Management of Metabolic Syndrome*
Continue Reading : doi: 10.1002/mnfr.201400809
Continue Reading : doi.org/10.1016/j.jtcme.2022.01.001
c) Hepatic Steatosis
Elevated free fatty acids from adipose tissue and dietary intake are transported to the liver, and it stimulates de novo lipogenesis, ultimately leading to hepatic steatosis or fatty liver. Non-alcoholic fatty liver disease is a common liver disorder characterized by enlarged liver size and is mostly associated with obesity. In high fat-fed rats, administration of CurCousin™ induced lipolysis in differentiated adipocytes.
Administration of CurCousin™ resulted significant reduction in
– Hepatic triglycerides
– Lipid accumulation
– Inflammatory infiltration, and
– Ballooning degeneration of the liver
CurCousin™ helps to prevent and treat obesity and non-alcoholic fatty liver disease (Lai et al., 2015).
Continue Reading : doi: 10.1002/mnfr.201400809
d) Hyperlipidemia
Hyperlipidemia is a condition characterized by high lipid content in blood, especially non-HDL cholesterol and triglycerides, which may increase the risk of heart diseases.
Administration of CurCousin™ significantly reduced serum levels of total cholesterol and triglycerides in high-fat diet fed mice, indicating the effect of CurCousin™ on improving lipid homeostasis caused by the high-fat diet (Lai et al., 2015).
Continue Reading : doi: 10.1002/mnfr.201400809
e) Improved Serum Markers
Adipokines like leptin and adiponectin are the hormones produced by white adipose tissues, which play a pivotal role in the energy homeostasis processes. These adipokines also control metabolism and immunity.
CurCousin™ favorably modulates adipokines in high-fat diet fed mice (Figure 2). Notable modulatory properties of CurCousin™ included inhibition of leptin production, increase in adiponectin expression, and inhibition of local (adipocyte) and systemic inflammation caused by pro-inflammatory cytokines, like tumor necrosis factor alpha (TNF-α), interleukin (IL)-6 and IL-1ß (Unpublished observation).


Figure 2: Concentration of (A) adiponectin (ng/ml) (B) leptin (pg/ml) levels in serum of experimental animals
Other Benefits*
a) Prevention of Bone Damage
CurCousin™ effectively suppresses osteoclastogenesis induced by multiple myeloma and breast cancer cells via the inhibition of the NF-kB signaling pathway, which is mandatory for RANKL-induced osteoclastogenesis (Tyagi et al., 2016). Thus, CurCousin™ can effectively manage secondary bone lesions associated with cancer and nonmalignant diseases such as postmenopausal osteoporosis and rheumatoid arthritis.
Continue Reading : doi: 10.1016/j.abb.2016.02.013
b) Treatment of Arthritis
CurCousin™ showed potential protecting activity for mammalian articular cartilage from pathological damages in animal models. For inflammation studies, adjuvant arthritis was induced in Albino Wistar rats of either sex by the injection of heat-killed Mycobacterium tuberculosis and analyzed the effect of CurCousin™ in improving paw edema and associated markers. The in vivo studies revealed that CurCousin™ significantly reduced acute inflammation and edema in Carrageenan-induced rats (Table 1) (Unpublished observation).
Table 1: Effect of CurCousin™ on paw edema in adjuvant-induced arthritic rats
Test Materials | Doses (mg/kg p.o.) | %Inhibitory Activity |
---|---|---|
CurCousin™ | 2.5 | 19.21 % |
5 | 37.16 % | |
10 | 39.40 % | |
20 | 43.44 % | |
Acetyl salicylic acid (Standard) | 100 | 38.5 % |
Moreover, CurCousin™ could effectively modulate the cellular immune system by inhibiting the expression of CD4+ and CD8+ cells and associated cytokines and showed significant anti-arthritic activity.
*These statements have not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure, mitigate or prevent any disease.