Jaguar reveals ‘Type 00’ concept car, first under controversial new brand identity

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Image of Jaguar Type 00 concept vehicle
Jaguar

Famed British carmaker Jaguar revealed its new vehicle design direction Monday night with the introduction of an all-electric concept car called “Type 00.”

The vehicle, pronounced “Type Zero Zero,” features a minimalistic yet somewhat gaudy design. It is boxy with sleek lights and large wheels, a notably visual change from the brand’s current, sporty cars and SUVs.

Automakers routinely use concept vehicles to gauge customer interest in a design or show the future direction of a vehicle or brand. The vehicles are not meant to be sold to consumers.

Jaguar is expected to produce several new electric vehicles over the coming years, including a four-door GT car that is expected to be revealed next year that resembles the concept car.

Image of Jaguar Type 00 concept vehicle
Jaguar

Jaguar is projecting a range of up to 430 miles on a single charge with its new production EV, with up to 200 miles of range in 15 minutes when rapid charging.

The new concept vehicle comes weeks after Jaguar released an artistically flamboyant video meant to debut the company’s “Copy Nothing” rebranding.

The video featured androgynous models of varying ethnicities and sizes posing in vibrant clothing in a brightly colored landscape. The 30-second clip was accompanied by new logos and fonts for the embattled car company, a part of Tata Motors-owned group Jaguar Land Rover.

The rebrand and video went viral online, drawing widespread criticism on social media last month. The criticism ranged from commenters critiquing the company’s font choice and decision to remove the Jaguar animal logo — which has been featured on the car since the 1950s — to calling the company “woke” and saying it was abandoning its heritage.

Critics also noted that the ad did not have a car in the video. The company defended its efforts despite the backlash, saying the “brand relaunch for Jaguar is a bold and imaginative reinvention and as expected it has attracted attention and debate.”

The advertising campaign came after Jaguar in early November halted all new car sales in the U.K. as it prepares to relaunch as an electric-only company in 2026, part of a wider industry shift that is presenting numerous challenges for automakers.

Image of Jaguar Type 00 concept vehicle
Jaguar

Over the past few years, several automakers have announced plans to exclusively sell EVs, but many have backed off amid slower-than-expected adoption of the vehicles.

“We need to re-establish our brand and at a completely different price point so we need to act differently. We wanted to move away from traditional automotive stereotypes,” Jaguar managing director Rawdon Glover told the Financial Times in an interview last month.

Glover also condemned “the level of vile hatred and intolerance” expressed by some people commenting on the marketing video and denied it was “woke.”

CNBC’s Jenni Reid contributed to this report.

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27 Comments

  1. Our quest for an efficacious natural MSTN inhibitor
    within the form of a small molecule or short
    peptide is ongoing. This part will give a short understanding
    of screening natural compounds (Figure 2) and designing short peptides (Figure 3).
    Sulforaphane (SFN), which is found in cruciferous vegetables, is a bioactive isothiocyanate that inhibits the exercise of histone deacetylases (HDACs) (Myzak et al., 2006).
    SFN significantly reduces MSTN expression in porcine MSCs and can inhibit HDAC activities
    and DNA methyltransferase expression (Fan et al., 2012).
    This is an open-access article distributed under the phrases of the
    Inventive Commons Attribution License (CC BY).

    Skeletal muscle is a receptor tissue for androgens
    that positively influence muscle resilience, hypertrophy, and regeneration [91].
    Testosterone enhances muscular anabolism, accelerates protein era,
    prevents muscle breakdown, and boosts the effectiveness of amino acid reutilization in muscle tissue [92].
    Over 60% of people with severe CKD exhibit decreased blood concentrations of testosterone, which may set off muscle
    atrophy by modifying IGF-1 signaling and elevating myostatin quantities [92].
    Furthermore, female individuals with CKD have estrogen shortage
    within the first phase of the condition, and diminished estrogen concentrations correlate with decreased muscular strength and functionality [81].
    In a murine mannequin of CKD, parathyroid hormone and its receptor
    signaling in fats tissue induce dysregulated thermogenesis and
    hypermetabolism, resulting in muscle loss [86]. Consequently, human ranges of hormones also have a role in muscle atrophy among individuals with CKD.
    In addition to antagonizing the myostatin ligand, targeting its receptors to block the signaling transduction pathway has also been broadly explored as a treatment technique for muscle-loss issues.

