an established antibiotic into bone cement for the first time.”

Approaches commonly used to overcome MDR [multi-drug resistant] infections after orthopaedic injuries include applying a large dose of antibiotic locally to the site of infection via bone cement. Bone cements composed of Plexiglas (polymethyl methacrylate or PMMA) have been used for decades for plastic surgery, to anchor in bone prostheses and to fill in holes in bone caused by trauma. Such materials became even more useful when researchers realized decades ago that they could load them with antibiotics to deliver large doses of drug directly to the injury site without subjecting the whole body to toxic levels of antibiotic. While bone cements laced antibiotics against staph and strep infections are common (e.g. vancomycin), no group had ever developed a bone cement treatment using colistin against A. baumannii.

Schwarz and colleagues developed a group of mice infected with drug resistant A. baumannii strains isolated directly from soldiers wounded in Iran and Afghanistan. The mice were then treated with either colistin by injection, local colistin via PMMA bead bone cement or a bone cement control with no drug.

Researchers measured the amount of bacteria in the mice as they responded to treatment with a new test of parC gene activity, a gene known to be present only in A. baumannii. Experiments confirmed that all study mice were infected with the bacteria, and that 75 percent of the strains were resistant to multiple antibiotics. Importantly, the bone cement containing colistin significantly reduced the infection rate such that only 29.2 percent of mice had detectable levels of parC after 19 days (p<0.05 vs. i.m. colistin and placebo). Colistin via injection failed to control the infection and was no better than placebo.

You may click to see:->

Press release: New Bone Cement May Prevent Amputations

Flashback: Rapid-Sequencing the Superbug

Sources:http://www.medgadget.com/archives/2009/01/new_bone_cement_to_prevent_dangerous_battle_injury_infections.html

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Herbs & Plants

White Leadwort

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Botanical Name:Plumbago zeylanica
Family:Plumbaginaceae
Parts used: roots, leaves;
Common Names in English:Cape Leadwort, White Plumbago
Common Name: chitra or chitraka, Chitrak, Agnimatha, Chitawa,

Habitat :This herbal plant is found throughout India. It grows wild as a garden plant in East, North and Southern India.

Description:
A much-branched shrub with long and tuberous roots and a striate stem (Plate 48). The leaves are up to 8 cm long, simple, glabrous, alternate, ovate or oblong, with an entire or wavy margin, an acute apex and a short petiole. The flowers are white in terminal spikes, with a tubular calyx, a slender, glandular, hairy corolla tube, with five lobes and five stamens, a slender style and a stigma with five branches. The fruit is a membranous capsule enclosed within the persistent calyx. The dried roots occur as cylindrical pieces of varying length, less than 1.25 cm in width, reddish-brown in colour with a brittle, fairly thick, shrivelled, smooth or irregularly fissured bark. The roots have a short fracture, an acrid and biting taste and disagreeable odour.

click to see the pictures.>…...(01).……(1)……...(2)..…...(3)..….(4)…..

Uses: in Ayurveda, pacifies kapha dosha (pungent, light, dry, sharp), anticancer, antifertility, anti-inflammatory, antimicrobial, anti-oxidant, prevention of antibiotic resistance, immunomodulator, anti-coagulant, abortifacient, vesicant, rheumatism, diarrhea, diuretic, skin conditions; precautions: pregnancy.

Medicinal uses:-
in Ayurveda, pacifies kapha dosha (pungent, light, dry, sharp), anticancer, antifertility, anti-inflammatory, antimicrobial, anti-oxidant, prevention of antibiotic resistance, immunomodulator, anti-coagulant, abortifacient, vesicant, rheumatism, diarrhea, diuretic, skin conditions; precautions: pregnancy.

