Harvard Neuroscientists Explore the Science of Acupuncture

Acupuncture is a traditional Chinese technique that has been used for millennia to treat chronic pain and other health problems associated with inflammation, yet the scientific basis of the technique remains poorly understood.

This article is a repost which originally appeared on SciTechDaily
 
Edited for content and readability - Images sourced from Pexels 
DOI: 10.1038/s41586-021-04001-4

Now, a team of researchers led by neuroscientists at Harvard Medical School has elucidated the underlying neuroanatomy of acupuncture that activates a specific signaling pathway.

In a study conducted in mice and published October 13, 2021, in Nature, the team identified a subset of neurons that must be present for acupuncture to trigger an anti-inflammatory response via this signaling pathway.

The scientists determined that these neurons occur only in a specific area of the hindlimb region—thus explaining why acupuncture in the hindlimb works, while acupuncture in the abdomen does not.

“This study touches on one of the most fundamental questions in the acupuncture field: What is the neuroanatomical basis for body region, or acupoint, selectivity?” said lead investigator Qiufu Ma, HMS professor of neurobiology at Dana-Farber Cancer Institute.

One area of particular interest to the research team is the so-called cytokine storm—the rapid release of large quantities of cytokines that frequently drives severe, systemic inflammation, and can be triggered by many things, including COVID-19, cancer treatment, or sepsis.

“This exuberant immune response is a major medical problem with a very high fatality rate of 15 percent to 30 percent,” Ma said. Even so, drugs to treat cytokine storm are lacking. (https://mojokc.com/)

Adapting an ancient technique to treat aberrant inflammation

In recent decades, acupuncture has been increasingly embraced in Western medicine as a potential treatment for inflammation.

In this technique, acupoints on the body’s surface are mechanically stimulated, triggering nerve signaling that affects the function of other parts of the body, including organs.

In a 2014 study, researchers reported that electroacupuncture, a modern version of traditional acupuncture that uses electrical stimulation, could reduce cytokine storm in mice by activating the vagal-adrenal axis—a pathway wherein the vagus nerve signals the adrenal glands to release dopamine.

In a study published in 2020, Ma and his team discovered that this electroacupuncture effect was region specific: It was effective when given in the hindlimb region, but did not have an effect when administered in the abdominal region. The team hypothesized that there may be sensory neurons unique to the hindlimb region responsible for this difference in response.

In their new study, the researchers conducted a series of experiments in mice to investigate this hypothesis. First, they identified a small subset of sensory neurons marked by expression of the PROKR2Cre receptor. They determined that these neurons were three to four times more numerous in the deep fascia tissue of the hindlimb than in the fascia of the abdomen.

Then the team created mice that were missing these sensory neurons. They found that electroacupuncture in the hindlimb did not activate the vagal-adrenal axis in these mice. In another experiment, the team used light-based stimulation to directly target these sensory neurons in the deep fascia of the hindlimb.

This stimulation activated the vagal-adrenal axis in a manner similar to electroacupuncture. “Basically, the activation of these neurons is both necessary and sufficient to activate this vagal-adrenal axis,” Ma said.

In a final experiment, the scientists explored the distribution of the neurons in the hindlimb. They discovered that there are considerably more neurons in the anterior muscles of the hindlimb than in the posterior muscles, resulting in a stronger response to electroacupuncture in the anterior region.

“Based on this nerve fiber distribution, we can almost precisely predict where electrical stimulation will be effective and where it will not be effective,” Ma explained.

Together, these results provide “the first concrete, neuroanatomic explanation for acupoint selectivity and specificity,” Ma added. “They tell us the acupuncture parameters, so where to go, how deep to go, how strong the intensity should be.”

He noted that while the study was done in mice, the basic organization of neurons is likely evolutionarily conserved across mammals, including humans.

However, an important next step will be clinical testing of electroacupuncture in humans with inflammation caused by real-world infections such as COVID-19. Ma is also interested in exploring other signaling pathways that could be stimulated by acupuncture to treat conditions that cause excessive inflammation.

“We have a lot of tough chronic diseases that still need better treatments,” he said, such as inflammatory bowel syndrome and arthritis. Another area of need, he added, is excessive immune reactions that can be a side effect of cancer immunotherapy.

Ma hopes that his research will ultimately advance scientific understanding of acupuncture and provide practical information that can be used to improve and refine the technique.

Peyronie’s Disease and Your Sex Life: 7 Things to Know

7 Ways Peyronie’s Disease Can Affect Your Sex Life

Medically reviewed by Joseph Brito III, MD — Written by Cathy Lovering on February 19, 2021

This article is a repost which originally appeared on Healthline

Edited for content

Peyronie’s disease is when plaques (scar tissue) form under the skin of the penis and cause it to bend. Living with this condition often includes pain and changes to sexual function that can affect personal intimacy, your relationships, and mental health.

Understanding the ways Peyronie’s disease can affect your sex life and partner can help you know what to expect from the disease, along with how treatment options can help.

Here are seven things to know about Peyronie’s disease and sex.