    Upon reaching 80% confluence, the cells had been switched to
    DMEM containing 2% horse serum to provoke differentiation for four
    days, with the medium being refreshed each other day. After
    completing rigorous train, we measured LG ranges in the liver and MG ranges within the gastrocnemius muscle.
    Moreover, we measured the LA, CK, LDH, BUN, SOD,
    and MDA levels in the serum using the desired kits, following the manufacturer’s directions.

    Hippocampal tissue homogenates have been rapidly ready in an ice tub
    and centrifuged at 12,000 rpm for 10 min at 4 °C to collect the supernatant.

    Further research is required to completely elucidate
    the interactions between MSTN inhibition and metabolic disorders.
    Fatigue has turn into increasingly frequent and significant with societal progress and
    faster pace of life. Fatigue is a complex physiological and
    biochemical process that occurs when brain or physical strength reaches a sure stage1.

    When mixed with a proper food plan and exercise routine, dietary supplements containing these elements may help break by
    way of development plateaus and enhance both muscle
    size and power. Always consult with a healthcare professional before starting any
    new supplement routine, particularly when you have underlying health conditions
    or are taking different drugs. Stamulumab (Myo-29), developed by Wyeth Pharmaceuticals (now Pfizer),
    is the first myostatin inhibitor to progress to medical trials.

    Myo-29 is a monoclonal anti-myostatin anti-body designed to deal with sufferers with
    Becker muscular dystrophy, facioscapulohumeral muscular dystrophy (FSHD),
    or limb-girdle muscular dystrophy (LGMD).

    Regardless Of encouraging outcomes of the preclinical studies [59] and safety profile,
    Myo-29 failed to point out vital enhancements in muscle power or perform probably as a
    outcome of excessive fee of clearance [60], which halted its additional development.
    Myostatin-induced phosphorylation of Smad3 interferes with the activity of MyoD,
    a grasp transcription factor in myogenesis, impairing myoblast
    differentiation [35].
    A case examine of a human baby with unusually high ranges of muscle development reported that the kid also had very low levels
    of myostatin. The authors advised that myostatin inhibition could have been concerned in the observed
    enhanced muscle progress, although no other comparable instances have been reported [18].
    First, some proof suggests that inhibiting myostatin can forestall muscle from weakening during long durations of inactivity.
    For instance, myostatin inhibition decreased the lack of muscle in young mice that were
    prevented from using their hind legs for 21 days [11].
    In the muscular tissues, extra glucose means extra vitality that
    enhances efficiency and muscle constructing. It acts on granulosa cells to trigger
    the release of progesterone, minimizing the fluctuations in the menstrual cycle.
    Research targeted on follistatin 344 as a potential most cancers remedy counsel that it negatively impacts certain cancers such as the prostate,
    esophagus, and pores and skin (7). Perhaps, probably the most ground-breaking findings of mice-based
    studies counsel that follistatin 344 may help in some
    particular forms of most cancers remedy. Some myostatin inhibitors have progressed into scientific improvement as summarized in Table 1.
    There has been progress in evaluating antimyostatin therapies
    in animal fashions of muscle wasting problems.
    Some packages have progressed into medical growth with initial outcomes exhibiting
    optimistic influence on muscle volume.
    We additionally measured biochemical indicators, together with LG, MG, LA, CK, LDH,
    and BUN ranges, to assess fatigue. Previous analysis
    has highlighted the significance of glycogen as an power supply throughout train, with adequate hepatic glycogen and myoglycogen enhancing endurance and sustaining high-intensity
    exercise18,19,20. LA is a key indicator for assessing fatigue ranges as it is the finish product of
    anaerobic glycolysis during high-intensity exercise.
    This course of can lead to a lower within the muscle and
    blood pH, which may trigger tissue injury and elevated fatigue21,
    22. Elevated LDH and CK levels reflect skeletal muscle cell necrosis and tissue damage23,24.