In Ayurveda Chitra is used in treatment of various diseases and disorders. The chitrak root contains an acrid crystalline principle called ‘Plumbagin’ that is a powerful irritant and has well marked antiseptic properties. In small doses, the drug is a sudorific;

large doses cause death from respiratory failure. It is suggested that the action is probably due to the direct effect of the drug on the muscles. Chitrak root is also said to increase the digestive power and promote appetite and used in cases of enlarged spleen. A paste made from root is applied to abscesses to open them. Ayurvedic doctors recommend the root of chitrak for dyspepsia, piles, anasarca, diarrhea, skin diseases etc. It is also useful in colic, inflammations, cough, bronchitis, helminthiasis, haemorrhoids, elephantiasis, chronic and intermittent fever, leprosy, leucaderma, ring-worm, scabies, hepatosplenomegaly, amenorrhoea, odontalgia, vitiated conditions of vata and kapha and anaemia. The herb is also used as part of many ayurvedic compound remedies for rubifacient applications.

Anticancer activity: Plumbagin has been reported as having anticancer activity against fibrosarcoma induced by methyl cholanthrene and P388 lymphocytic leukaemia, but not against L1210 lymphoid leukaemia in mice. It is thought to be an inhibitor of mitosis. It has also been evaluated against Dalton’s ascitic lymphoma, where an inhibition of tumour growth and a significant enhancement of mean survival time were observed for treated mice compared to the control group. Peritoneal cell counts were also enhanced. Plumbagin­treated groups were able to reverse the changes in various haematological parameters which are a consequence of tumour inoculation. Studies have shown that plumbagin, when administered orally at a dose of 4 mg/kg body weight, caused tumour regression in rats with 3-methyl-4­dimethyl aminoazobenzene (3MeDAB)-induced hepatoma. It reduced levels of glycolytic enzymes such as hexokinase, phosphoglucoisomerase and aldolase levels, which are increased in hepatoma-bearing rats, and increased levels of gluconeogenic enzymes such as glucose­.6-phosphatase and fructose-I ,6-diphosphatase which are decreased in tumour hosts.

Antifertility activity: In rats, treatment during the first week of pregnancy abolished certain uterine proteins resulting in both pre­implantationary loss and abortion of the foetus. Uterine endopeptidases (cathepsin D, remin and chymotrypsin) were studied after the root powder had induced these effects and cathepsin D and renin activities were found to be decreased whilst chymotrypsin activity was increased. The results indicated that cathepsin D and renin may playa role in maintenance of pregnancy and chymotrypsin may be involved in postabortive involution. Plumbagin, at a dose of I and 2 mg/IOO g body weight, prevented implantation and induced abortion in albino rats without any teratogenic effects, and produced a significant inhibitory effect on copper acetate-induced ovulation in rabbits.

Antiinflammatory activity: A phosphate buffered saline extract of the roots of P. zrylanica stabilised red blood cells subjected to both heat- and hypotonic-induced lyses,A biphasic response and a reduction in the enzymatic activities of alkaline and acid phosphatases were observed and adenosine triphosphate activity was stimulated in liver homogenates of formaldehyde-induced arthritic rats.

Antimicrobial activity: A chloroform extract from P. zeylanica showed significant activity against penicillin- and non-penicillin resistant strains of Neisseria gonorrhoeae. It also showed antibacterial activity against Bacillus mycoides, B. pumilus, B. subtilis, Salmonella typhi, Staphylococcus aureus and others. Eye drops containing 50 llg/ml of plumbagin demonstrated significant antibacterial, antiviral and antichlamydial effects in eye diseases with few side effects. Aqueous, hexane and alcoholic extracts of the plant were found to show interesting antibacterial activity. The alcoholic extract was the most active and showed no toxicity when assayed using fresh sheep erythrocytes.

Antibiotic resistance modification: Plumbagin has been studied for its effect on the development of antibiotic resistance using sensitive strains of Escherichia coli and Staphylococcus aureus. When the organisms were inoculated into the antibiotic (streptomycin/rifampicin) medium, some growth was observed due to development of resistance. However, it was completely prevented when plumbagin was added to the medium and this was attributed to prevention of antibiotic resistance.

Antioxidant activity: At a concentration of 1 mM, plumbagin prevented peroxidation in liver and heart homogenates. By a comparison with menadione (which has one hydroxyl group less) it was suggested that plumbagin may prevent NADPH and ascorbate-induced microsomal lipid peroxidation by forming hydroquinones. These may trap free radical species involved in catalysing lipid peroxidation.

