Tuesday, June 23, 2015

The Legitimacy of Holistic Admissions at U.S. Universities


With the competition for landing a quality job increasing with every passing year, acceptance into a high quality university is viewed as essential to maximizing the probability of landing one of these jobs. However, in lockstep with the competition for quality jobs, the competition to gain entrance into those universities widely regarded as high quality has also increased. This competition has produced controversy surrounding the procedure in which applicants are admitted creating a tug-of-war of sorts between various parties and their interests. One of the chief points of controversy is the validity of the “holistic” review process. In fact a lawsuit filled against Harvard University by the Students for Fair Admissions contends that holistic admission processes are inappropriately discriminatory and should be significantly clarified in their evaluation metrics beyond “whole person analysis”. Obviously a reading of the official complaint by the Students for Fair Admissions divulges a harsher conclusion than that above, but the sentiment above is more appropriate to produce a more fair admissions environment.

Proponents of the holistic method champion its multi-faceted analysis approach where a larger spectrum of an applicant’s qualifications for admissions is considered beyond the traditional metrics (standardized test scores, grades and certain extracurricular activities), which produces a more fair and accurate admissions process. Opponents of the holistic method believe that it is commonly used at best to hide the admissions process beyond a veil of ambiguity allowing universities to justify perplexing and arbitrary decisions and at worst to legitimize a quota system where more qualified candidates are rejected in favor of under-qualified candidates to achieve diversity demographics in order to evade public scorn. Clearly based on the perceived stakes, where getting into university A can set a person up for life versus university B which would create unnecessary hardships, the emotional aspect of this debate is high. Unfortunately this emotional aspect has produced an environment that abandoned a critical philosophical base for understanding the why or why not a holistic appropriate is appropriate.

First it is important to address that the holistic process has been attacked by some as a demonstration of “reverse racism” through the process of affirmative action. The term “reverse racism” is a misnomer and is not properly used in this descriptive context. Racism is giving differing treatment, either in a positive or negative manner, to an individual based on their ethnicity or race. Based on this definition, reverse racism would be akin to not giving differing treatment to an individual based on their ethnicity or race. However, when individuals invoke the term “reverse racism” the actual meaning is not what they are intending to convey. Instead they simply mean a different type of racism. Unfortunately some parts of society have associated the term racism to reflect only one particular form of racial bias instead of all forms of racial bias, which is inappropriate. Therefore, the term “reverse racism” should be eliminated from conversation in this context and replaced with the appropriate term – racism.

Second, it must be noted that the original intention of affirmative action was not to give “bonus points” to an individual based on their race, but to access how race may have influenced the acquisition of certain opportunities and thereby influenced the development of an individual through their performance when engaging in these opportunities. It should not be surprising that an individual with rich, committed and connected parents will have more opportunities and ability to prepare for those opportunities when presented than an individual without wealthy or even present parents.

For example it is expected that SAT scores would be higher for children of richer families both because of increased opportunity to prepare and increased opportunity to retest if the performance is not deemed acceptable. Also there is a higher probability that individuals from rich families will be better nourished than those individuals from poor families, which will directly influence academic performance and ability to participate in other valuable non-academic opportunities. Such environmental effectors are simple elements that can skew the value and analytical ability of “raw” metrics like standardized tests. Basically affirmative action is akin to judging the vault in gymnastics. Not all jumps have the same difficulty level; a non-perfect vault with a 10.0 difficulty will consistently beat a perfect vault with a 7.0 difficulty.

A quick side note: while the idea of affirmative action was originally based on the premise of race in an attempt to combat direct and indirect forms of racism, in the present the idea of affirmative action has shifted more to address differences in economic circumstance over race/ethnicity. The idea that rich individuals of race A will somehow be significantly excluded from opportunity A versus rich individuals of race B is modern society is no longer realistic. It is important to identify that more minorities will be assisted by affirmative action not directly because of race, but instead because of past racism that reduced the probability of these minority families to build intra-generational wealth thereby making them poorer than white families.

Based on the “potential judgment” aspect of affirmative action, some individuals may object to the idea that it is appropriate to punish an individual for having access to opportunities that others may not claiming that this behavior is a form of bias. This point creates the first significant philosophical question that must be addressed in the admissions process: is it justifiable that an above average individual in an advanced difficulty pool should find favor in an opportunity over a high quality performing individual in a lesser difficulty pool?