    When fatigue arises from high-intensity exercise, insufficient
    vitality from carbohydrate and fats metabolism
    happens, leading to protein and amino acid
    depletion and elevated urea nitrogen levels22.
    By using Epicatechin as a dietary supplement, the brand suggests that you may discover improvements in restoration, increased ranges of antioxidant help,
    and reductions in myostatin levels, which in flip, will increase follistatin. Various myostatin inhibitor dietary supplements,
    similar to protein powders, dark chocolate, Vitamin D, epicatechin dietary supplements, and egg yolk supplements, have been proposed to lower myostatin. The
    present research suggests no concrete proof that myostatin dietary supplements are needed.

    Thus, Epi is the primary compound ever famous, to favorably
    modulate each regulators of muscle growth and recommend increases in energy.
    From a biomedical perspective, myostatin inhibitors are a kind of drug that target myostatin, a protein involved in regulating muscle development and
    development. Myostatin inhibitors work by blocking the exercise of myostatin, which may result in increased muscle mass and energy.
    These inhibitors have potential purposes in treating muscle-wasting conditions, such
    as muscular dystrophy, and may also be used to reinforce muscle growth in athletes and
    bodybuilders. By inhibiting myostatin, these medication can promote muscle hypertrophy and probably improve muscle
    operate.
    This is essential as a result of previous a certain size, including more mass to muscle tissue doesn’t actually make them stronger –
    and muscular tissues which may be too giant are also extra vulnerable to wreck.

    Over-developed muscle tissue also can get in the means in which
    of other essential organs, decreasing their dimension and
    impairing their features [1, 2]. PureRawz provides a high-quality peptide solution that’s ideal for these exploring the benefits of
    myostatin inhibitors.
    Moreover, the present analysis doesn’t again the efficacy
    of myostatin inhibitor supplements for enhancing muscle improvement.
    If you missed the first article on myostatin and resistance train on Proof Primarily
    Based Muscle, you can find it here. Briefly, the article mentioned that gentle and heavy-weight
    exercises resulted in similar muscle gene responses to train, including myostatin. Myostatin is
    a category of growth components genes that put the automotive breaks muscle progress.
    Myostatin is a class of growth differentiation components
    that regulate muscle growth. Different attainable
    side effects of myostatin inhibitors include increased
    the possibility of tendon rupture, coronary heart failure as a end result of inflamed cardiac muscle, and rhabdomyolysis, a breakdown of
    muscle fibers that often results in kidney failure
    [38, 39].
    This good little study actually highlights the already well documented body of evidence that’s led many
    scientists and experts to consider creatine is anabolic while Leucine and
    HMB are anti-catabolic. Properly, that’s
    best answered by speaking about the different three dietary supplements, I
    talked about earlier in this article. It’s been discontinued now,
    but MYO-X might be the bodybuilding world’s most
    well known patented myostatin inhibitor. So, scientists have
    identified tips on how to inhibit myostatin in animal studies for a really long time now
    and they’ve experimented with different ways of doing it, and at totally
    different phases within the life-cycle. The data on this
    website has not been evaluated by the Meals & Drug Administration or some other medical
    physique. You must seek the guidance of your doctor earlier than appearing on any content
    material on this website, especially if you’re pregnant, nursing, taking
    medicine, or have a medical situation. The opinions expressed on this part are solely those
    of the users who could or may not have medical or scientific training.

    Indeed, myostatin is considered a highly druggable target and the current research
    demonstrates a possible novel dietary approach for its modulation that negates prior problems with poor ET/EA bioavailability.

    Polyphenolic plant extracts have demonstrated anti-inflammatory
    and anti-catabolic results in vitro, nonetheless their significant translation into humans remains elusive.
    Urolithin A (UA), a gut-derived metabolite of ellagitannins, has proven promise for bettering muscle operate and metabolic well being in rodent models.
    This research aimed to discover the influence of UA on insulin and anabolic sensitivity in human skeletal muscle cells.

