Friday, May 03, 2024 | Last Update : 10:56 AM IST

  30 Sep 2023  Fragment 176-191 Peptide and Cartilage Research

Fragment 176-191 Peptide and Cartilage Research

SPOTLIGHT
Published : Sep 30, 2023, 5:11 pm IST
Updated : Sep 30, 2023, 5:11 pm IST

The precise workings of the mechanism by which Fragment 176-191 may exert its effect are a mystery

AOD 9604 was speculated to exhibit a potentially significant fat-burning impact when given to obese mice and beta(3)-AR knock-out mice for an extended period in a research published in 2001.  — By Arrangement
 AOD 9604 was speculated to exhibit a potentially significant fat-burning impact when given to obese mice and beta(3)-AR knock-out mice for an extended period in a research published in 2001. — By Arrangement

The natural growth hormone (HGH) has amino acids 176-191. The synthetic peptide Fragment 176-191 is identical to these amino acids. It is one of the various synthetic C-terminal segments of hGH examined for in vitro effects in rats. It has been speculated to decrease blood sugar without raising insulin-like growth factor 1 (IGF-1) or affecting insulin sensitivity, both of which are effects that are linked with exogenous hGH exposure [i].

There is not a lot of research that has been published on Fragment 176-191; thus, for researchers to acquire a better grasp of this peptide's mechanism of action, properties, and profile, they are turning to research that has been published on a fragment that is very similar, AOD 9604 (Fragment 177-191). After participating in several clinical tests, AOD 9604 has given researchers a clearer view of how synthetic C-terminal fragments may be presented and their potential effects [ii].

What Exactly Does Fragment 176-191 Work?

The precise workings of the mechanism by which Fragment 176-191 may exert its effect are a mystery, and research involving this peptide has received very little attention. As suggested by research, Fragment 176-191 has a mechanism of action similar to AOD 9604 due to its structural similarity [i]. AOD 9604 is a low-affinity agonist of the GH receptor that allegedly maintains some of the functions of GH without apparently triggering the pro-tumor and pro-diabetic consequences associated with GH presentation in animal research models [iii].

AOD 9604, acting as a GH receptor agonist, appears to work via binding to GH receptors and exhibits a GH-like impact on cartilage metabolism. This potential has been reported in research studies despite the hypothesis that AOD 9604 may not stimulate the proliferation of cells that have been transfected with the GH receptor, nor does it appear to stimulate the synthesis of IGF-1 [ii], [iv], [v]. As with AOD 9604, it is speculated that Fragment 176-191 may increase fat metabolism while raising energy intake, fat oxidation, and the production of myoblasts.

Fragment 176-191 Peptide Potential

The Fragment 176-191 that may be purchased online is only made accessible to trained researchers and is not designed for use in clinical trials involving humans. Researchers who are interested in the properties of Fragment 176-191 may examine the research and clinical trials that were done using the structurally similar peptide AOD 9604 and may find Fragment 176-191 for sale at Core Peptides.

Fragment 176-191 Peptide and Fat Studies

Fragment 176-191 of growth hormone (hGH) is usually referred to as the "lipolytic fragment" of hGH owing to the alleged fat-burning effects that were suggested in research studies conducted using murine models [i].

AOD 9604 was speculated to exhibit a potentially significant fat-burning impact when given to obese mice and beta(3)-AR knock-out mice for an extended period in a research published in 2001. After 14 days of presentation, the compound AOD 9604 was suggested to lower both the weight and the amount of body fat in the obese mice. It was determined that the alleged capacity of AOD 9604 to raise the synthesis of beta-3 adrenergic receptors (also known as ADRB3 in obese mice) may have been responsible for this finding. Notably, researchers speculated that neither lean mice nor genetically engineered mice (mice known as "beta(3)-AR knock-out mice") appeared to react to the lipolytic effects of AOD 9604 [vi].

As suggested by these results, a separate regulatory route for lipolysis may take precedence over the activity of ADRB3 when the animal’s body weight sits closer to its normal range. Because thermogenesis in skeletal muscle and fat burning in adipose tissue are two effects of ADRB3 that have been well studied, there is a significant amount of scientific interest in determining whether or not Fragment 176-191 may give comparable properties in research models.

Fragment 176-191 Peptide, Prediabetes, and Diabetes Type 2 Studies

There is interest in presenting Fragment 176-191 to research models in the hopes of furthering new avenues in prediabetes and type 2 diabetes research. Studies conducted on animals using six distinct segments of growth hormone (hGH; 172-191, 176-191, 177-191, 178-191, 179-191, and 180-191) indicated that the c-terminal end is likely responsible for the hypoglycemic action of the hormone. It was implied that Fragment 176-191 was the most efficient at reducing blood sugar levels out of the six evaluated segments. It appeared to have induced a prolonged rise in plasma insulin levels while simultaneously lowering insulin sensitivity, establishing a secondary potential in insulin resistance [i].

Fragment 176-191 Peptide and Cartilage Studies 

Researchers also consider that the hGH Fragment 176-191 may enhance cartilage repair. AOD 9604 was speculated to improve cartilage regeneration in a trial that was conducted in 2015 and included rabbits with collagenase-induced osteoarthritis of the knee. Researchers hypothesized that presenting HA and AOD 9604 together appeared more successful than giving either HA or AOD 9604 substance alone [vii]. It has been suggested that this peptide might develop more sophisticated methods for osteoarthritis and, in certain cases, could even do away with surgical intervention in the case of cartilege regeneration.

Disclaimer: No Asian Age journalist was involved in the creation of this content. The group also takes no responsibility for this content.

Tags: infocus