An apt example of this notion is seen in the disparity between the “Big 5” college conferences (ACC, Big 10, Big 12, PAC 12 and SEC) and the mid major conferences when selecting basketball teams for the NCAA Championship Tournament. While the committee tends to give preference to teams from the Big 5, the question is should they? A Big 5 power team, “Big Team A”, with a 55.5% conference winning percentage at 10-8 and an overall record of 21-13 has clearly demonstrated itself as slightly above-average among its peers whereas a mid major team, “Medium Team B”, with a 89% conference winning percentage at 16-2 and an overall record of 26-7 did not have the same opportunities to compete against the level of competition as Big Team A, but has demonstrated themselves a quality team with a greater unknown ceiling. Basically should someone slightly above the middle of the pack in one environment that could be viewed as more competitive be passed over for someone at the top at a tier 2 level?

In the arena of applicants the question of quality could boil down to: should the 100th best “area” A applicant be accepted over the 10th best “area” B applicant. Think about it this way: should applicant C from city y who scores significantly above average for that area on standardized tests and also has quality grades be accepted over applicant E from city x who scores slightly above average for that area on standardized tests and has quality grades even if applicant E’s scores are slightly higher? Note that obviously city x has a higher student average for standardized tests than city y.

Those who say yes to the above question based on the importance of fostering a racially/ethnically diverse environment must be careful not to fall into the trap of needless diversity, which is its own type of bias. With regards to fostering a diverse environment, its establishment must be based on thought and behavior, not on elements beyond an individual’s control.

There is an advantage to diversity of experience for it ensures a greater level of perspective and ability to produce understanding leading to more and potentially valid strategies for solving problems. However, this advantage comes from experience not from different skin color, religious beliefs, etc. For example the inclusion of person A just because he/she has certain colored skin or is of a certain ethnicity is not appropriate. Their inclusion should demand a meaningful and distinctive viewpoint. Cosmetic diversity for the sake of diversity serves no positive purpose and is inherently foolish and unfair/bias. Based on this point the crux of the issue regarding admissions is how to identify individuals with distinctive and valuable viewpoints in order to validate selecting a high achiever from a less difficult environment.

Most would argue that the standard analysis metrics are not appropriate for this task. For example grades are significantly arbitrary based on numerous uncontrollable environmental and academic circumstance; i.e. an A at high school x does not always carry the same weight as an A at high school y and some high schools allow students greater amounts of extra credit which conceal their actual knowledge of the subject through grade inflation. Standardized tests can be heavily prepared for and be taken multiple times depending on time and financial resources. Also they may not present an accurate representation of ability for almost no “real-world” task requires an individual to sit in one place in a time sensitive environment answering various questions without access to any outside resources beyond what is in their brain. At one point the “college essay” could have filled this role, but now it appears the essay has de-evolved into an ambiguous farce demanding only unoriginal “extraordinary” experiences and/or teaching moments where sadly it has become difficult to determine even if the student means what they say or are simply writing what they think the admissions officers want them to say.

However, while these flaws with the standard metrics exist, it is important to understand that abandoning the standard metrics entirely would be in error, for abandoning these metrics would be akin to replacing one “bias” with another. The standard metrics are an important puzzle piece, but they do not make up the entire puzzle.

For some the college interview has been thought of as a panacea for bridging the gap between holistic and standard admission judgment, but interviews do have caveats that must be monitored. Supporters of the interview process believe that it gives applicants an ability to demonstrate that he/she is more than just test scores, extracurricular activities and grades as well as allows both the university and applicant the ability to more specifically define the level of “fit” between the two beyond the mass generic questions utilized in the application process. Finally interviews can be a good deciding factor between board-line applicants.

Unfortunately interviews have some flaws that must be properly managed to ensure their legitimacy. First, individuals involved in the interview must be properly trained to avoid first impression bias as most interviews establish the tenor of the relationship between the interviewer and the interviewee very early, which threatens the objectivity of the rest of the interview. Also interviews must have a standard operating procedure, especially when it comes to the questions. Applicants must be asked the same questions for if different questions are asked to different applicants the subjectivity probability of the procedure increases, which hurts the interview as a comparison evaluation metric. It is fine to ask different questions if interviews are not going to be used when choosing one applicant over another, but most do not view the interview in such a causal light.