    Follistatin (FST) and its related FST-type molecules are naturally antagonists to several TGF-β proteins, and are widely
    known inhibitors of MSTN [70, 71]. FST binds to mature MSTN with high affinity
    and inhibits its binding to ActRIIB, but doesn’t interact with proMSTN [20, 72].

    The N-terminal α-helical domain of FST interacts immediately with a sort I receptor binding site
    of MSTN, inflicting inactivation [73]. Consequently, FST lacking its C-terminal peptide or fragments of the N-terminal region show comparable inhibitory
    results [73–75].
    Intransgenic mice overexpressing FST exhibit decreased
    quality of skeleton and tibia fractures in contrast to myostatin null mice that show enhanced BMD with out fractures (Fig.
    2) [6]. Above all, these findings strongly emphasize the importance of target specificity
    when growing myostatin inhibitors, particularly these intended for long-term therapy, to attenuate potential antagonistic results in different tissues.
    ACE-011 in a section 1 clinical trial carried out on wholesome postmenopausal ladies additionally elevated hematocrit, Hb,
    and RBC levels [56]. These results have evoked a considerable interest in ACE-011,
    initially developed to treat bone-loss problems,
    as a potential therapeutic option for patients with anemia and illnesses involving ineffective
    erythropoiesis.
    The product offers them a feeling of nothing being heavy and stamina like they have
    not had, and they really feel they’ll go longer at the
    health club and do not have to wait too lengthy in between. They
    really feel nice daily, have better humor and power, and experience reduced appetite,
    improved sleep quality, and better restoration. C2C12
    cells were seeded into culture dishes, processed, and
    harvested in accordance with the aforementioned protocol. Subsequently, LDH,
    SOD, and MDA actions in cells were assessed based on the manufacturer’s tips.

    Some common names for ecdysterone embrace ecdisten, ecdysone, isoinokosterone, 20-hdroxyecdysone and β-ecdysterone.
    Despite these potential benefits, no analysis has supported these
    claims in human models. One Other class of MSTN inhibitors is fusion proteins, usually within the form of soluble activin receptors, which act as ligand
    traps by binding MSTN and preventing its additional interactions.
    Acceleron, now owned by Merck, first introduced ligand traps to medical
    trials with ramatercept in 2008. Ramatercept is a fusion protein consisting of
    human IgG linked to the extracellular domain of ActRIIB, acting as a soluble form of ActRIIB,
    which binds MSTN and other TGF-β members. In a part 1 trial
    involving women, complete muscle volume (TMV) was improved by roughly 5.1% following
    a single injection of three mg/kg [62].
    It is a monoclonal antibody with an IgG4 Fc area designed for
    sarcopenia and inclusion body myositis (IBM) treatment.
    Trevogrumab targets MSTN in its mature, latent, and pro-forms without cross-reactive binding to GDF11 [57].
    Apitegromab, developed by Scholar Rock, particularly targets MSTN in its latent type by stabilizing its conformation, thereby stopping entry to prodomain protease
    cleavage sites [58, 59]. Apitegromab has proven efficacy in rising muscle mass and function in mouse fashions
    of spinal muscular atrophy (SMA) [60].
    Investigations have established that CKD is accompanied
    by mitochondrial impairment, a discovering that is also seen in the aged [27].
    Dynamin-related protein 1 (DRP-1) is an indicator
    of mitochondrial fission that sustains mitochondrial normal situations.
    Microarray analysis of people with CKD, together with these present process hemodialysis, has indicated
    a compromised mitochondrial respiratory perform and consequent oxidative harm [28].

