Monday, 3 July 2017

Salvia miltiorrhiza (tanshinone IIA) kháng Bel-7402

Growth inhibition and apoptosis induction in human hepatoma cells by tanshinone II A.

Salvia miltiorrhiza (tanshinone IIA) kháng Bel-7402

From Wikipedia, the free encyclopedia
Salvia miltiorrhiza
Salviamiltiorrhiza.jpg
Scientific classification
Kingdom:Plantae
(unranked):Angiosperms
(unranked):Eudicots
(unranked):Asterids
Order:Lamiales
Family:Lamiaceae
Genus:Salvia
Species:S. miltiorrhiza
Binomial name
Salvia miltiorrhiza

Description[edit]

S. miltiorrhiza is a deciduous perennial with branching stems that are 30 to 60 cm (0.98 to 1.97 ft) tall, with widely spaced leaves that are both simple and divided. The 30 cm (0.98 ft) inflorescences are covered with hairs and sticky glands. Flowers grow in whorls, with light purple to lavender blue corollas that are approximately 2.5 cm (0.082 ft) long, with a dark purple calyx. Salvia miltiorrhiza

Uses[edit]

In traditional Chinese medicine[edit]

The outside of the taproot of Danshen, which is the part used in medicine is red.[8] Danshen is widely used in traditional Chinese medicine for treating chronic renal failure.[9] The root (Radix Salvia miltiorrhiza
Danshen is one of five ingredients in tangzhiqing (TZQ) used in traditional Chinese medicine for treating diabetes.[citation needed] In studies with mice and in vitro studies, TZQ and a modified formula known as TZQ-F have shown positive results.[11][12] The other ingredients of TZQ are red peony rootmulberry leaf, lotus leaf[citation needed], and hawthorn leaf.[11]

Chemical constituents[edit]

An antioxidant called salvianolic acid (or salvianolic acid B) isolated from Danshen is under study for protection against cerebrovascular disorders.[9][13]
Dihydrotanshinonetanshinone I, and tanshinone IIA are also under study for anti-cancer effects.[14][15]
Tanshinone IIA is one of the most abundant constituents of the root of Salvia miltiorrhiza

Pharmacological mechanisms[edit]

Results from animal and human studies support the use of Danshen for circulatory disorders to some extent because it is known to decrease the blood's ability to clot in at least two ways. First, it limits the stickiness of blood platelets.[medical citation needed] It also decreases the production of fibrin, the threads of protein that trap blood cells to form clots.[medical citation needed] Both these effects help to improve blood circulation. In addition, chemicals in danshen may relax and widen blood vessels, especially those around the heart.[medical citation needed] In animal studies, chemicals in danshen may also have protected the inner linings of arteries from damage. Some other research suggests it may increase the force of heartbeats and slow the heart rate slightly.[medical citation needed]
In animal studies, Danshen has appeared to interfere with the development of liver fibrosis — the formation of scar-like fibers in the liver.[24] Because the nonfunctioning fibers crowd out active liver tissue, liver function decreases gradually as the amount of fibrous tissue increases. Having chronic hepatitis and habitually drinking large amounts of alcoholic beverages are the major causes of liver fibrosis, which could also result from exposure to chemicals or certain drugs. Danshen may also increase blood flow into the liver,[medical citation needed] so the length of time that potentially damaging substances stay in the liver may be reduced, also reducing the possible injury they may cause. Results from a few animal studies showed it may also protect kidney tissues from damage caused by diabetes. In China, danshen has also been studied for treating acute pancreatitis, a painful and possibly dangerous inflammation of the pancreas.[25]
Danshen may stop the spread of several different cancer cell types by interrupting the cell division process[27] and also by causing cancer cells to undergo cell death (apoptosis).[15] In contrast, the cerebrovascular protective effect of Salvianolic acid has been found to be due to prevention of apoptosis.[9]
For HIV, chemicals in Danshen may block the effectiveness of an enzymeHIV-1 integrase, that the virus needs to replicate.[28]
Salvia may stimulate dopamine release and has protective effects against free radical-induced cell toxicity.[29][30]
S. miltiorrhiza stimulates increased osteogenesis (bone cell growth) in vitro .[31]
Salvianolic acid B could possibly facilitate the repair of tubular epithelial structures and the regression of renal fibrosis in injured kidneys.[32]

Drug Interactions[edit]

Danshen has been shown to potentiate the effects of the common anticoagulation drug warfarin, leading to gross anticoagulation and bleeding complications.Therefore, danshen should be avoided by those using warfarin.[8][33] Danshen causes in vitro interference when measuring digoxin levels when measured using Chemiluminescence Immunoassays (CLIA).[citation needed]

Platycodin D kháng Bel-7402

Platycodin D induces apoptosis and triggers ERK-and JNK-mediated autophagy in human hepatocellular carcinoma BEL-7402 cells

Platycodin D kháng Bel-7402

From Wikipedia, the free encyclopedia
Platycodin D
Platycodin D.png
Identifiers
PubChem CID
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references
Platycodin D is a bio-active isolate from roots of Platycodon grandiflorus. It has been studied for its spermicidal effects as a contraceptive in humans.[1]

Notes[edit]

References[edit]


Theaflavin kháng Bel-7402

The theaflavin monomers inhibit the cancer cells growth in vitro

Theaflavin kháng Bel-7402

From Wikipedia, the free encyclopedia
Theaflavin
Theaflavin.svg
Names
IUPAC name
3,4,5-Trihydroxy-1,8-bis[(2R,3R)-3,5,7-trihydroxy-2-chromanyl]-6-benzo[7]annulenone
Identifiers
3D model (JSmol)
ChemSpider
PubChem CID
UNII
Properties
C29H24O12
Molar mass564.50 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
 verify (what is Yes ?)
Infobox references
Theaflavin (TF) and its derivatives, known collectively as theaflavins, are antioxidant polyphenols that are formed from the condensation of flavan-3-ols in tea leaves during the enzymatic oxidation (sometimes erroneously referred to as fermentation) of black tea. Theaflavin-3-gallate, theaflavin-3'-gallate, theaflavin-3-3'-digallate are the main theaflavins.[1]Theaflavins are types of thearubigins, and are therefore reddish in color. Epigallocatechin gallate (EGCG) will metabolize into some theaflavins in the liver.[citation needed] Those molecules contain a tropolone moiety.

Research into health effects[edit]

HIV[edit]

In in vitro laboratory investigations, several tea polyphenols, especially those with galloyl moiety, can inhibit HIV-1 replication with multiple mechanisms of action. Theaflavin derivatives have been found to have more potent anti-HIV-1 activity than catechin derivatives.[2]
Epigallocatechin gallate (EGCG), a catechin in green tea, binds to gp120, which works in conjunction with gp41, itself blocked by TF-3 (a theaflavin), both receptors of which HIV hijacks to enter into healthy human immune cells.[citation needed]

Cholesterol[edit]

In a human clinical trial published in 2003, theaflavins were found to reduce blood cholesterol levels, both total and LDL.[3]

Cancer[edit]

In in vitro laboratory investigations, theaflavins have been found to act on numerous points regulating cancer cell growth, survival, and metastasis.[4] For example, TF-3 is a potent scavenger of superoxide.[5]