Another concern about the interview is they are unable to judge growth potential in how the university may positively or negatively influence the development of the applicant if he/she actually attends the university. Also if interviews do not have significant weight in the decision-making process then they may cause more harm than good due to lack of specific feedback providing more stress on an individual over relief as individuals wonder how the interview went leading to over-embellishment of the negative on small errors. Finally if interviews are deemed important it would be helpful if more universities offered travel vouchers to more financially needy applicants so if these individuals want to tour the campus and participate in the interview process they have an opportunity to do so that is not negatively impacted by their existing financially situation. Such a voucher may be important especially if interviews are used in “board-line” judgment.

A separate strategy may be the use of static philosophical probing questions in the application process. This strategy could better manage the difference in outside environmental influencing factors by gauging the general mindset of an applicant when it comes to solving problems. For example one question could be that if the individual were presented with a large jar full of chocolate and one individual sample; how would the individual calculate the number of chocolates in the jar? Note that this question demands both creativity and deterministic logic; creativity will produce more available options, but logic will be required to reason the best option from the list.

Another interesting question would be to ask what is the greatest invention in human history? Such a question would inspect whether an individual believes it is more important to build a foundation or if importance comes from what expands from that foundation. A third question could be what one opportunity would the applicant like to have had that they did not receive or was not available and why? These questions are superior to the generic banal analytically irrelevant questions that most universities ask on their admission forms.

Overall regardless of what methodology a university uses to accept or reject applicants the most important element is that this methodology is transparent. Universities must exhibit what attributes and credentials validate an individual’s merit for acceptance and then produce valid qualitative and quantitative reasons for why certain individuals gain admission and others do not. Transparency is the key element for a university to conduct their specific type of admission methodology without complaint. Returning to the original question whether or not a university elects to accept above average individuals from high “difficulty” environments or top performers from lower “difficulty” environment, either method is defensible as long as legitimate reasoning is available. However, there in lies the problem with the holistic method, universities are not transparent in its application, thus such behavior must change if a holistic method is to have any significant credibility.

Wednesday, June 10, 2015

Exploring the Biological Nature of Brown and Beige Fat

Over two years ago this blog discussed the possibility of incorporating a specialized preparation routine before exercise in an attempt to stimulate both brown and beige adipose tissue in order to increase the efficiency and overall calorie and fat burning potential of standard exercise. However, that post did not seek to fully understand or discuss the specific biological mechanisms that govern the behavior of brown or beige adipose tissue. This lack of knowledge limits the efficiency for exercise programs as individuals could either be consuming certain foods or performing certain warm-up tasks to increase exercise potential in addition to those suggested in the past blog post. Increasing exercise efficiency could be an easy means to increase the overall health of society without having to devote more precious time to exercise; therefore it would prove useful to better understand the processes that activate these types of fat.

At the most basic level there are two key elements to the fat burning capacity of brown fat. First, brown fat has multiple mitochondria versus the single mitochondria possessed by white fat; these additional mitochondria allow for greater rates of metabolism along with an increased lipid concentration. Also brown fat releases norepinephrine which reacts with lipases to breakdown fat into triglycerides and later to glycerol and non-esterified fatty acids finally producing CO2 and water, which can lead to a positive feedback mechanism.1,2 Second, brown fat contains significant expression rates of uncoupling protein 1 (UCP-1).1 UCP-1 is responsible for dissipating energy, which leads to the decoupling of ATP production and mitochondrial respiration.1 Basically UCP-1 returns protons after they have been pumped out of the mitochondria by the electron transport chain where these protons are released as heat instead of producing energy (i.e. leaking).

It is important to understand that there are two types of brown fat: natural brown fat and intermediate brown fat commonly known as beige fat. Natural brown is typically exemplified by the fat located in the interscapular region and contains cells from muscle-like myf5+ and pax7+ lineage.3 Natural brown fat is typically isolated from white fat and almost entirely synthesized in the prenatal stage of development as a means to produce heat apart from shivering.4 Beige fat is commonly interspaced within white fat, do not have these muscle-like cells (although Myh11 could be involved),5 and can be activated by thermogenic pathway and the strain of exercise. Beige fat also has the potential to influence the conversion of white fat to beige fat through a process commonly called “browning”.6,7

Natural brown fat is thought to have larger concentrations of UCP1-expression because they constitutively express it after differentiation versus beige, which expresses large amounts of UCP-1 in response to thermogenic or exercise cues.1,5 Therefore, natural brown fat is more effective at energy expenditure. However, it may not be possible to develop more natural brown fat after development; therefore, any positive progression in brown fat development will come from beige fat.