    When C2C12 cells reached 70% confluence, development medium was switched to myogenic
    differentiation medium supplemented with MIF1, MIF2,
    Ac-MIF1, or Ac-MIF2-NH2 for 3 days. Giemsa staining was carried out and fusion indices have been determined as we
    previously described [52]. C2C12 cells have been grown in progress medium till 70% confluent, after which
    in myogenic differentiation medium (DMEM + 2% FBS + 1% P/S) supplemented with MIF1, MIF2,
    Ac-MIF1 and Ac-MIF2-NH2 for 3 days to promote myoblast differentiation. Scratch assays are normally used to match cell migration parameters similar to velocity, persistence, and polarity
    [31].
    This examine examined 12-weeks of resistance coaching and cystoseira canariensis supplementation on serum
    levels of myostatin and muscle power and body composition in twenty-two untrained males.
    Training consisted of three days per week utilizing 3 units of 6 to 8 repetitions at 85–90% 1 RM.

    The researchers concluded that 12-weeks of
    heavy resistance training and 1200 mg/d of cystoseira
    canariensis supplementation gave the impression to be
    ineffective at inhibiting serum myostatin and increasing muscle strength and mass or
    decreasing fats mass. The rationalization for the
    dramatic results in animals while no observed results in humans in all probability lies in the truth
    that myostatin specific antibodies have been used in the
    animal mannequin, while human fashions use sulfo-polysaccharides
    which are solely advertised to bind to myostatin. Outcomes of this study support this prior report in that
    CSP3 supplementation had no important results on physique composition, coaching variations, or markers of anabolic/catabolic status in resistance-trained males.

    Myostatin is produced by the muscle tissue of the center, and
    injury to the heart causes it to be released into the bloodstream.
    As Soon As within the bloodstream, myostatin reaches the muscle tissue and causes them to weaken over time.
    As a end result, patients with heart illness usually also experience symptoms of
    muscle atrophy (muscle loss) [10]. Bodily exercise, particularly weightlifting, can naturally lower myostatin activity.
    Research show that resistance coaching improves muscle fibers, reduces physique fat, and stimulates skeletal muscle hypertrophy.
    Myostatin inhibitors block or decrease myostatin activity and “unlock” your muscle-building potential.
    By suppressing myostatin expression or its signaling pathways, these inhibitors allow
    your physique to create more muscle fibers and reduce muscle atrophy.

    The variety of myostatin-positive SC–myostatin inhibits the progress
    of SC into the S part of the cell cycle [9]–increased after 2 weeks of immobilization in both
    groups. More studies are wanted to find out the
    connection between disuse-atrophy and myostatin-positive SC.
    However, it was according to the previous study reporting the blunted
    response of the decline within the variety of myostatin-positive
    SC to resistance train in older adults, who
    may have an impaired myogenic capacity in comparability
    with young [34].

    References:

    abuse of Steroids

  2. I can’t mention sufficient times that the higher the quality or
    purity of your Anavar is, the less of it you’ll
    need to take to get the desired results and outcomes.
    Nevertheless, most girls are likely to discover that Anavar is the one that offers them
    one of the best balance of minimal unwanted effects and exceptional outcomes.
    If the steroid is stopped soon enough, these results should reverse and go
    away.
    Dave Crosland, the founder of Crosland’s Hurt Discount Services, has additionally found testosterone and estrogen ranges
    to be poor in females post-Anavar (24). The primary purpose of post-cycle remedy is to restart endogenous testosterone production. This aids in normalizing hormone levels for optimum physiological and psychological well being,
    as properly as retaining outcomes from a cycle.
    When Anavar was initially released in the marketplace, a basic dose of 5–10 mg
    per day was widespread. When Anavar (oxandrolone) was first produced, it was legal to purchase
    for bodybuilding purposes. Doctors would prescribe
    it to folks wanting larger muscular tissues, extra energy, or to burn extra fat.