Immunomodulatory activity: The effect of plumbagin was studied on peritoneal macro phages of BALB/c mice, evaluated by bactericidal activity, hydrogen peroxide production and superoxide anion release. The bactericidal activity in vivo of plumbagin-treated mouse macrophages was estimated using Staphylococcus aureus and in low doses plumbagin caused a constant increase in bactericidal activity. It was also seen to exert a similar response on oxygen radical release, showing a correlation between oxygen radical release and bactericidal activity. Plumbagin appeared to augment macrophage bactericidal activity at low concentrations by potentiating oxygen radical release, whereas at higher concentrations it had an inhibitory effect.

Hypolipidaemic activity: When administered to hyperlipidaemic rabbits, plumbagin reduced serum cholesterol and LDL cholesterol by 53-86% and 61-91 % respectively. It also lowered the cho/esteroV phospholipid ratio and elevated HDL cholesterol significantly. Furthermore, plumbagin treatment prevented the accumulation of cholesterol and triglycerides in the liver and aorta and caused regression of atheromatous plaques of the thoracic and abdominal aorta. The animals treated with plumbagin excreted more faecal cholesterol and phospholipids.

Uterine stimulant activity: The juice extracted from the root was found to have potent activity when tested on rat uterus in vitro, as well as on isolated human
myometrial strips. This ecbolic effect was not blocked by either atropine sulphate or pentolinium bitartrate.

Anticoagulant activity: Plumbagin significantly increased prothrombin time, GPT, total protein and alkaline phosphatase levels in liver tissue and decreased GPT levels in serum. The anti-vitamin K activity was thought to be associated with the hydroxyl group attached to the naphthoquinone ring ofthe compound.

Digestive effects: The roots of Plumbago zeylanica were found to stimulate the proliferation of coliform bacteria in mice and act as an intestinal flora normaliser. This supports claims that the plant is a digestive stimulant.

Safety profile
The LDso of plumbagin is approximately 10 mg/kg body weight (oral and IP) in mice and a 50% alcoholic extract of the root or whole plant has an LD50 of 500 mg/kg body weight when given IP.26 In view of the documented abortifacient activity, it should be avoided at all stages of pregnancy.

Disclaimer:The information presented herein is intended for educational purposes only. Individual results may vary, and before using any supplements, it is always advisable to consult with your own health care provider.

Resources:
http://medical-dictionary.thefreedictionary.com/white+leadwort
http://www.india-shopping.net/india-ayurveda-products/Chitrak%20_WhiteLeadwort.htm
http://www.divineremedies.com/plumbago_zeylanica.htm
http://zipcodezoo.com/Plants/P/Plumbago_auriculata_Alba/

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How to Avoid Infections at the Gym

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gym, workoutHigh school, college, and pro athletes in sports including wrestling and baseball have come down with staph infections in recent years, in some cases MRSA, the potentially deadly strain that is immune to antibiotics. It’s not always clear where these and other infections originate, but athletes are at risk because they tend to get nicks and cuts, and also to share equipment and towels.

However, you can take some common-sense steps to protect yourself at the gym:

• Make sure the equipment is clean. Gyms are supposed to regularly clean off the equipment, but you should take your own precautions.

• Sharing is not always best. Don’t use someone else’s towel. In some cases, you may also get more peace of mind by purchasing your own basic equipment, like yoga mats.

• Shower right after you exercise. Don’t wait around in your sweaty clothes if you’ve been using common equipment or participating in a contact sport. Don’t use a communal bar of soap, either.

• Wear flip-flops or shower shoes when showering. While staph gets the headlines, athlete’s foot is still a pain. Protect yourself by keeping your feet off the communal shower floor.

• Think twice about the sauna or the whirlpool if you have a cut, scrape, or bad bruise. A couple of microbes thrive in hot water. If you do use a hot tub, shower afterwards.

Don’t ignore symptoms. Whether or not you’ve worked out lately, pay attention to a scratch, bruise, or cut that becomes red, hot, or tender.

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