Early understanding of brown fat activation involved non-discriminate increases in the activity of the sympathetic nervous system (SNS). The standard pathway governing brown fat activation uses a thermogenic response involving the release of norepinephrine, which initiates cAMP-dependent protein kinase (PKA) and p38-MAPK signaling leading to the production of free fatty acids (FFA) through lipolysis due to UCP-1 induced proton uncoupling.4 UCP-1 concentrations are further increased through secondary pathways involving the phosphorylation of PPAR-gamma co-activator 1alpha (PGC1alpha), cAMP response element binding protein (CREB) and activating transcription factor 2 (ATF2).8 Among these three elements PGC1alpha appears to be the most important co-activating many transcription factors and playing an important role in linking oxidative metabolism and mitochondrial action.9

However, due to the complicated nature of SNS activation and its other downstream activators the attempt to replicate it in the form of weight loss drugs like Fenfluoramine or Ephedra resulted in severe negative cardiovascular side effects like elevated blood pressure and heart rate.10 While some argue that either increasing the sensitivity or the rate of simulation to the SNS can improve upon these results, the underlying elements associated with downstream activation of the SNS makes facilitating direct influence too complicated. Therefore, from a biological perspective it makes more sense to focus on a downstream element that interacts with brown fat at a more localized level.

Just a side note based on the differing interactivity between brown/beige and white fat from the SNS, white fat appears to represent long-term energy storage and brown fat is shorter-term energy, an unsurprising conclusion. However, frequent energy expenditure, like exercise, may condition the body to produce more beige fat versus white fat viewing short-term energy needs as more valuable than long-term energy needs. Basically if the above point is accurate then it stands to reason that a person would see more benefit from 20 minutes of exercise 6 days a week versus 40 minutes of exercise 3 days a week.

Moving away from direct SNS stimulation perhaps the appropriate method of increasing browning involves increasing transcription and translation of UCP1. Interestingly enough empirical evidence exists to support the idea that reinoic acid could be an effective inducer of UCP-1 gene transcription in mice and operates through a non-adrenergic pathway.11,12 However, a more focused study using loss of function techniques involving retinaldehyde dehydrogenase, which is responsible for converting retinal to retinoic acid, determined that retinal, not retinoic acid is the major inducer of brown fat activity.13 Unfortunately there is no direct understanding regarding the proportional response of brown fat to retinal or retinoic acid. Therefore, the general fat-soluble nature of vitamin A will probably make it difficult to utilize its derivatives as biological stimulants for brown fat activation or browning.

Another possible strategy to stimulate browning is through activated (type 2/M2) macrophages induced by eosinophils which are commonly triggered by IL-4 and IL-13 signaling. When activated this way these macrophages recruit around subcutaneous white fat and secrete catecholamines to facilitate browning in mice.14,15 A secondary means by which both IL-4 and IL-13 may influence fat conversion is their direct interaction with Th2 cytokines.16 Unfortunately while on its face this strategy looks promising, in a similar vein to vitamin A, it might not be effective due to unknown long-term side effects associated with IL-4 and IL-13 activation. Due to this lack of knowledge, if IL-4 or 13 is thought to be a viable biochemical strategy for inducing weight loss, long-term proper time lines for effects and dosages must be explored in humans, not just short-term studies in mice.

A more controversial agent in browning is fibronectin type III domain-containing protein 5 or more frequently known as irisin. Due to its significantly increased rate of secretion from muscle under the strain of exercise, some individuals believe that irisin is a key mediator in browning acting as a myokine;17 if this characterization is accurate then irisin could be a significant player in the biological benefits produced by exercise including weight loss, white fat conversion and reduced levels of inflammation.18,19 However, other parties believe that because human studies with irisin have produced results that do not demonstrate benefits similar to those studies using mice, irisin is another molecule that cannot scale-up its effectiveness when faced with the added biological complexity of humans versus a mouse.20-22

The key element within this controversy could be that irisin expression is augmented by the increased expression of PGC1alpha, but PGC1alpha increases the expression of many different proteins and other molecules, so the expression of irisin may not be relevant to the positive changes associated with exercise. Another factor may be that a key difference between mice and humans is the mutation in the start codon of the human gene involved in the production of irisin, which significantly reduces irisin availability.23 Thus this mutation could be the limiting factor to why despite a very conserved genetic sequence, humans do not see anywhere near the benefit mice do. If this explanation is correct it does potentially still leave the door open to directly inject irisin into the body to increase concentrations in an attempt to aid exercise derived results, but if PGC1alpha is the key, then this increased concentration of irisin could be of minimal consequence.