1. Getting and keeping an erection can be challenging

Erectile dysfunction is more common among people with Peyronie’s disease. A 2020 study on 656 men who were receiving care at a urology clinic in Brazil found that nearly 60 percent of men with Peyronie’s disease had erectile dysfunction, compared with 46 percent of men without the condition.

There are a few possible reasons for the connection between Peyronie’s disease and erectile dysfunction. For some, the scarring can make it difficult to get an erection.

Erections can also be challenging if the nerves or blood vessels of the penis have been damaged by inflammation or trauma to the penis, which is associated with Peyronie’s disease.

Many people living with Peyronie’s experience anxiety and depression because of the condition. These feelings can also lead to challenges with sexual function, so the symptoms often compound each other.

Finally, pain (especially during the active phase of the disease) can contribute to erectile dysfunction for some people with Peyronie’s.

2. Your partner may experience pain and discomfort

Peyronie’s disease often causes pain during erections. But that condition doesn’t only cause pain to those living with it — it can also make sex uncomfortable for their partners.

A 2020 study found that nearly half of the female sexual partners of men with the condition experienced at least moderate pain or discomfort during vaginal intercourse.

In some cases, couples couldn’t engage in certain sexual activities they enjoyed before the onset of Peyronie’s.

With that being said, the appearance of your penis might not be as much of an issue to your partner. The research found that nearly 60 percent of men with Peyronie’s disease were very or extremely bothered by how their erect penis looks, while just 20 percent of their female sexual partners felt the same way.

3. Communication can help couples cope

While it can be difficult to talk about Peyronie’s disease, communication is key to maintaining intimacy with your partner and finding new ways to be sexual.

Here are some ways to make the conversation easier, according to the Association of Peyronie’s Disease Advocates (APDA):

  • Discuss the condition and its effects over several conversations. Don’t feel like you have to cover everything in one sitting.
  • Your feelings and symptoms can change over time, so you may need to revisit topics in future conversations. Try to be honest about what you’re going through.
  • Make sure the conversation is a dialogue, not a monologue. As much as you share your concerns, listen to your partner express how your condition is affecting them, as well.

The APDA also encourages people with Peyronie’s disease to involve their partners in exploring treatment options and going to doctor’s appointments.

4. Couples may need to explore new forms of intimacy

If Peyronie’s disease is making it challenging to have sex the way you’re used to, it might be time to explore new techniques.

Partners can use different positions or explore other forms of intimacy and pleasure besides intercourse to achieve satisfaction.

Speaking with a sex therapist or counselor can help both people in the relationship share their sexual needs and desires and work through challenges in the relationship.

5. Over-the-counter (OTC) medication can provide pain relief

Treatments for Peyronie’s disease, which range from injections to surgery and penile implants, usually have the goal to reduce curvature and improve sexual function.

However, not all people with the condition need medical treatments. If pain is your main symptom, OTC pain relievers, such as nonsteroidal anti-inflammatory drugs (NSAIDs) like ibuprofen (Advil) or naproxen (Aleve), may be all you need to have a more comfortable erection.

6. Treatments can boost sexual satisfaction

There are a number of surgical and nonsurgical treatments for Peyronie’s disease. While they’re typically focused on reversing curvature and breaking up plaques, some treatments have the added benefit of boosting satisfaction for partners of people with the condition.

A 2020 review of small studies found that 70 percent of female partners of men with Peyronie’s disease who were treated with collagenase clostridium histolyticum injections experienced higher sexual satisfaction.

Female partner sexual satisfaction also climbed by 34 percent to 88 percent when men were treated with penile plication, 90 to 100 percent after they underwent plaque incision or partial excision with grafting, and 40 to 75 percent after penile prosthesis implantation (a treatment typically reserved for people with severe Peyronie’s disease and erectile dysfunction).

It’s important to note that available research only surveyed women who were intimate with men with Peyronie’s disease, so further study is needed to determine how the condition and treatments can affect non-female partners.

7. Talking with others can make you feel better

The psychological impacts of Peyronie’s disease can affect your emotional well-being, as well as your ability to be intimate.

According to APDA, the condition can change the way a person sees themself and hurt their self-confidence.

People with Peyronie’s disease may avoid intimacy, lose interest in sex, and withdraw emotionally. This can cause a range of psychological challenges for both people in the relationship.

Overcoming emotional and social isolation can help reduce the impact of the condition on your sex life and overall well-being. Consider talking with others who are living with the condition or joining a support group.

A mental health professional, such as a psychologist or a therapist, can also give you a safe space to work through concerns and find ways to cope.

Takeaway

Peyronie’s disease can make a big impact on a person’s sex life, both due to the physical symptoms and the emotional impacts of the condition.

The condition can also make an impact on your partner’s comfort and satisfaction during sex.

Exploring treatment options, having open and honest conversations, and seeing a sex therapist are some of the ways to reduce the effects of Peyronie’s disease on intimacy.

You may also consider joining a support group to connect with others who have the condition.

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