    Anavar and Winstrol possess many similarities, with both decreasing fats mass
    and water retention while rising lean muscle mass. As I’ve mentioned before, women can benefit more from Anavar by itself than man,
    however, a male can enhance their results by stacking
    Anavar with varied different anabolic steroids. So plenty of the Anavar earlier than and after pictures that you just see on the web might have been individuals who have maximized their results even further by stacking Anavar with different
    steroids. For instance, somebody may stack Anavar with one thing like Clenbuterol as that would give them enhanced results
    in how much fats they might lose.
    Due to Anavar’s gentle androgenic rating, it does not sometimes produce virilization unwanted effects in ladies when taken in low to average doses.
    Generally, Anavar ends in lean muscle gains and improved
    muscle definition. However, the extent of transformation is
    decided by components similar to particular person genetics, diet, and workout routine.
    Anavar, a preferred anabolic steroid also known as Oxandrolone, has
    been broadly used for its muscle-building and fat-loss promoting
    properties. However, like any medicine, it comes with its personal
    set of potential unwanted effects. In this section,
    we’ll talk about both the short-term unwanted effects and
    the long-term health implications of Anavar use.

    We have had sufferers report significant energy results on Anavar, even when consuming low energy.
    This can be why powerlifters usually administer Anavar prior to a contest for maximum strength with out important
    weight achieve. Some frequent side effects include liver
    toxicity, pimples, hair loss, and elevated cholesterol levels.
    Women can also experience virilization, which includes signs such as deepening of the voice, facial hair growth, and enlargement of the clitoris.
    It’s essential to seek the guidance of a medical
    professional before beginning an Anavar cycle to reduce these risks.
    During a chopping cycle, customers sometimes take Anavar for 5 to 8 weeks, with dosages
    starting from 10mg to 50mg every day for males and a pair of.5mg to 10mg daily for women.
    In particular, liver harm is a notable concern when utilizing Anavar, encompassing the potential for cholestatic
    liver harm, liver tumors, and numerous types of hepatic dysfunction. Anavar has a half-life of roughly 9 hours, which
    implies it stays in your system for roughly hours.
    Nonetheless, it may be detected in drug
    checks for as a lot as 3-4 weeks after the final dose.
    One Other research, printed within the Journal of Burn Care and Rehabilitation, evaluated the results of Anavar in burn sufferers.
    The researchers discovered that Anavar helped to protect
    lean body mass and enhance muscle function in sufferers with
    extreme burns. As we prolong our scope towards long-term impacts, the image tends to get clearer
    with Oxandrolone making more of a significant mark.
    With its energy enhancing and muscle preserving traits, the compound can lead to long-lasting enhancements for users.

    The largest concern we see with the addition of trenbolone is a spike in blood strain. This
    is as a outcome of it does not convert to estrogen and thus can skew ldl cholesterol ratios.
    Taking 4 grams of fish oil per day has helped some of our patients stabilize their blood
    pressure (3). Trenbolone, like testosterone, is injectable;
    thus, there are not any obvious damaging effects on the liver with this cycle.

    We have also discovered Anavar to increase T3
    (triiodothyronine) levels (1), whereas enhancing insulin sensitivity, resulting in a reduction in subcutaneous and visceral fats.
    Thus, females can take benefit of a simultaneous muscle-building and
    fat-burning effect. T3 is a thyroid hormone that has been proven to be a
    powerful fat-burning hormone.
    Lewis’s credibility within the bodybuilding community adds weight to the
    endorsement of Anavar as a useful tool in attaining lean muscle gains without compromising health.
    Anavar is often stacked with other compounds to maximize outcomes and minimize side effects.
    Common stacks embrace testosterone for men or low doses of
    different anabolic steroids for girls. It is crucial to remember
    that Oxandrolone is a extremely regarded and extensively used treatment known for its positive impact on patients affected by numerous medical situations.

    To forestall additional liver damage, Anavar
    should not be used with hepatotoxic substances like alcohol.
    In addition, users mustn’t use Anavar if their liver is
    already infected or injured, since this may cause extra hurt.
    As A End Result Of Anavar is a c-17 alpha-alkylated steroid, alanine aminotransferase (ALT) and aspartate aminotransferase (AST) levels
    could be anticipated to rise. In the game of bodybuilding, when veins are visible just beneath the skin’s floor, this is known as vascularity.

    References:

    risks of Taking steroids

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