Another potential element that demonstrates a significant concentration increase in accordance to increased PGC1alpha is a hormone known as meteorin-like (Metrnl).24 The concentration of this hormone increases in both skeletal muscle and adipose tissue during exercise and exposure to cold temperatures in accordance to increases in PGC1alpha concentrations. When Metrnl circulates in the blood it seems to produce a widespread effect that induces browning resulting in a significant increase in energy expenditure.24 The influence of Metrnl on white fat does not appear due to direct interaction with the fat, but instead indirect action on various immune cells most notably M2 macrophages via the eosinophil pathway, which then interact with the fat through activation of various pro-thermogenic actions.24 As discussed above this interaction with eosinophil appears to function through IL-4 and IL-13 signaling indicating a common pathway purpose between IL-4/IL-13 and the original SNS pathway. Not surprisingly blocking Metrnl has a negative effect on the biological thermogenic response.24

Another potential strategy for browning may be targeting appropriate receptors instead of specific molecules; with this strategy in mind one potential target could be transient receptor potential vanilloid-4 (TRPV4). TRPV4 acts as a negative regulator for browning through its negative action against PGC1a and the thermogenic pathway in general.25 In addition TRPV4 appears to activate various pro-inflammatory genes that interact with white adipose tissue making it more difficult to facilitate browning even if the appropriate signals are present. TRPV4 inhibition and genetic ablation in mice significantly increase resistance to obesity and insulin resistance.25 The link between inflammation and thermogenesis is highlighted by the activity of TRPV4, which is one of the early triggers for immune cell chemoattraction.25

Obesity may also produce a positive feedback effect through TRPV4 by increasing cellular swelling and stretching through the ERK1/2 pathway, which increases the rate of TRPV4 activation.26,27 However, the validity of TRPV4 as a therapeutic target remains questionable for TRPV4 expression not only influences fat/energy expenditure, but also osmotic regulation, bone formation and plays some role in brain function.25,28,29 Fortunately a number of the issues with TRPV4 mutations/mis-function appear to be developmental in influence versus post-development, thus TRPV4 therapies could still be valid.

Natriuretic peptides (NPs) are hormones typically produced in the heart on two different operational capacities: atrial and ventricular. Both of these hormones appear to play a role in browning through association with the adrenergic pathway.30 The most compelling evidence for supporting this behavior is that a lack of NP clearance receptors demonstrated significant enhanced thermogenic gene expression in both white and brown adipose tissue.30 Also direct application of ventricular NP in mice increased energy expenditure.30 In addition to the above results, NPs are an inherent attractive therapeutic possibility because appropriate receptors are located in white and brown fat of both rats and humans31,32 and these receptors go through periods of significant decline in expression when exposed to fasting,33 which may account for some of the benefits seen from low calorie diets.

Atrial NPs increase lipolysis in human adipocytes similar to catecholamines (increasing cAMP levels and activation of PKA) although whether or not this increase is induced through interaction with beta-adrenergic receptors is unclear.34 Some believe that NPs activate the guanylyl cyclase containing NPRA producing the second messenger cGMP activating cGMP-dependent protein kinase (PKG).35,36 PKA and PKG have similar mechanisms for substrate phosphorylation including similar targets in adipocytes,36 thus this interaction may explain why atrial NPs act similar to catecholamines.

Recall from above that one of the means of inducing browning, especially for those tissues that are distant from SNS-based neurons, is macrophage recruitment. This recruitment appears to be initiated by CCR2 and IL-4 for when either is eliminated from mice models the conversion no longer occurs.15 Tyrosine hydroxylase (Th) is also important in this process facilitating the biosynthesis of catecholamines and later PKA levels.

With respects to producing a biomedical agent to enhance browning there appear to be three major pathways in play: 1) the SNS pathway producing a direct activation response; 2) macrophage recruitment pathway potentially involving Metrnl, which activates IL-4 and IL-13 eventually leading to PKA activation and an indirect activation response; 3) NPs activation pathway, which eventually leads to PKG activation and an indirect activation response. As mentioned earlier SNS pathway enhancement has already been attempted by at least two drugs and failed miserably, so that method is probably out. In addition the SNS pathway does not appear to have as much browning potential as the PKA or PKG pathways due to the reliance on the location of certain nerve fibers.

Enhancing macrophage recruitment could be a good strategy, but there appears to be little information regarding negative effects associated with short-term high frequency enhancement of IL-4 or IL-13 concentrations. Some reports have suggested an increase in allergic symptoms, but any more severe consequences are unknown. This is not to say that enhancing IL-4 or IL-13 is not a valid therapeutic strategy, but its overall value is unknown. In contrast enhancement of NPs appear to be a more stable choice due to positive results in initial exploration of both the application and the expected negative side effects. First, NPs can be administrated via the nose-brain pathway enabling access to the brain avoiding some potential systemic side effects.37 Second, there appear to be few, if any significant side effects to intranasal NP application, at least in the short-term.38

Overall the above discussion has merely identified some of the more promising candidates to enhance browning white fat. One could argue that resorting to drugs to enhance the overall health of an individual versus simple diet and exercise is a regretful strategy. Unfortunately the reality of modern society is that more and more people seem to have less available time to exercise or eat right. In addition to a mounting negative weight external environment (increased pollution and industrial chemicals like BPAs) this drug enhancement strategy may be the most time and economically efficient means to ensure proper weight control and overall health for the future.

Citations –

1. van Marken Lichtenbelt, W, et Al. “Cold-activated brown adipose tissue in healthy men.” The New England Journal of Medicine. 2009. 360:1500-08.

2. Lowell, B, and Spiegelman, B. “Towards a molecular understanding of adaptive thermogenesis.” Nature. 2000. 404:652-60.

3. Seale, P, et Al. “PRDM16 controls a brown fat/skeletal muscle switch.” Nature. 2008. 454:961–967.

4. Sidossis, L and Kajimura, S. “Brown and beige fat in humans: thermogenic adipocytes that control energy and glucose homeostasis.” J. Clin. Invest. 2015. 125(2):478-486.

5. Long, J, et Al. “A smooth muscle-like origin for beige adipocytes.” Cell Metab. 2014. 19(5):810–820.

6. Kajimura, S, and Saito, M. “A new era in brown adipose tissue biology: molecular control of brown fat development and energy homeostasis.” Annu Rev Physiol. 2014. 76:225–249.

7. Harms, M, and Seale, P. “Brown and beige fat: development, function and therapeutic potential.” Nat Med. 2013. 19(10):1252–1263.

8. Collins, S. “β-Adrenoceptor signaling networks in adipocytes for recruiting stored fat and energy expenditure.” Front Endocrinol (Lausanne). 2011. 2:102.

9. Handschin, C, and Spiegelman, B. “Peroxisome proliferatoractivated receptor gamma coactivator 1 coactivators, energy homeostasis, and metabolism.” Endocr. Rev. 2006. 27:728–735.

10. Yen, M, and Ewald, M. “Toxicity of weight loss agents.” J. Med. Toxicol. 2012. 8:145–152.

11. Alvarez, R, et Al. “A novel regulatory pathway of brown fat themogenesis, retinoic acid is transcriptional activator of the mitochondrial uncoupling protein gene.” J. Biol. Chem. 270:5666-5673.

12. Mercader, J, et Al. “Remodeling of white adipose tissue after retinoic acid administration in mice.” Endocrinology. 2006. 147:5325–5332.

13. Kiefer, F, et Al. “Retinaldehyde dehydrogenase 1 regulates a thermogenic program in white adipose tissue.” Nat. Med. 2012. 18:918–925.

14. Nguyen, K, et Al. “Alternatively activated macrophages produce catecholamines to sustain adaptive thermogenesis.” Nature. 2011. 480(7375):104–108.

15. Qiu, Y, et Al. “Eosinophils and type 2 cytokine signaling in macrophages orchestrate development of functional beige fat.” Cell. 2014. 157(6):1292–1308.

16. Stanya, K, et Al. “Direct control of hepatic glucose production by interleukins-13 in mice.” The Journal of Clinical Investigation. 2013. 123(1):261-271.

17. Pedersen, B, and Febbraio, M “Muscle as an endocrine organ: focus on muscle-derived interleukin-6.” Physiological Reviews. 2008. 88(4):1379–406.

18. Bostrom, P, et Al. “A PGC1-α-dependent myokine that drives brown-fat-like development of white fat and thermogenesis.” Nature. 2012. 481(7382):463–468.

19. Lee, P, et Al. “Irisin and FGF21 are cold-induced endocrine activators of brown fat function in humans.” Cell Metab. 2014. 19(2):302–309.

20. Erickson, H. “Irisin and FNDC5 in retrospect: An exercise hormone or a transmembrane receptor?” Adipocyte. 2013. 2(4):289-293.

21. Timmons, J, et Al. “Is irisin a human exercise gene?” Nature. 2012. 488(7413):E9-11.

22. Albrecht, E, et Al. “Irisin - a myth rather than an exercise-inducible myokine.” Scientific Reports. 2015. 5:8889.

23. Ivanov, I, et Al. “Identification of evolutionarily conserved non-AUG-initiated N-terminal extensions in human coding sequences.” Nucleic Acids Research. 2011. 39(10):4220-4234.

24. Rao, R, et Al. “Meteorin-like is a hormone that regulates immune-adipose interactions to increase beige fat thermogenesis.” Cell. 2014. 157:1279-1291.

25. Ye, L, et Al. “TRPV4 is a regulator of adipose oxidative metabolism, inflammation, and energy homeostasis.” Cell. 2012. 151:96-110.

26. Gao, X, Wu, L, and O’Neil, R. “Temperature-modulated diversity of TRPV4 channel gating: activation by physical stresses and phorbol ester derivatives through protein kinase C-dependent and -independent pathways.” J. Biol. Chem. 2003. 278:27129–27137.

27. Thodeti, C, et Al. “TRPV4 channels mediate cyclic strain-induced endothelial cell reorientation through integrin-to-integrin signaling.” Circ. Res. 2009. 104:1123–1130.

28. Masuyama, R, et Al. “TRPV4-mediated calcium influx regulates terminal differentiation of osteoclasts.” Cell Metab. 2008. 8:257–265.

29. Phelps, C, et Al. “Differential regulation of TRPV1, TRPV3, and TRPV4 sensitivity through a conserved binding site on the ankyrin repeat domain.” J. Biol. Chem. 2010. 285:731–740.

30. Bordicchia, M, et Al. “Cardiac natriuretic peptides act via p38 MAPK to induce the brown fat thermogenic program in mouse and human adipocytes.” The Journal of Clinical Investigation. 2012. 122(3):1022-1036.

31. Sarzani, R, et Al. “Comparative analysis of atrial natriuretic peptide receptor expression in rat tissues.” J Hypertens Suppl. 1993. 11(5):S214–215.

32. Sarzani, R, et Al. “Expression of natriuretic peptide receptors in human adipose and other tissues.” J Endocrinol Invest. 1996. 19(9):581–585.

33. Sarzani, R, et Al. “Fasting inhibits natriuretic peptides clearance receptor expression in rat adipose tissue.” J Hypertens. 1995. 13(11):1241–1246.

34. Sengenes, C, et Al. “Natriuretic peptides: a new lipolytic pathway in human adipocytes.” FASEB J. 2000. 14(10):1345–1351.

35. Potter, L, and Hunter, T. “Guanylyl cyclase-linked natriuretic peptide receptors: structure and regulation.” J Biol Chem. 2001. 276(9):6057–6060.

36. Sengenes, C, et Al. “Involvement of a cGMP-dependent pathway in the natriuretic peptide-mediated hormone-sensitive lipase phosphorylation in human adipocytes.” J Biol Chem. 2003. 278(49):48617–48626.

37. Illum, L. “Transport of drugs from nasal cavity to the central nervous system.” Eur. J. Pharm. Sci. 11:1-18.

38. Koopmann, A, et Al. “The impact of atrial natriuretic peptide on anxiety, stress and craving in patients with alcohol dependence.” Alcohol and Alcoholism. 2014. 49(3):282-286.